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Небесная энциклопедия

Космические корабли и станции, автоматические КА и методы их проектирования, бортовые комплексы управления, системы и средства жизнеобеспечения, особенности технологии производства ракетно-космических систем

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Мониторинг СМИ

Мониторинг СМИ и социальных сетей. Сканирование интернета, новостных сайтов, специализированных контентных площадок на базе мессенджеров. Гибкие настройки фильтров и первоначальных источников.

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Форма поиска

Поддерживает ввод нескольких поисковых фраз (по одной на строку). При поиске обеспечивает поддержку морфологии русского и английского языка
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Применить Всего найдено 1825. Отображено 198.
07-01-1985 дата публикации

Сорбент для хроматографии оптических изомеров аминокислот

Номер: SU1132966A1
Принадлежит:

СОРБЕНТ ДЛЯ ХРОМАТОГРАФИИ ОПТИЧЕСКИХ ИЗОМЕРОВ АМИНОКИСЛОТ на основе кремнезема, ;содержащего, на поверхности химически привитые ai«иокислотные группы, отличающийся тем, что, с целью увеличения селективности хроматографического разделения, он содерясит аминокислотные группы формулы :-(Й2Ь Н-иН2 1 -СН-С0011 . ИНг при их поверхностной концентрации 0,7-1,2.групп/нм.

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07-07-2005 дата публикации

PURIFICATION OF IMMUNOGLOBULINS

Номер: CA0002549923A1
Принадлежит:

The present invention relates to a separation matrix comprised of a porous support to which ligands have been immobilised, wherein said ligands comprise at least one aliphatic sulphonamide. The nitrogen of the sulphonamide may be a secondary or tertiary amine. The invention also relates to a chromatography column that contains the described separation matrix, as well as to a method of isolating immunoglobulin-like compounds by adsorption to a separation matrix that comprises aliphatic sulphonamide ligands.

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27-07-1993 дата публикации

CHROMATOGRAPHIC MATERIAL

Номер: CA0001320718C
Принадлежит: CHROMATOCHEM INC, CHROMATOCHEM, INC.

Chromatographic material having the general formula SB-X-Y-L where S is a solid support, B is a binding group, X is a substantially non-ionic hydrophilic organic spacer, Y is a coupling group and L is an affinity ligand. The chromatographic material is substantially free of non specific adsorption and is stable at high pH.

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16-11-2006 дата публикации

AFFINITY ADSORBENTS FOR FACTOR VIII AND VON WILLEBRAND'S FACTOR

Номер: CA0002607858A1
Принадлежит:

For the separation, removal, isolation, purification, characterisation, identification or quantification of Factor VIII, von Willebrand's Factor or a protein that is a analogue of either, an affinity adsorbent is used that is a compound of formula (II) wherein one X is N and the other is N, C-C1 or C-CN; A is a support matrix, optionally linked to the triazine ring by a spacer; Y is O, S or NR2; Z is O, S or N-R3; R2 and R3 are each H, C1-6 alkyl, C1-6 hydroxyalkyl, benzyl or .beta.-phenylethyl; B and W are each an optionally substituted hydrocarbon linkage containing from 1 to 10 carbon atoms; D is H, OH or a primary amino, secondary amino, tertiary amino, quaternary ammonium, imidazole, guanidino or amidino group; or B-D is -CHCOOH-(CH2)3-4-NH2; and R7 is a group bearing a positive charge at neutral pH.

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14-02-2013 дата публикации

SEPARATION MATERIAL COMPRISING SACCHARIDE LIGANDS

Номер: CA0002842710A1
Принадлежит:

The present disclosure relates to a separation material comprising a saccharide that is bound via a linker to a matrix for enabling the separation of substances from a liquid that selectively bind to saccharide moieties, to a method for preparing such material, to a method for separating substances from a liquid that selectively bind to saccharides, and to a device comprising a separation material for separating substances from a liquid that selectively bind to saccharides.

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02-08-2005 дата публикации

METHODS FOR THE PREPARATION OF RESINS WITH LIGANDS ATTACHED THERETO THROUGH A LINKING GROUP COMPRISING SULFIDE, SULFOXIDE, SULFONE OR SULFONATE FUNCTIONALITY

Номер: CA0002240064C
Принадлежит: MASSEY UNIVERSITY, UNIV MASSEY

Methods for the preparation of chromatographic resins comprising a support matrix having ligands capable of binding a target compound covalently attached thereto through a linking group comprising sulfide, sulfoxide, sulfone or sulfonate functionality. Specifically, in the disclosed methods, a support matrix comprising ethylenically unsaturated functionality is contacted with a thiol group or a bisulfite salt under free radical reaction conditions. In the case of the reaction wit h the thiol group, subsequent optional oxidation of the sulfide to the sulfone or sulfoxide functionality may occur.

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26-08-2004 дата публикации

RIGID COMPOSITION FOR SELECTIVE ADSORPTION FROM COMPLEX MIXTURES

Номер: EA0200400310A1
Автор:
Принадлежит:

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06-08-2014 дата публикации

Sorbent comprising on its surface an aromatic ring system having an anionic or deprotonizable group for the purification of organic molecules

Номер: CN103974764A
Принадлежит:

The present invention relates to a sorbent comprising a solid support material, the surface of which comprises a residue of a general formula (I), wherein the residue is attached via a covalent single bond to a functional group on the surface of either the bulk solid support material itself or of a polymer film on the surface of the solid support material. Furthermore, the present invention relates to the use of the sorbent according to the invention for the purification of organic molecules, in particular pharmaceutically active compounds, preferably in chromatographic applications.

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19-08-2004 дата публикации

CUCURBITURIL-BONDED SILICA GEL

Номер: KR20040072810A
Принадлежит:

PURPOSE: Provided is a silica gel covalent-bonded to cucurbituril or a silica gel covalent-bonded to the cucurbituril and cyclodextrin, which is used for a stationary phase of a column filler or a filter for removing pollution material. CONSTITUTION: The cucurbituril represented by the formula 1 is covalent-bonded to a modified silica gel represented by the formula 2. And the cucurbituril represented by the formula 1 and the cyclodextrin represented by the formula 7 are covalent-bonded to the modified silica gel represented by the formula 2. In the formula, n is an integer of 4-20, R1 is independently a C1-C20 alkenyloxy of which the terminal is an unsaturated bond, a carboxy alkylsulfanyloxy having a C1-C20 alkyl, a carboxy alkyloxy having a C2-C8 alkyl, an aminoalkyloxy having a C2-C8 alkyl, or a hydroxyalkyloxy having a C2-C8 alkyl, R2 is an alkylthiol having a C3-C8 alkyl, an alkyl amine having a C3-C8 alkyl, or an epoxy alkyloxy alkyl having a C3-C8 alkyl, an isocyanate having a C3 ...

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10-08-2006 дата публикации

PACKING MATERIAL FOR ION CHROMATOGRAPHY

Номер: WO2006083022A1
Принадлежит:

The present invention relates to a packing material for ion chromatography, wherein a quaternary ammonium base represented by the following formula (1) is bonded to the substrate directly or through a spacer: wherein R1 represents a group having at least one olefinic double bond or conjugated double bond, each R2 and R3 independently represents an organic residue which may be the same with or different from R1; and separating equipment for chemical substances and a separating method using the packing material. The packing material for ion chromatography, separating equipment for chemical substances and a separating method using the packing material of the present invention, enable to sufficiently separate seven standard inorganic anions and three halogen oxide anions in either of the conductometric detection or ultraviolet detection by postcolumn derivatization while preventing increase in the pressure and imposing no limitations on the measurement temperature or flow rate of mobile phase ...

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11-01-2007 дата публикации

[1, 2, 4] TRIAZOLO [1, 5-A] PYRIMIDINE DERIVATIVES AS CHROMATOGRAPHIC ADSORBENT FOR THE SELCTIVE ADSORPTION OF IGG

Номер: WO2007004954A1
Принадлежит:

The present invention relates to a chromatographic adsorbent for selectively adsorbing IgG, comprising the following formula (I) and its corresponding enol-form, wherein X represents O, S, or NH; R1 represents H, C1-6 alkyl, C1-6alkoxy, C1-6 alkoxy-C1-6 alkyl, Ar, -C(O)NHR3, -C(O)-R3 or halo; R2 represents H, C1-3 alkyl or halo; R3 represents H, C1-6 alkyl, C1-6 alkoxy, C1-6 alkoxy-C1-6alkyl or Ar; n represents 0, 1, 2 or 3; Y represents a carrier. The present invention also relates to a method of producing said adsorbent as well as use thereof for separating substances by affinity chromatography.

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10-07-2008 дата публикации

HIGH-PERFORMANCE CHROMATOGRAPHIC COLUMNS CONTAINING ORGANIC OR COMPOSITE POLYMERIC MONOLITHIC SUPPORTS AND METHOD FOR THEIR PREPARATION

Номер: WO2008081496A1
Принадлежит:

The invention concerns high-performance chromatographic columns containing polymeric monolithic supports with continuous bimodal porosity, suitable for the separation and/or purification of organic compounds of low, medium and high molecular weight, and bio-organic compounds such as pep¬ tides, proteins, oligo- and polynucleotides, oligo- and polysaccharides. The proposed columns include a hollow tubular support made of silica-based amorphous material or internally lined with such material, containing a mono¬ lithic stationary phase having a continuous, porous and rigid polymeric struc¬ ture, wherein such stationary phase covalently bonds onto the internal walls of the said hollow tubular support. The chromatographic efficiency of the column is greater than 50,000 plates per metre. The invention also concerns methods for preparing such monolithic columns with gamma radiation-induced polymerization processes.

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06-10-2011 дата публикации

METHOD FOR ISOLATING AN ANALYTE FROM A SAMPLE FLUID WITH A PROTEIN-REPELLENT HYDROGEL

Номер: WO2011120691A1
Принадлежит:

The present invention relates to a method of the present invention according to which at least one analyte is isolated from a sample fluid containing said at least analyte and at least one protein, comprising the steps of: a) contacting the sample fluid with a protein-repellent hydrogel immobilized on a solid surface to capture said at least one analyte; b) separating the hydrogel obtained in step a); c) optionally washing the hydrogel obtained in step b) with an aqueous solution containing up to ca. 30% by volume of an organic water-miscible solvent; d) contacting the hydrogel obtained in step c) with an aqueous solution containing at least 60% by volume of an organic water-miscible solvent; and e) isolating said at least one analyte obtained in step d); wherein the hydrogel is obtained by co-polymerization of at least one uncharged and polar monomer with at least one hydrophobic monomer and at least one cross-linking monomer.

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05-07-2007 дата публикации

Chromatographic material for the absorption of proteins at physiological ionic strength

Номер: US2007151910A1
Принадлежит:

Ion exchange and hydrophobic interaction chromatographic materials are constructed by tethering a terminal binding functionality to a solid support via a hydrophobic linker. The backbone of the linker typically comprises sulfur-containing moieties. Suitable terminal binding functionalities are tertiary amines, quaternary ammonium salts, or hydrophobic groups. These chromatographic materials possess both hydrophobic and ionic character under the conditions prescribed for their use. The separation of proteins from crude mixtures at physiological ionic strength can be accomplished with a chromatographic material of this type by applying pH or ionic strength gradients, thereby effecting protein adsorption and desorption.

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30-08-2018 дата публикации

SEPARATING AGENT FOR LIQUID CHROMATOGRAPHY, SEPARATION COLUMN, AND METHOD FOR SEPARATING AND PURIFYING BIOPOLYMER USING THEM

Номер: US20180243725A1
Принадлежит:

In order to provide a separating agent for liquid chromatography that is able to separate a protein using target characteristics as an index while retaining the original steric structure, the separating agent for liquid chromatography is equipped with a substrate, a recognition site including a compound that operates by recognizing characteristics of biopolymers such as proteins, and a spacer that bonds the recognition site to the substrate, wherein the spacer has an effective length to enable the recognition site to operate by reaching deep portions of the steric structure of a target biopolymer. 1. A separating agent for liquid chromatography comprising:a substrate;a recognition site including a compound that operates by recognizing characteristics of biopolymers; anda spacer that bonds the recognition site to the substrate,wherein the spacer has an effective length to enable the recognition site to operate by reaching deep portions of the steric structure of a target biopolymer.2. The separating agent for liquid chromatography according to claim 1 , wherein the length of the spacer is not less than 1 nm and not more than 50 nm.3. The separating agent for liquid chromatography according to claim 1 , wherein the spacer includes a polymer equal to or greater than a dimer.4. The separating agent for liquid chromatography according to claim 1 , wherein the polymer serving as the spacer contains an ether bond claim 1 , an ester bond claim 1 , an amide bond claim 1 , a urea bond claim 1 , or a urethane bond.5. The separating agent for liquid chromatography according to claim 1 , wherein the recognition site contains an organic π electron system compound.6. The separating agent for liquid chromatography according to claim 1 , wherein the recognition site includes fullerene.7. The separating agent for liquid chromatography according to claim 1 , wherein the substrate contains at least one or a plurality of compounds selected from a group containing metal oxides claim 1 , ...

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19-08-2009 дата публикации

Improved chromatography resin, and methods and devices related thereto.

Номер: EP2090361A1
Принадлежит:

The invention relates to the field of analytical and preparative chemistry. Among others, it relates to an improved chromatographic resin and to means and methods involving use of the resin for the (on-line) clean up of complex test samples, such as biological samples. Provided is a chromatographic resin comprising a rigid polymer that is functionalized with at least one ligand capable of binding to a molecule of interest, wherein said ligand is covalently attached to the polymer via a small hydrophilic moiety based on a compound having 1-10 C-atoms and comprising a multiplicity of hydrophilic groups.

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01-01-2020 дата публикации

MULTIMODAL ANION EXCHANGE MATRICES

Номер: EP2919902B1
Принадлежит: GE Healthcare BioProcess R&D AB

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20-07-2008 дата публикации

СПОСОБ ВЫДЕЛЕНИЯ БЕЛКА

Номер: RU2007100351A
Принадлежит:

... 1. Способ выделения белков из раствора, содержащего указанные белки, где указанный раствор выбран из группы, состоящей из: сырой плазмы крови, сыворотки крови, криосупернатанта, полученного из плазмы, фракционированной человеческой плазмы, криоосадка, полученного из плазмы, и рекомбинантных бульонов, где указанный способ включает: (i) получение твердой разделяющей среды, имеющей формулу: M-S-L, где M представляет собой матриксный остов, S представляет собой необязательное спейсерное плечо и L представляет собой лиганд, который является меркаптоникотиновой кислотой; (ii) контактирование указанной твердой разделяющей среды с указанным раствором, так что по меньшей мере один из указанных белков обратимо связывается с указанной твердой разделяющей средой; (ii) выполнение по меньшей мере одной стадии элюирования для селективного элюирования из твердой разделяющей среды по меньшей мере одной белковой фракции. 2. Способ по п.1, где раствором является сырая плазма крови. 3. Способ по п.1 или 2, ...

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15-11-1992 дата публикации

METHOD OF PRODUCING SORBENT FOR LIQUID CHROMATOGRAPHY

Номер: RU1775662C
Автор:
Принадлежит:

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15-06-2005 дата публикации

Affinity adsorbents for fibrinogen

Номер: GB0000509442D0
Автор:
Принадлежит:

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15-06-2005 дата публикации

Affinity adsorbents for factor VIII and von willebrand's factor

Номер: GB0000509443D0
Автор:
Принадлежит:

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15-08-2005 дата публикации

PROCEDURE FOR THE ADSORPTION/CSEPARATION

Номер: AT0000300346T
Принадлежит:

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15-04-2008 дата публикации

AUFREINIGUNG OF IMMUNGLOBULINEN

Номер: AT0000391729T
Принадлежит:

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26-08-2004 дата публикации

Silica gel bonded with cucurbiturils

Номер: AU2004212090A1
Принадлежит:

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25-08-1998 дата публикации

An adsorption/separation method and a medium for adsorption/separation

Номер: AU0006009898A
Принадлежит:

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08-03-2007 дата публикации

MANUFACTURE OF CHROMATOGRAPHY MATRICES

Номер: CA0002620385A1
Принадлежит:

The present invention relates to a method of manufacturing a chromatography matrix comprising providing a polysaccharide carrier comprising available hydroxyl groups; and reacting said hydroxyl groups with vinyl sulphonate to provide a sulphonate-functionalized (S-functionalized) cation exchanger. The hydroxyl groups of the carrier may be hydroxyls of the agarose polymer; or alternatively they may be provided on extenders such as polyhydroxyfunctional polymers. In one embodiment, the carrier is made of agarose with improved flow pressure properties.

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26-03-2015 дата публикации

SWITCHABLE MATERIALS, METHODS AND USES THEREOF

Номер: CA0002924633A1
Принадлежит:

The present application provides a composite material that comprises a solid and solid-supported non-polymeric switchable moiety, wherein the switchable moiety comprises a functional group that is switchable between a first form and a second form, said first form being neutral and hydrophobic, and said second form being ionized and hydrophilic. The composite material converts to, or is maintained in, said second form when the switchable moiety is exposed to CO2 at amounts sufficient to maintain the ionized form. The composite material converts to, or is maintained in, said first form when CO2 is removed or reduced to an amount insufficient to maintain the ionized form. CO2 is removed or reduced by exposing the composite material to heat and/or a flushing inert gas such as N2, Ar, or air. Envisioned uses of these composite materials includes removing water from non-aqueous solvents, removing water vapour from gaseous mixtures, and cleaning industrial reaction vessels and/or pipelines.

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01-08-2006 дата публикации

HYDROPHOBIC CHROMATOGRAPHIC RESINS WITH IONIZABLE GROUPS

Номер: CA0002193867C
Принадлежит: MASSEY UNIVERSITY, UNIV MASSEY

Disclosed are resins, resin-protein/peptide complexes and methods for purifying proteins and peptides using said resins. The resins described herein are useful for the binding of a selected protein or peptide , particularly from an aqueous medium such as a fermentation broth, by hydrophobic interactions between the resin and the selected protei n or peptide. The resin is characterized by the fact that it contains ionizable ligands and/or functionalities which are uncharged at the pH of binding the target protein or peptide, thereby facilitating hydrophobic interactions, and charged at the pH of desorption, thereby disrupting the established hydrophobic interaction between the resin and the target protein or peptide. More particularly, the present invention is directed to the use of the described resins in the purification of recombinant enzyme products such as proteases, for example, chymosin or subtilisin.

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24-07-2017 дата публикации

돌연변이된 이뮤노글로불린-결합 폴리펩티드

Номер: KR1020170085502A
Принадлежит:

... 본 발명은 적어도 서열식별번호: 4-7의 위치 42에 해당하는 위치의 알라닌 잔기가 아르기닌으로 돌연변이되어 있고/거나, 적어도 서열식별번호: 4-7의 위치 37에 해당하는 위치의 아스파르트산 잔기가 글루탐산으로 돌연변이되어 있는, 서열식별번호: 1, 서열식별번호: 2, 서열식별번호: 3, 서열식별번호: 4, 서열식별번호: 5, 서열식별번호: 6, 서열식별번호: 7, 서열식별번호: 8, 서열식별번호: 26 또는 서열식별번호: 27에 의해 정의되는 바와 같은 스태필로코쿠스 단백질 A (SpA) Fc-결합 도메인의 돌연변이를 포함하는 향상된 알칼리 안정성의 Fc-결합 폴리펩티드에 관한 것이다.

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04-12-2008 дата публикации

COMPOSITIONS USEFUL AS CHROMATOGRAPHY STATIONARY PHASES

Номер: WO2008147717A4
Принадлежит:

The current invention provides compositions, which are useful as stationary phases for a variety of chromatographic applications, such as high performance liquid chromatography (HPLC). The compositions include a substrate (e.g., silica gel), covalently bound to a compound, which includes both a hydrophobic moiety and a hydrophilic moiety, which is preferably a 1,2-diol moiety. The hydrophobic moiety is sufficiently hydrophobic for the compositions to exhibit reversed phase characteristics and typically incorporates at least 5 carbon atoms in sequence. Based on having both hydrophilic and hydrophobic functionalities, the new stationary phases exhibit unique chromatographic properties. For example, these media can be used in either hydrophilic (HILIC) mode, in which the mobile phase includes a high percentage of an organic solvent, or in reversed phase mode, in which the mobile phase contains a higher percentage of an aqueous solvent. The current invention also provides methods of making ...

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08-03-2007 дата публикации

MANUFACTURE OF CHROMATOGRAPHY MATRICES

Номер: WO000002007027139A1
Принадлежит:

The present invention relates to a method of manufacturing a chromatography matrix comprising providing a polysaccharide carrier comprising available hydroxyl groups; and reacting said hydroxyl groups with vinyl sulphonate to provide a sulphonate-functionalized (S-functionalized) cation exchanger. The hydroxyl groups of the carrier may be hydroxyls of the agarose polymer; or alternatively they may be provided on extenders such as polyhydroxyfunctional polymers. In one embodiment, the carrier is made of agarose with improved flow pressure properties.

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06-08-1998 дата публикации

AN ADSORPTION/SEPARATION METHOD AND A MEDIUM FOR ADSORPTION/SEPARATION

Номер: WO1998033572A1
Принадлежит:

A method for adsorption of a substance from a liquid sample on a fluidized bead or stirred suspension, in which the beads used comprise a base matrix and exhibit a structure having affinity to the substance, characterized in that the structure is covalently bound to the base matrix via an extender. Populations of beads in which the beads contain a filler incorporated in a base matrix and an extender are also described.

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29-04-2004 дата публикации

AFFINITY ADSORBENTS FOR IMMUNOGLOBULINS

Номер: WO2004035199A1
Принадлежит:

Use of a compound of formula (I) wherein R1 and R2 are the same or different and are each optionally substituted alkyl or aryl; and R3is a solid support optionally attached via a spacer; for the affinity binding of an immunoglobulin or fragment thereof.

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18-08-2020 дата публикации

Chromatographic materials for the separation of unsaturated molecules

Номер: US0010744484B2

The present disclosure relates to a method of separating a compound of interest, particularly unsaturated compound(s) of interest, from a mixture. The compound is separated using a column having a chromatographic stationary phase material for various different modes of chromatography containing a first substituent and a second substituent. The first substituent minimizes compound retention variation over time under chromatographic conditions. The second substituent chromatographically and selectively retains the compound by incorporating one or more aromatic, polyaromatic, heterocyclic aromatic, or polyheterocyclic aromatic hydrocarbon groups, each group being optionally substituted with an aliphatic group. In some examples, the present disclosure can include a chromatographic system having a chromatographic column having a stationary phase with a chromatographic substrate containing silica, metal oxide, an inorganic-organic hybrid material, a group of block copolymers, or a combination ...

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29-10-2020 дата публикации

SUPERFICIALLY POROUS PARTICLES AND METHODS FOR FORMING SUPERFICIALLY POROUS PARTICLES

Номер: US20200338528A1
Принадлежит:

Superficially porous particles are disclosed, each including a solid core and a layered porous shell. The layered porous shell includes a porous inner layer and at least one porous outer layer, a shell skeleton thickness greater than 1 nm, and constitutes from 10 vol % to 90 vol % of the plurality of superficially porous particles. The porous inner layer includes an inner layer thickness of less than 300 nm. The at least one porous outer layer includes a cumulative outer layer thickness ranging from 1 to 100 times the inner layer thickness, a predominately radial pore orientation, and an outer layer pore structure which is more organized than the inner layer pore structure. A layer-by-layer process for forming a plurality of superficially porous particles with layered structure is disclosed. A post-modification process for preparing a plurality of chromatographically enhanced superficially porous properties is also disclosed.

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09-09-2015 дата публикации

SURFACE MODIFICATION OF POROUS BASE SUPPORTS

Номер: EP2914377A1
Принадлежит:

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10-03-2021 дата публикации

POROUS CYCLODEXTRIN POLYMERIC MATERIALS

Номер: EP3789451A1
Принадлежит:

A nucleophilic substitution reaction to crosslink cyclodextrin (CD) polymer with rigid aromatic groups, providing a high surface area, mesoporous CD-containing polymers (P-CDPs). The P-CDPs can be used for removing organic contaminants from water. By encapsulating pollutants to form well-defined host-guest complexes with complementary selectivities to activated carbon (AC) sorbents. The P-CDPs can rapidly sequester pharmaceuticals, pesticides, and other organic micropollutants, achieving equilibrium binding capacity in seconds with adsorption rate constants 15-200 times greater than ACs and nonporous CD sorbents. The CD polymer can be regenerated several times, through a room temperature washing procedure, with no loss in performance.

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20-12-2006 дата публикации

PREPARATION OF POROUS INORGANIC/ORGANIC HYBRID PARTICLES FOR CHROMATOGRAPHIC SEPARATIONS

Номер: EP0001733786A1
Принадлежит:

Novel material for chromatographic separations, processes for its preparation, and separations devices containing the chromatographic material are disclosed. In particular, the present invention describes porous inorganic/organic hybrid particles having a chromatographically-enhancing pore geometry, which desirably may be surface modified, and which offer more efficient chromatographic separations than that known in the art.

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10-01-2007 дата публикации

ПЕРФТОРИРОВАННЫЕ СУЛЬФОНИЛГАЛОГЕНИДЫ И АНАЛОГИЧНЫЕ ИМ СОЕДИНЕНИЯ КАК МОДИФИКАТОРЫ ПОЛИМЕРНЫХ ПОДЛОЖЕК

Номер: RU2291146C2

Настоящее изобретение относится к перфторированным сульфонилгалогенидам - модификаторам полимерных подложек - общей формулы где L - компонент связывающей группы; Х - фрагмент, выбранный из группы, состоящей из F, Cl и ОН, причем связанный с подложкой активатор ковалентно связан с твердой или полутвердой подложкой. Описан также способ применения активированных подложек в твердофазном органическом синтезе. 3 н. и 13 з.п. ф-лы, 3 табл.

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10-07-2005 дата публикации

СОРБЕНТ ДЛЯ РАЗДЕЛЕНИЯ ОПТИЧЕСКИХ ИЗОМЕРОВ И СПОСОБ ЕГО ПОЛУЧЕНИЯ

Номер: RU2255802C1

Изобретение относится к сорбентам для хроматографии и может быть использовано для анализа и препаративной очистки оптически активных соединений. Сущность изобретения состоит в том, что разработан новый сорбент для разделения изомеров оптически активных соединений, который в качестве хирального селектора содержит макроциклический гликопептидный антибиотик эремомицин, ванкомицин, ристомицин А, тейкопланин или их агликоны. Разработан способ иммобилизации макроциклических гликопептидных антибиотиков, который заключается в том, что вначале силикагель в водном буферном растворе обрабатывают 3-глицидоксипропилтриалкоксисиланом, а затем в щелочном водном или водно-органическом растворе к силикагелю, модифицированному эпоксигруппами, прививается макроциклический гликопептидный антибиотик, выбранный из ряда: эремомицин, ристомицин А, ванкомицин, тейкопланин или их агликоны. Изобретение позволяет достичь более высоких значений энантиоселективности и упрощает способ получения. 2 н. и 8 з. п. ф-лы, ...

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27-02-2005 дата публикации

ПЕРФТОРИРОВАННЫЕ СУЛЬФОНИЛГАЛОГЕНИДЫ И АНАЛОГИЧНЫЕ ИМ СОЕДИНЕНИЯ КАК МОДИФИКАТОРЫ ПОЛИМЕРНЫХ ПОДЛОЖЕК

Номер: RU2003121311A
Принадлежит:

... 1. Связанный с подложкой активатор, имеющий формулу где L - компонент связывающей группы; Х - фрагмент, выбранный из группы, состоящей из F, Cl, ОН и трехзамещенной силилоксигруппы; причем связанный с подложкой активатор ковалентно связан с твердой или полутвердой подложкой. 2. Связанный с подложкой активатор по п.1, в котором Х - это F. 3. Связанный с подложкой активатор по п.1 или 2, в котором L включает часть, усиливающую действие активатора, выбранную из группы, состоящей из где Y - фрагмент, выбранный из группы, состоящей из химической связи, О, С(O), S и NR1; Z - фрагмент, выбранный из группы, состоящей из химической связи и С(O); R1 - фрагмент, выбранный из группы, состоящей из Н и (С1-С8)алкила; каждый R2 - фрагмент, независимо выбранный из группы, состоящей из водорода, галогена, групп (С1-С8)алкил, (С1 -С8)алкокси, (С1-С8)гетероалкил, (С1-С8)алкилтио, (С1-С8)алкиламино, ди(С1-С8)алкиламино, циано, нитро и (С1-С8)алкилсульфонил; индекс ‘g’ - это целое число, выбранное из группы ...

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15-11-1992 дата публикации

Способ получения сорбента для жидкостной хроматографии

Номер: SU1775662A1
Принадлежит:

Использование: в жидкостной хроматографии для разделения сложных смесей полярных органических веществ. Сущность изобретения: сорбент получают обработкой кремнезема силилирующим агентом при нагревании в среде органического растворителя и дополнительным модифицированием кремнийорганическим модификатором. В качестве силилирующего агента применяют метилвинилдихлорсилан, а в качестве дополнительного модификатора берут силок- сановыйолигомерформулы (С1-.)510}з. где R - радикалы: -СНз: -CeHs; н-СюН21 и реакцию проводят в присутствии инициатора - перекиси , дикумила, причем модификатор и инициатор берут в равных количествах, 2 табл. J ...

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04-07-2018 дата публикации

Materials for hydrophilic interaction chromatography and processes for preparation and use thereof for analysis of glycoproteins and glycopeptides

Номер: GB0002558103A
Принадлежит:

A method of performing hydrophilic interaction liquid chromatography (HILIC) for characterizing a glycosylated proteinaceous sample comprising the steps of; preparing a sample containing the glycosylated proteinaceous sample; providing a HILIC column having an inlet and an outlet, and a stationary phase material; loading the sample on said stationary phase material at a column inlet pressure of no less than 3000 psi and flowing the sample with a mobile phase eluent through the column; and separating the sample from the outlet into one or more fractions. The glycosylated proteinaceous material is preferably a glycosylated monoclonal antibody. The stationary phase preferably comprises a porous material comprising a copolymer comprising at least one hydrophilic monomer and a poly-amide bonded phase. The poly-amide bonded phase is preferably formed of acrylamide monomers. The porous material is preferably fully porous or superficially porous, and preferably comprises pores having an average ...

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28-12-2022 дата публикации

Separation of base metals

Номер: GB0002608230A
Принадлежит:

Use of a separation material comprising picolinic acid ester or picolinic acid amide functional groups immobilised on a solid support to selectively remove nickel (Ni) from an aqueous solution. The aqueous solution may also comprise cobalt (Co), and manganese (Mn) and/or lithium (Li). The functional group may comprise picolinamide. The solid support may be silica, silica-polymer composite and/or an optionally cross-linked methacrylate. The aqueous solution pH may be between 0.5-2.5. A method of selectively removing Ni from an aqueous solution is defined, comprising contacting the solution with a separation material comprising picolinic acid ester or picolinic acid amide functional groups immobilised on a solid support, and methods of chromatographically separating Ni from one or more other metals in an aqueous solution, and Co from Li and/or Mn in an aqueous solution, are also defined. A separation material comprising picolinic acid ester or picolinic acid amide functional groups immobilised ...

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15-03-1997 дата публикации

CHROMATOGRAPHI MATERIAL

Номер: AT0000150176T
Принадлежит:

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15-12-2010 дата публикации

NEW GETRÄGERTE CATALYST SYSTEMS

Номер: AT0000488297T
Принадлежит:

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02-05-2013 дата публикации

Separation matrix

Номер: AU2008279841B2
Принадлежит:

The present invention relates to a separation matrix, which comprises a support; extenders coupled to an outer part of said support; and ligands coupled to said extenders, wherein the part of the support to which the extenders are coupled constitutes less than 50% of the volume of the separation matrix. The invention also embraces a method of preparing such a separation matrix, as well as a process wherein the separation media is used.

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05-08-2004 дата публикации

ALKYL-LINKED NUCLEOTIDE COMPOSITIONS

Номер: CA0002513901A1
Принадлежит:

Alkyl-linked nucleotide compositions and nucleotide affinity media comprising an alkyl-linked nucleotide are provided. The linker is generally a hydrophobic linker that can be a 3, 4, 5, 6, 7, 8, 9, 10, or a longer carbon chain. Also included in the invention are methods for synthesis of an alkyl-linked nucleotide, nucleotide affinity media and methods of use thereof for affinity chromatography and screening methods.

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31-12-1985 дата публикации

ORGANO-METAL MATERIALS

Номер: CA1198723A

Compositions in which organo-mercurial moieties are bound to glass or other inorganic substrates are useful in separating sulfhydryl-containing compounds from mixtures with other compounds, e.g., by affinity chromatography.

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20-06-1990 дата публикации

ENANTIOMERIC SILANES, MODIFIED PACKING MATERIAL, AND USE THEREOF

Номер: CA0002005855A1
Принадлежит:

A compound of formula I (I), wherein R1 is C1-C4alkyl, phenyl or benzyl, R2 is C1-C4alkyl, phenyl or benzyl, a is 0,1 or 2, R3 is linear or branched unsubstituted or OH-substituted C1-C12alkylene or is phenylene, R5 is the divalent radical, diminished by the -CO-O group, of a lactone having a total of 4 to 7 ring members and containing at least one chiral carbon atom and corresponding predominantly to an optically active enantiomeric form, R4 is a direct bond, C1-C4alkyl-CH or CF3-CH, and Y is phenyl, naphthyl, fluorenyl or anthryl, each unsubstituted or substituted by C1-C12alkyl, C1-C12alkoxy, halogen, -CN or -NO2. These compounds are suitable for the preparation of stationary phases for the chromatographic separation of chiral compounds.

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06-08-1998 дата публикации

AN ADSORPTION/SEPARATION METHOD AND A MEDIUM FOR ADSORPTION/SEPARATION

Номер: CA0002280004A1
Принадлежит:

A method for adsorption of a substance from a liquid sample on a fluidized bead or stirred suspension, in which the beads used comprise a base matrix and exhibit a structure having affinity to the substance, characterized in that the structure is covalently bound to the base matrix via an extender. Populations of beads in which the beads contain a filler incorporated in a base matrix and an extender are also described.

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23-12-2003 дата публикации

Purification of immunoglobulins

Номер: SE0000303532D0
Автор:
Принадлежит:

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12-04-2018 дата публикации

NOVEL CHROMATOGRAPHY MEDIA

Номер: WO2018065269A1
Принадлежит:

The present invention relates to a novel chromatography media, more closely a novel IMAC (Immobilized Metal Affinity Chromatography) media. The novel chromatography media comprises a pentaligand and provides high dynamic binding capacity as well as high purity of the sample proteins purified on the media of the invention.

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15-09-2020 дата публикации

Modified Fab region-binding peptide

Номер: US0010774115B2

A first Fab region-binding peptide includes an amino acid sequence selected from the group consisting of SEQ ID NOs: 1 to 5 with substitution of one or more amino acid residues at the 17th position and the 36th position, wherein an acid dissociation pH thereof is shifted to a neutral side. A second Fab region-binding peptide further includes deletion, substitution and/or addition of one or more amino acid residues at positions other than the 17th position and the 36th position. A third Fab region-binding peptide includes an amino acid sequence with a sequence identity of 80% or more to the amino acid sequence of the first Fab region-binding peptide.

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03-08-2017 дата публикации

FILTRATION MATERIAL, FILTRATION FILTER, METHOD FOR MANUFACTURING FILTRATION MATERIAL, FILTRATION METHOD, COPOLYMER, AND METHOD FOR MANUFACTURING COPOLYMER

Номер: US20170216814A1
Принадлежит: TOKYO OHKA KOGYO., LTD.

A filtration material including a silica base material having a group represented by the following general formula (a0-1) [in formula (a0-1), Yarepresents a divalent linking group; Rarepresents a hydrocarbon group which may have a substituent; Rarepresents a hydroxyl group or a hydrocarbon group having 1 to 6 carbon atoms which may have a substituent; nrepresents an integer of 0 to 5; and the symbol “*” represents a valence bond with respect to the silica base material]. 2. The filtration material according to claim 1 , wherein said silica base material is a porous and flexible silica fiber.3. The filtration material according to claim 1 , wherein said silica base material is a silica gel.4. The filtration material according to claim 3 , wherein said silica gel has a particle size of 2 to 50 μm.8. The filtration material according to claim 1 , wherein said filtration material is used for filtering a resist composition or an organic solvent.9. A filtration filter comprising the filtration material according to .10. A filtration method comprising passing a resist composition or an organic solvent through the filtration filter according to to remove impurities in the resist composition or the organic solvent.11. The filtration method according to claim 10 , wherein said impurities are metal components.13. The method for producing a filtration material according to claim 12 , wherein said filtration material is used for filtering a resist composition or an organic solvent.14. The method for producing a filtration material according to claim 12 , wherein said filtration material is a filtration filter.15. A filtration method comprising passing a resist composition or an organic solvent through a filtration material obtained by the method according to to remove impurities in the resist composition or the organic solvent.16. The filtration method according to claim 15 , wherein said impurities are metal components. The present invention relates to a filtration material, a ...

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15-06-2005 дата публикации

Affinity adsorbets for fibrinogen

Номер: GB0000509438D0
Автор:
Принадлежит:

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15-04-2010 дата публикации

POROUS HYBRID PARTICLES FOR CHROMATOGRAPHI SEPARATION

Номер: AT0000464118T
Принадлежит:

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27-02-2003 дата публикации

SOLID COMPOSITIONS FOR SELECTIVE ADSORPTION FROM COMPLEX MIXTURES

Номер: CA0002457730A1
Принадлежит:

The present invention relates to a solid and method useful in separating chemical components in a complex mixture when at least one of the chemical components of the mixture is capable of being selectively adsorbed. The solid of the present invention comprises an inorganic substance and moieties (R10) located on at least one surface of the inorganic substance, wherein said inorganic substance is an inorganic oxide and the surface moiety is selected from the group consisting of -CH2OH, -CH(OH)2, -CH(OH)CH3, -CH2CH2OH, - C(OH)2CH3, -CH2CH(OH)2 and -CH(OH)CH2(OH). Binding moiety, optionally attached to the inorganic substance via a linker, can also be located on the surface of the solid.

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29-01-2009 дата публикации

SEPARATION MATRIX

Номер: CA0002693334A1
Принадлежит:

The present invention relates to a separation matrix, which comprises a support; extenders coupled to an outer part of said support; and ligands coupled to said extenders, wherein the part of the support to which the extenders are coupled constitutes less than 50% of the volume of the separation matrix. The invention also embraces a method of preparing such a separation matrix, as well as a process wherein the separation media is used.

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16-11-2006 дата публикации

AFFINITY ADSORBENTS FOR PLASMINOGEN

Номер: CA0002607851A1
Принадлежит:

For the separation, removal, isolation, purification, characterisation, identification or quantification of plasminogen or a protein that is a plasminogen analogue, an affinity adsorbent is used that is a compound of formula (II) wherein one X is N and the other is N, C-Cl or C-CN; A is a support matrix, optionally linked to the triazine ring by a spacer; Z is O, S or N-R and R is H, C1-6 alkyl, C1-6 hydroxyalkyl, benzyl or .beta.- phenylethyl; B is an optionally substituted hydrocarbon linkage containing from 1 to 10 carbon atoms; D is H, OH or a primary amino, secondary amino, tertiary amino, quaternary ammonium, imidazole, guanidino or amidino group; or B-D is -CHCOOH-(CH2)3-4-NH2; and q is 2 to 6.

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29-11-2011 дата публикации

NOVEL AFFINITY LIGANDS AND THEIR USE

Номер: CA0002232626C

The present invention relates to novel affinity ligand-matrix conjugates comprising a ligand with general formula (a), which ligand is attached to a support matrix in position (A), optionally through a spacer arm interposed between the matrix and ligand. The invention furthermore relates to these novel affinity ligand-matrix conjugates and the preparation and use thereof in the purification of proteinaceous materials such as e.g. immunoglobulins, insulins, Factor VII, or human Growth Hormone or analogues, derivates and fragments thereof and precursors.

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27-03-1997 дата публикации

NOVEL AFFINITY LIGANDS AND THEIR USE

Номер: CA0002232626A1
Принадлежит:

The present invention relates to novel affinity ligand-matrix conjugates comprising a ligand with general formula (a), which ligand is attached to a support matrix in position (A), optionally through a spacer arm interposed between the matrix and ligand. The invention furthermore relates to these novel affinity ligand-matrix conjugates and the preparation and use thereof in the purification of proteinaceous materials such as e.g. immunoglobulins, insulins, Factor VII, or human Growth Hormone or analogues, derivates and fragments thereof and precursors.

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15-02-2018 дата публикации

FILTRATION DEVICE

Номер: WO2018029365A1
Принадлежит:

The invention relates to a filtration device1comprising at least one active layer 2 and at least one antimicrobial composite3. The invention further concerns a method for producing a filtration device and filter systems comprising at least two substrates or components. The filtration device 1 may comprise two substrates, substrate A being provided with a chemically functionalized graphene or graphene oxide layer (active layer 2) and substrate B being coated with an antimicrobial composite 3 comprising silver and ruthenium ("AGXX"). The active layer 2 comprises graphene or graphene oxide functionalized by ionic groups so that it can attract microorganisms 4 and endotoxins (Step I), which are then captured and bound by the active layer 2 (Step II). The antimicrobial composite 3 produces and releases reactive oxygen species ("ROS") which kill microorganisms present in the surroundings (Step III). As the cell structure of the microorganisms is destroyed during the killing process, the cell ...

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16-04-2015 дата публикации

METHOD FOR PRODUCTION OF A CHROMATOGRAPHY MATERIAL

Номер: WO2015053701A1
Автор: SÖDERMAN, Tobias, E.
Принадлежит:

The present invention relates to a method for production of a chromatography material. More closely, the invention relates to a method for production of a reverse phase chromatography (RPC) material comprising the following steps: introduction of unsaturated groups onto porous carbohydrate particles and grafting of styrenic monomers on said particles comprising an unsaturated group..

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01-09-2011 дата публикации

LIGANDS FOR ANTIBODY PURIFICATION BY AFFINITY CHROMATOGRAPHY

Номер: WO2011104307A3
Принадлежит:

The present invention relates to the use, for affinity purification of a protein, of a compound according to the general formula (I), wherein A is selected f The present invention relates to compounds according to the general formula (I), and to their use for affinity purification of a protein. Preferably, the entity to be separated or purified is an antibody, in particular an antibody of the Bevacizumab type or the Ranibizumab type.

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21-02-1984 дата публикации

Organo-mercurial materials

Номер: US0004432877A1
Автор: Tzodikov; Nathan R.
Принадлежит: New England Nuclear Corporation

Compositions in which organo-mercurial moieties are bound to glass or other inorganic substrates are useful in separating sulfhydryl-containing compounds from mixtures with other compounds, e.g., by affinity chromatography.

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31-08-1999 дата публикации

Chromatographic resins and methods for using same

Номер: US0005945520A
Автор:
Принадлежит:

Disclosed are rationally designed mixed mode resins which are useful in recovering a target compound from an aqueous solution and methods for use of such resins. The resins described herein have a hydrophobic character at the pH of binding of the target compound and a hydrophilic and/or electrostatic character at the pH of desorption of the target compound from the resin and are specifically designed to bind the target compound from an aqueous solution at both a low and high ionic strength.

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19-07-2007 дата публикации

Affinity resin

Номер: US2007167594A1
Принадлежит:

A resin which is prepared by polymerizing a monomer component incorporating a hydrophilic spacer, and a ligand-immobilized solid phase carrier obtained by immobilizing a ligand to the resin, are capable of reducing the non-specific adsorption of substances, other than the target molecule for the ligand, which mingle in the sample, to the resin and/or the ligand. Therefore, target molecule search, identification and the like with less noise are enabled.

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23-11-2016 дата публикации

CHROMATOGRAPHIC MATERIAL FOR THE ABSORPTION OF PROTEINS AT PHYSIOLOGICAL IONIC STRENGTH

Номер: EP1715948B1
Принадлежит: PALL CORPORATION

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10-02-1999 дата публикации

СПОСОБ ПОЛУЧЕНИЯ СОРБЕНТА

Номер: RU2125907C1

Использование: в области хроматографии гликопротеинов. Сущность: агарозный гель обрабатывают диглицидиловым эфиром этиленгликоля, м-аминофенилборной кислотой и раствором нитрита натрия. Способ позволяет получить сорбент с высокой емкостью и стабильными свойствами.

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15-12-2017 дата публикации

СОРБЕНТ ДЛЯ ОПРЕДЕЛЕНИЯ СОЕДИНЕНИЙ ИОННОЙ И ГИДРОФИЛЬНОЙ ПРИРОДЫ

Номер: RU2638660C1

Изобретение относится к сепарационным материалам, которые могут быть использованы в ионной хроматографии в качестве сорбентов для определения органических и неорганических анионов, а также в режиме гидрофильной хроматографии для определения полярных биологически активных соединений. Сорбент содержит матрицу на основе силикагеля с привитой четвертичной аммониевой группой и соединённые с ней с помощью спейсеров атомы азота с заместителями, входящие в состав диамина или триамина. Сорбент обладает улучшенными эксплуатационными и хроматографическими характеристиками. Сорбент эффективен для разделения неорганических анионов, слабоудерживаемых органических кислот, аминокислот, сахаров и витаминов. 8 з.п. ф-лы, 1 ил., 1 табл., 11 пр.

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13-02-2014 дата публикации

Separation material comprising saccharide ligands

Номер: AU2012293700A1
Принадлежит:

The present disclosure relates to a separation material comprising a saccharide that is bound via a linker to a matrix for enabling the separation of substances from a liquid that selectively bind to saccharide moieties, to a method for preparing such material, to a method for separating substances from a liquid that selectively bind to saccharides, and to a device comprising a separation material for separating substances from a liquid that selectively bind to saccharides.

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04-02-2016 дата публикации

Affinity chromatography matrix

Номер: AU2014285971A1
Принадлежит:

The invention relates to an affinity chromatography matrix, in the form of a gel, comprising polymer particles onto which at least one oligosaccharide corresponding to a blood group A and/or blood group B epitope is grafted, via a spacer, characterized in that the oligosaccharide density is between 0.2 and 0.7 mg/ml of matrix. The invention also relates to the uses of this matrix for preparing immunoglobulin concentrates for therapeutic use.

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27-09-2012 дата публикации

Activated solid support and method

Номер: US20120245301A1
Принадлежит: GE Healthcare Bio Sciences AB

Disclosed is a method for activating a solid support material with epoxy groups and for immobilising ligands thereon, utilising phase transfer catalytic conditions. The method permits the introduction of epoxy groups and specific nucleophilic ligands on the support material with a high level of substitution. Furthermore, the invention provides a general method for immobilising a ligand for use in a wide variety of chromatographic separation procedures such as ion exchange chromatography, hydrophobic interaction chromatography (HIC), reverse phase chromatography (RPC), or affinity chromatography.

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28-11-2013 дата публикации

ORGANIC-INORGANIC HYBRID CHIRAL SORBENT AND PROCESS FOR THE PREPARATION THEREOF

Номер: US20130317244A1

The present invention provides an organic-inorganic hybrid chiral sorbent for chiral resolution of various racemic compounds viz. racemic mandelic acid, 2-phenyl propionic acid, diethyl tartrate, 2,2′-dihydroxy-1,1′-binaphthalene (BINOL) and cyano chromene oxide with excellent chiral separation (enantiomeric excess, 99%) in case of mandelic acid under medium pressure column chromatography. These optically pure enantiomers find applications as intermediates in pharmaceutical industries. 119.-. (canceled)20. A process for preparation of an organic-inorganic hybrid chiral sorbent comprising an anilino alcohol or a substituted anilino alcohol covalently bonded to a surface of a mesoporous silica material , the process comprising the steps of:(a) silylating a chiral epoxide with a silylating agent in an organic solvent with a molar ratio of the chiral epoxide to the silylating agent of about 1:1 to 1:2.5 in the presence of an inorganic base;(b) refluxing a reaction mixture obtained in the step (a) under an inert atmosphere for a period of 8 to 16 hours, followed by filtration to obtain a resultant filtrate;(c) refluxing the resultant filtrate obtained in the step (b) with the mesoporous silica, under inert atmosphere for a period of about 35 to 55 hours, followed by filtration and washing of a resultant solid product with toluene; and(d) reacting a resultant washed product obtained in the step (c) with aniline or substituted aniline in toluene, under reflux, under inert atmosphere for a period of 8 to 16 hours, followed by filtration and washing off a resultant reaction product with toluene and extracting the organic-inorganic hybrid chiral sorbent.21. The process according to claim 20 , wherein the chiral epoxide in the step (a) is selected from the group consisting of propene oxide claim 20 , 1-chloro-2 claim 20 ,3-epoxypropane claim 20 , 1-fluoro-2 claim 20 ,3-epoxypropane claim 20 , 1-bromo-2 claim 20 ,3-epoxypropane claim 20 , 1-methyl-2 claim 20 ,3-epoxypropane ...

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05-12-2013 дата публикации

POROUS INORGANIC/ORGANIC HYBRID MONOLITH MATERIALS FOR CHROMATOGRAPHIC SEPARATIONS AND PROCESS FOR THEIR PREPARATION

Номер: US20130324395A1
Принадлежит: WATERS TECHNOLOGIES CORPORATION

Novel materials for chromatographic separations, processes for their preparation, and separation devices containing the chromatographic materials. In particular, the novel materials are porous inorganic/organic hybrid monolith materials, which desirably may be surface modified, and which offer more efficient chromatographic separations than that known in the art. 1134-. (canceled)135. A method of preparation of a porous inorganic/organic hybrid monolith material , comprising coalesced porous particles of hybrid silica having a chromatography-enhancing pore geometry , comprising the steps ofa) prepolymerizing a mixture of one or more organoalkoxysilanes and a tetraalkoxysilane in the presence of an acid catalyst to produce a polyorganoalkoxysiloxane;b) preparing an aqueous suspension of said polyorganoalkoxysiloxane, said suspension further comprising a surfactant or combination of surfactants, and gelling in the presence of a base catalyst so as to produce porous hybrid particles;c) modifying the pore structure of said porous hybrid particles by hydrothermal treatment; andd) coalescing said porous hybrid particles to form a monolith material thereby preparing a porous inorganic/organic hybrid monolith material.136152-. (canceled)153. A porous inorganic/organic hybrid monolith material comprising coalesced porous hybrid particles of hybrid silica having a chromatographically-enhancing pore geometry , produced by the process ofa) prepolymerizing a mixture of one or more organoalkoxysilanes and a tetraalkoxysilane in the presence of an acid catalyst to produce a polyorganoalkoxysiloxane;b) preparing an aqueous suspension of said polyorganoalkoxysiloxane, said suspension further comprising a surfactant or a combination of surfactants, and gelling in the presence of a base catalyst so as to produce porous hybrid particles;c) modifying the pore structure of said porous hybrid particles by hydrothermal treatment; andcoalescing said porous hybrid particles to form a ...

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05-12-2013 дата публикации

ZWITTERIONIC STATIONARY PHASE FOR HYDROPHILIC INTERACTION LIQUID CHROMATOGRAPHY AND PREPARATION METHOD THEREOF

Номер: US20130324700A1

A type of liquid chromatographic stationary phase and preparation method thereof, the bonding terminal of the chromatographic stationary phase is zwitterionic functional group. The preparation method includes the following steps, alkenyl or alkynyl silane is bonded onto the surface of silica based on the horizontal polymerization approach to obtain alkenyl- or alkynyl-modified silica. Then the thiol click reaction with zwitterionic compound containing thiol group is performed to obtain the zwitterionic hydrophilic interaction chromatographic stationary phase. The present stationary phase possesses both zwitterionic characteristics and excellent hydrophilicity. It can be widely applied in the separation of variety of samples. 2. A preparation method for the stationary phases as described in claim 1 , characterized in that:a. Pretreatment of silica: after adding hydrochloric acid or nitric acid aqueous solution with the concentration of 1˜38 wt % into silica gel, the solution is heated to reflux while stirring for 1˜48 hours. The resulted material is filtered, washed with water until neutral and dried to constant weight under 100˜160° C. After that, the dried silica gel is placed in nitrogen or argon atmosphere with the humidity of 20˜80% for 24˜72 hours until the weight increment is 0.5˜10 wt % to obtain the humidified silica.b. Polymerization on silica surface: the humidified silica obtained from step a is first placed in reaction vessel made of glass or polytetrafluoroethylene, and organic solvent is added under nitrogen atmosphere. The solution is stirred and mixed well, and then alkenyl or alkynyl silane is dropwise added. The reaction is performed under 20˜200° C. for 2˜48 hours with continuous stirring. After that, the reaction is cooled to room temperature. The reaction product is filtered and washed by toluene, dichloromethane, methanol, water, tetrahydrofuran and methanol successively. The solid product is dried under 60˜100° C. for 12˜24 hours to obtain ...

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07-01-2016 дата публикации

INTEGRATED HIGH THROUGHPUT SYSTEM FOR THE ANALYSIS OF BIOMOLECULES

Номер: US20160003841A1
Принадлежит:

Described is an affinity microcolumn comprising a high surface area material, which has high flow properties and a low dead volume, contained within a housing and having affinity reagents bound to the surface of the high surface area material that are either activated or activatable. The affinity reagents bound to the surface of the affinity microcolumn further comprise affinity receptors for the integration into high throughput analysis of biomolecules. 1. An affinity microcolumn comprising a polymer contained within a housing and affinity reagents bound to the polymer , wherein the affinity reagents are either activated or activatable.2. The affinity microcolumn of wherein the polymer is formed by molding.3. The affinity microcolumn of wherein the polymer is exposed to at least one of chemical etching and electro etching.4. The affinity microcolumn of wherein the affinity reagents that are bound to the polymer further comprise affinity receptors bound to the affinity reagents.5. The affinity microcolumn of further comprising a tethering molecule that is activated or activatable and binds the affinity receptors to the affinity reagents.6. The affinity microcolumn of further comprising an amplification media that is activated or activatable and is interposed between the affinity reagents and the affinity receptors claim 4 , where the amplification media allows a high density of affinity receptors to be bound to the affinity reagents than in the absence of the amplification media.7. The affinity microcolumn of further comprising an amplification media interposed between the affinity reagents and the affinity receptors claim 4 , where the amplification media allows better access by an analyte to the affinity receptors than in the absence of the amplification media.8. The affinity microcolumn of wherein the amplification media comprises at least one of a biological polymer claim 6 , a non-biological organic polymer claim 6 , and an inorganic polymer.9. The affinity ...

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27-01-2022 дата публикации

SOLID-PHASE CHELATOR MATERIAL, METHOD FOR PRODUCING THEREOF AND USE THEREOF FOR THE PURIFICATION OF PROTEINS

Номер: US20220023851A1
Автор: Fabis Roland
Принадлежит:

A solid-phase chelator material usable for the purification of proteins. The solid-phase chelator material comprises a solid phase, polyamine groups bound to the solid phase and chelating groups bound to the polyamine groups. At least a part of the polyamine groups is connected with at least two chelating groups per polyamine group. Each chelating group comprises one or several aminopolycarboxylic acid groups (APA groups), with the proviso that the number of APA groups per polyamine group connected with at least two cheating groups is at least three. 1. A solid-phase chelator material comprising a solid phase , polyamine groups bound to the solid phase and chelating groups bound to the polyamine groups , wherein at least a part of the polyamine groups are connected with at least two chelating groups per polyamine group and wherein each chelating group comprises one or several aminopolycarboxylic acid groups (APA groups) , with the proviso that the number of APA groups per polyamine group connected with at least two chelating groups is at least three.2. The solid-phase chelator material according to claim 1 , wherein the chelating groups are selected from the group consisting of individual APA groups claim 1 , linear chelator chains formed by two or more APA groups which are connected with each other via bifunctional linker moieties K claim 1 , branched chelator chains formed by three or more APA groups connected with each other via trifunctional linker moieties L claim 1 , and mixed chelator chains formed by four or more APA groups connected with each other via at least one bifunctional linker moiety K and at least one trifunctional linker moiety L.3. The solid-phase chelator material according to claim 1 , wherein the number of chelating groups bound to a polyamine group is at least three claim 1 , preferably at least four claim 1 , and/or wherein the number of APAs which is coupled to a polyamine group connected with at least two chelating groups is in the range ...

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03-02-2022 дата публикации

MATERIALS FOR HYDROPHILIC INTERACTION CHROMATOGRAPHY AND PROCESSES FOR PREPARATION AND USE THEREOF FOR ANALYSIS OF GLYCOPROTEINS AND GLYCOPEPTIDES

Номер: US20220034852A1
Принадлежит:

The invention relates to poly-amide bonded hydrophilic interaction chromatography (HILIC) stationary phases and novel HILIC methods for use in the characterization of large biological molecules modified with polar groups, known to those skilled in the art as glycans. The invention particularly provides novel, poly-amide bonded materials designed for efficient separation of large biomolecules, e.g. materials having a large percentage of larger pores (i.e. wide pores). Furthermore, the invention advantageously provides novel HILIC methods that can be used in combination with the stationary phase materials described herein to effectively separate protein and peptide glycoforms by eliminating previously unsolved problems, such as on-column aggregation of protein samples, low sensitivity of chromatographic detection of the glycan moieties, and low resolution of peaks due to restricted pore diffusion and long intra/inter-particle diffusion distances. 149-. (canceled)50. A method for analyzing a glycosylated proteinaceous sample , comprising contacting the sample with a chromatographic material in the presence of a mobile phase eluent to thereby analyze the sample , wherein the chromatographic material is a porous material which comprises at least one hydrophilic monomer and a poly-amide bonded phase.51. The method of claim 50 , wherein an average pore diameter of the porous material is greater than or equal to about 200 Å.52. The method of claim 50 , wherein an average pore diameter of the porous material is ranges from about 200 Å to about 450 Å.53. The method of claim 50 , wherein the porous material has an average pore diameter of about 300 Å.54. The method of claim 50 , wherein the mobile phase eluent is a high organic eluent.55. The method of claim 50 , wherein the mobile phase eluent comprises acetonitrile claim 50 , isopropanol claim 50 , n-propanol claim 50 , methanol claim 50 , ethanol claim 50 , butanol claim 50 , water claim 50 , or a mixture thereof.56. The ...

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17-01-2019 дата публикации

PACKING MATERIAL FOR LIQUID CHROMATOGRAPHY AND COLUMN FOR LIQUID CHROMATOGRAPHY

Номер: US20190015813A1
Принадлежит: SHOWA DENKO K.K.

A packing material for liquid chromatography, which is excellent in durability, and a column for liquid chromatography, which is filled with the packing material, are provided. The packing material for liquid chromatography is characterized by comprising a hydrophilic resin containing a polyvinyl alcohol resin, to said hydrophilic resin an amino group represented by the formula (1) having been bonded through a spacer. In the formula (1), Rrepresents a hydrogen atom or an alkyl group having 1 to 4 carbon atoms, Rrepresents an alkyl group having 1 to 6 carbon atoms and having one or more hydroxyl groups, and ※ represents a bonding position to the spacer. 2. The packing material for liquid chromatography as claimed in claim 1 , wherein Ris a hydrogen atom or a methyl group.4. The packing material for liquid chromatography as claimed in claim 1 , wherein the amino group represented by the formula (1) is derived from any one amine of the group consisting of D-glucamine claim 1 , N-methyl-D-glucamine claim 1 , 1-amino-1-deoxy-D-mannitol claim 1 , 1-amino-1-deoxy-D-galactitol claim 1 , 1-amino-1-deoxy-D-iditol claim 1 , 1-amino-1-deoxy-D-arabinitol claim 1 , 1-amino-1-deoxy-D-xylitol claim 1 , 4-amino-1 claim 1 ,2 claim 1 ,3-butanetriol claim 1 , 3-amino-1 claim 1 ,2-propanediol and 3-methylamino-1 claim 1 ,2-propanediol.5. The packing material for liquid chromatography as claimed in claim 1 , wherein the spacer is derived from a compound having a glycidyl group at an end.6. A column for liquid chromatography claim 1 , using the packing material for liquid chromatography as claimed in . This is a divisional of U.S. application Ser. No. 15/121,806 filed Aug. 26, 2016, which is a National Stage of International Application No. PCT/JP2015/055031, filed Feb. 23, 2015, claiming priority based on Japanese Patent Application No. 2014-038331, filed Feb. 28, 2014, the contents of all of which are incorporated herein by reference in their entirety.The present invention relates to a ...

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15-01-2015 дата публикации

Fc-receptor based affinity chromatography

Номер: US20150018241A1
Принадлежит: Hoffmann La Roche Inc

Herein is reported the use of an immobilized non-covalent complex of a neonatal Fc receptor (FcRn) and beta-2-microglobulin (b2m) as affinity chromatography ligand in general and, for example, for the determination of the in vivo half-live of an antibody by determining the ratio of the retention times of the antibody and a reference antibody.

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28-01-2016 дата публикации

IODINE ADSORBENT, WATER TREATMENT TANK AND IODINE ADSORBING SYSTEM

Номер: US20160023923A1
Принадлежит: KABUSHIKI KAISHA TOSHIBA

An iodine adsorbent of an embodiment has a support, a first organic group bonded to the support and has a functional group containing nitrogen at least at a terminal, and silver bonded to the nitrogen-containing functional group. 1. An iodine adsorbent comprising:a support;a first organic group bonded to the support and has a functional group containing nitrogen at least at a terminal; andsilver bonded to the nitrogen-containing functional group.2. The adsorbent according to claim 1 , wherein the nitrogen-containing functional group is a functional group having an amine or an amine derivative structure.3. The adsorbent according to claim 1 , wherein the nitrogen-containing functional group includes at least one of an amino group claim 1 , an amide group claim 1 , and a guanidino group.4. The adsorbent according to claim 1 , further comprising a second organic group bonded to the support and has a functional group containing sulfur at least at a terminal claim 1 , and the sulfur-containing functional group includes at least one of a thiol group claim 1 , a thiolate group claim 1 , a sulfide group claim 1 , and a disulfide group.5. The adsorbent according to claim 4 , wherein an atomic concentration ratio (S (atm %)/N (atm %)) of sulfur to nitrogen in the adsorbent is less than 2.0.6. The adsorbent according to claim 1 , wherein the first organic group contains a carbon chain claim 1 , and a concentration of carbon atoms in the adsorbent is 50 (atm %) or less.7. The adsorbent according to claim 4 , wherein the first organic group contains a carbon chain claim 4 , the second organic group contains a carbon chain claim 4 , and a concentration of carbon atoms in the adsorbent is 50 (atm %) or less.8. A water treatment tank comprising an iodine adsorbent stored therein claim 4 , whereinthe iodine adsorbent includes a support,a first organic group bonded to the support and has a functional group containing nitrogen at least at a terminal, andsilver bonded to the nitrogen- ...

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24-01-2019 дата публикации

Multimodal Anion Exchange Matrices

Номер: US20190023735A1
Принадлежит: GE Healthcare BioProcess R&D AB

The invention discloses a separation matrix which comprises a plurality of separation ligands, defined by the formula R 1 -L 1 -N(R 3 )-L 2 -R, immobilized on a support, wherein R 1 is a five- or six-membered, substituted or non-substituted ring structure or a hydroxyethyl or hydroxypropyl group; L 1 is either a methylene group or a covalent bond; R 2 is a five-or six-membered, substituted or non-substituted ring structure; L 2 is either a methylene group or a covalent bond; R 3 is a methyl group; and wherein if R 1 is a hydroxyethyl group and L 1 is a covalent bond, R 2 is a substituted aromatic ring structure or a substituted or non-substituted aliphatic ring structure.

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23-01-2020 дата публикации

Novel Chromatography Media

Номер: US20200023338A1
Принадлежит: GE Healthcare BioProcess R&D AB

The present invention relates to a novel chromatography media, more closely a novel IMAC (Immobilized Metal Affinity Chromatography) media. The novel chromatography media comprises a pentaligand and provides high dynamic binding capacity as well as high purity of the sample proteins purified on the media of the invention. 1. An immobilized metal affinity chromatography (IMAC) medium , comprising a pentadentate ligand coupled to a 5-60 μm diameter chromatography bead Q.3. The medium according to claim 2 , wherein the QB10% is at least 3 times more.4. The medium according to claim 1 , wherein Q is a porous natural or synthetic polymer claim 1 , preferably agarose.5. The medium according to claim 1 , wherein Q is made of agarose and the diameter of Q is 30-40 μm.6. The medium according to claim 1 , wherein Q is dextran coated.7. The medium according to claim 2 , wherein n is 2 claim 2 , i.e. ethylene and S should preferably be a hydrophilic chain of C and O comprising at least 3 atoms.8. The medium according to claim 2 , wherein the Q adsorbent is charged with metal ions selected from the group that consists of Cu2+ claim 2 , Ni2+ claim 2 , Zn2+ claim 2 , Co2+ claim 2 , Fe3+ and Ga3+.9. The method according to claim 1 , wherein Q comprises magnetic particles.10. A method for purification of a biomolecule on an IMAC medium comprising loading a sample on a medium according to one or more of the above claims claim 1 , wherein the sample comprises chelating agents claim 1 , such as EDTA claim 1 , and the dynamic binding capacity at QB10% is more than double compared to conventional IMAC media.11. The method according to claim 10 , wherein the IMAC medium is a pentadentate medium of and QB10% is 3 to 6 times higher.12. The method according to claim 10 , wherein the biomolecule is labelled with at least two claim 10 , preferably at least six claim 10 , His-residues.13. An IMAC medium comprising a tetra or pentadentate ligand coupled to a chromatography bead made of agarose ...

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28-01-2021 дата публикации

CHROMATOGRAPHIC MATERIALS FOR THE SEPARATION OF UNSATURATED MOLECULES

Номер: US20210023531A1
Принадлежит: WATERS TECHNOLOGIES CORPORATION

The present disclosure relates to a method of separating a compound of interest, particularly unsaturated compound(s) of interest, from a mixture. The compound is separated using a column having a chromatographic stationary phase material for various different modes of chromatography containing a first substituent and a second substituent. The first substituent minimizes compound retention variation over time under chromatographic conditions. The second substituent chromatographically and selectively retains the compound by incorporating one or more aromatic, polyaromatic, heterocyclic aromatic, or polyheterocyclic aromatic hydrocarbon groups, each group being optionally substituted with an aliphatic group. In some examples, the present disclosure can include a chromatographic system having a chromatographic column having a stationary phase with a chromatographic substrate containing silica, metal oxide, an inorganic-organic hybrid material, a group of block copolymers, or a combination thereof. 2. The stationary phase of claim 1 , wherein the surface of X is subject to alkoxylation by a chromatographic mobile phase under chromatographic conditions.3. The stationary phase of claim 2 , wherein a substantial portion of the surface of X does not undergo alkoxylation by a chromatographic mobile phase under chromatographic conditions.4. The stationary phase of claim 1 , wherein the surface of X does not comprise silica claim 1 , and b=0 or c=0.5. The stationary phase of claim 1 , wherein the chromatographic stationary phase is adapted for supercritical fluid chromatography.6. The stationary phase of claim 1 , wherein the chromatographic stationary phase is adapted for carbon dioxide based chromatography.7. A column claim 1 , capillary column claim 1 , microfluidic device or apparatus for normal phase chromatography claim 1 , high-pressure liquid chromatography claim 1 , solvated gas chromatography claim 1 , supercritical fluid chromatography claim 1 , sub-critical fluid ...

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29-01-2015 дата публикации

APPLICATION OF MACROPOROUS SILICA SYNTHESIZED BY A SALT-TEMPLATED AEROSOL METHOD FOR CHROMATOGRAPHY

Номер: US20150027953A1
Принадлежит:

The present invention discloses a silica particle having a diameter less than or equal to 2 μη, wherein the particle is spherical and comprises interconnected pores having a diameter in the range from 50 nm to 300 nm. The silica particle is preferably produced by spray pyrolysis (=spray drying) of a silica colloid. In the production process, porosity is introduced by means of an inorganic salt, such as NaCl, KCI, LiCl, NaNO3 or Ll NO3, which serves as a pore template. The silica particle may further be functionalized with proteins, peptides, nucleic acids, polysaccharides and proteoglycans, preferably concanavalin A or avidin. The present invention further discloses the use of the silica particle in chromatography, in particular in affinity chromatography. 1. A silica particle having a diameter less than or equal to about 2 μm , wherein the particle is spherical and comprises interconnected pores having a diameter in the range from about 50 nm to about 300 nm.2. The silica particle of claim 1 , wherein the silica particle provides a support with a surface area of about 150 m/g to about 300 m/g.3. The silica particle of claim 1 , wherein the silica particle is functionalized with a stationary phase.4. The silica particle of claim 3 , wherein the stationary phase is selected from the group consisting of proteins claim 3 , peptides claim 3 , nucleic acids claim 3 , polysaccharides claim 3 , and proteoglycans.5. The silica particle of claim 4 , wherein the proteins are concanavalin A or avidin.6. The silica particle of claim 1 , wherein the silica particle is synthesized by spray pyrolysis of silica colloids.7. The silica particle of claim 6 , wherein porosity is introduced into the particle by means of an inorganic salt acting as a pore template.8. The silica particle of claim 7 , wherein the inorganic salt is selected from the group consisting of NaCl claim 7 , KCl claim 7 , LiCl claim 7 , NaNO claim 7 , LiNO claim 7 , combinations thereof claim 7 , and mixtures ...

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17-02-2022 дата публикации

Ligand linker substrate

Номер: US20220048010A1
Принадлежит:

Ligand functionalized substrate including a solid substrate, which has been modified to provide grafted catching ligand groups covalently bound via a linker, methods of preparing the ligand functionalized substrate and the use thereof, such as to increase binding rate and the dynamic binding capacity (DBC). 1. A ligand-functionalized substrate comprising:{'sub': '2', '#text': 'a. a substrate having carboxylic (—COOH), hydroxy (—OH), thio (—SH), amino groups (—NH), C═C double bonds (-ene) or C—C triple bonds (-yne) at the surface thereof;'}b. covalently bound to said carboxylic (—COOH), hydroxy (—OH), thio (—SH), amino groups (—NH2), C═C double bonds (-ene) or C—C triple bonds (-yne) of said substrate a linker having a linker length of 10-25, such as 17-22 bonds, wherein bonds are C—C, C—N, C—N(H), C—C(O) and/or C—O; andc. a ligand-functional group bound to the surface of the substrate via said linker.2. The ligand-functionalized substrate according to claim 1 , wherein the substrate is a solid substrate.3. The ligand-functionalized substrate according to claim 1 , wherein the substrate is a solid substrate which can be grafted by radical initiated vinyl polymerization.4. The ligand-functionalized substrate according to claim 1 , wherein the substrate is selected from the group consisting of agarose claim 1 , such as in the form of a resin or beads claim 1 , kieselguhr claim 1 , silica gel claim 1 , cellulose claim 1 , cellulose ethers claim 1 , carboxymethyl cellulose claim 1 , degenerated cellulose claim 1 , agarose or paper based membranes claim 1 , nitrocellulose claim 1 , nitrocellulose mixed esters claim 1 , silicas claim 1 , and controlled pore glasses claim 1 , polyamides claim 1 , poly sulfone ether claim 1 , polyvinylalcohols claim 1 , polycarbonate claim 1 , polyurethane claim 1 , polyethersulfone claim 1 , polysulfone claim 1 , polyethylene terephthalate claim 1 , polyvinylidene fluoride claim 1 , polystyrene or polypropylene claim 1 , polyethylene and co ...

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09-02-2017 дата публикации

SUPERHYDROPHOBIC SPONGE AS AN EFFICIENT OIL ABSORBENT MATERIAL FOR OIL SPILL CLEANUP APPLICATIONS

Номер: US20170036190A1
Принадлежит: Brookhaven Science Associates, LLC

This disclosure describes hydrophobic or super-hydrophobic compositions, such as sponges, that also are oleophilic or super-oleophilic with superior recyclability, good mechanical strength, low cost, and manufacture scalability. The hydrophobic or super-hydrophobic compositions include the reaction product of at least a substrate having a reacting group which reacts with a silane and an alkylsilane or a fluoroalkylsilane having an alkyl group comprised of a hydrocarbon, an aliphatic hydrocarbon, or a fluorohydrocarbon of 1 to about 30 carbon atoms. 1. A hydrophobic composition , comprising the reaction product of at least:a substrate having a reacting group which reacts with a silane; andan alkylsilane having an alkyl group comprised of a hydrocarbon, an aliphatic hydrocarbon, or a fluorohydrocarbon of 1 to about 30 carbon atoms.2. The hydrophobic composition of claim 1 , wherein the alkylsilane has a structure R—Si—(CH)(Z) claim 1 , where R is the alkyl group comprised of a hydrocarbon claim 1 , an aliphatic hydrocarbon claim 1 , or a fluorohydrocarbon of 1 to about 30 carbon atoms claim 1 , Z is selected from at least one of Br claim 1 , Cl claim 1 , F claim 1 , an alkoxy group having from 1 to 3 carbon atoms or chlorine atoms claim 1 , or a combination thereof claim 1 , x is 1 or 2 claim 1 , and y is 0 claim 1 , 1 claim 1 , or 2.3. The hydrophobic composition of claim 2 , wherein the alkylsilane is an alkyltrichlorosilane claim 2 ,4. The hydrophobic composition of claim 3 , wherein the alkyl group comprises a hydrocarbon claim 3 , an aliphatic hydrocarbon claim 3 , or a fluorohydrocarbon of from about 12 to about 20 carbons.5. The hydrophobic composition of claim 1 , wherein the alkylsilane comprises at least one of octadecyltrichlorosilane claim 1 , dodecyltrichlorosilane claim 1 , octyltrichlorosilane claim 1 , butyltrichlorosilane.6. The hydrophobic composition of claim 1 , wherein the substrate comprises an open cell foam or a fabric.7. The hydrophobic ...

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24-02-2022 дата публикации

MULTIMODAL ADSORPTION MEDIUM WITH MULTIMODAL LIGANDS, METHOD FOR THE PREPARATION AND USE THEREOF

Номер: US20220055015A1
Принадлежит: SARTORIUS STEDIM BIOTECH GMBH

The present invention relates to a multimodal adsorption medium, in particular a multimodal chromatography medium, a method for its production, as well as use of the adsorption medium according to the invention or an adsorption medium produced according to the invention for the purification of biomolecules. 2. The multimodal adsorption medium as claimed in claim 1 , wherein the polymeric carrier material comprises at least one material selected from the group composed of natural or synthetic fibers claim 1 , (polymer) membranes claim 1 , porous claim 1 , polymeric monolithic molded bodies claim 1 , polymer gels claim 1 , films claim 1 , nonwovens and wovens.3. The multimodal adsorption medium as claimed in claim 1 , wherein the polymeric spacer elements are polyamines with at least one primary amino group claim 1 , which as an X—(C═O) bond forms an amide bond with the multimodal ligands.4. The multimodal adsorption medium as claimed in claim 3 , wherein the polymeric spacer elements are selected from the group consisting of polyallylamine claim 3 , polyvinylamine claim 3 , polyethyleneimine (branched or linear) claim 3 , poly(4-aminostyrene) claim 3 , chitosan claim 3 , poly-L-lysine claim 3 , poly(N-methylvinylamine) claim 3 , poly(N-methylallylamine) and poly(oleylamine).5. The multimodal adsorption medium as claimed in claim 3 , wherein the polyamine has a molar mass of more than 500 g/mol.6. The multimodal adsorption medium as claimed in claim 4 , wherein the polymeric spacer elements are selected from the group of polyallylamines with a molar mass of 3 claim 4 ,000 to 150 claim 4 ,000 g/mol.7. The multimodal adsorption medium as claimed in claim 1 , wherein the ligand density of the multimodal ligands of the adsorption medium is at least 25 μmol/ml.8. A method for producing an adsorption medium as claimed in claim 1 , comprising the following steps:(a) providing a polymeric carrier material with polymeric spacer elements bound to the surface thereof, wherein ...

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12-02-2015 дата публикации

SORBENT COMPRISING ON ITS SURFACE AN AROMATIC RING SYSTEM HAVING AN ANIONIC OR DEPROTONIZABLE GROUP FOR THE PURIFICATION OF ORGANIC MOLECULES

Номер: US20150045545A1
Принадлежит:

The present invention relates to a sorbent comprising a solid support material, the surface of which comprises a residue of a general formula (I), wherein the residue is attached via a covalent single bond to a functional group on the surface of either the bulk solid support material itself or of a polymer film on the surface of the solid support material. Furthermore, the present invention relates to the use of the sorbent according to the invention for the purification of organic molecules, in particular pharmaceutically active compounds, preferably in chromatographic applications. 114-. (canceled)16. The sorbent of claim 15 , wherein L binds to the functional group via a —C(O)-moiety.17. The sorbent of claim 15 , wherein Ar is a (p+1)-valent mono- or polycyclic aromatic ring system comprising 6 to 20 aromatic ring atoms.19. the sorbent of claim 15 , wherein Pis selected from the group consisting of —OH claim 15 , —COOH claim 15 , —SOH and —B(OH).20. The sorbent of claim 15 , wherein q is 1.21. The sorbent of claim 15 , wherein p is 1 or 3.23. The sorbent of claim 15 , wherein the surface of the solid support material is covered with a film of a polymer comprising individual chains which are covalently crosslinked with each other claim 15 , and wherein the individual chains are not covalently bound to the surface of the solid support material.24. The sorbent of claim 23 , wherein the polymer is a polyamine claim 23 , a polyvinylamine claim 23 , a copolymer comprising polyamine or a polymer blend comprising polyamine.25. A method for the purification of organic molecules claim 15 , comprising contacting organic molecules with the sorbent of .26. The method of claim 25 , wherein the organic molecules are pharmaceutically active compounds.27. The method of claim 25 , wherein the organic molecules exhibit a molecular weight in the range of from 300 to 200000 g/mol.28. the method of claim 25 , wherein the organic molecules are selected from the group consisting of ...

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18-02-2021 дата публикации

CHROMATOGRAPHIC COMPOSITIONS

Номер: US20210046450A1
Принадлежит: WATERS TECHNOLOGIES CORPORATION

Provided herein are stationary phase compositions comprising a chromatographic surface of porous or non-porous core material comprising a surface modifier for use in chromatographic separations. 5. The stationary phase composition of claim 4 , wherein Ris trimethylsilyl.11. The stationary phase composition of claim 10 , wherein Ris trimethylsilyl.12. The stationary phase composition of claim 1 , wherein each b is 0 to 3.13. The stationary phase composition of claim 1 , wherein each b is 0.14. The stationary phase composition of claim 1 , wherein each a is 0 to 3.15. The stationary phase composition of claim 1 , wherein each a is 0.16. The stationary phase composition of claim 1 , wherein each x is 0 to 4.17. The stationary phase composition of claim 1 , wherein each x is 0.18. The stationary phase composition of claim 1 , wherein each y is 0 to 4.19. The stationary phase composition of claim 1 , wherein each y is 0.20. The stationary phase composition of claim 1 , wherein each Rand Rare independently aryl or (C-C)alkyl optionally substituted with cyano. This application is a continuation of U.S. application Ser. No. 15/921,811 entitled “Chromatographic Compositions” filed Mar. 15, 2018, which claims benefit of and priority to U.S. Provisional Application Nos. 62/472,342 entitled “Chromatographic Compositions” filed Mar. 16, 2017, and 62/543,654 entitled “Chromatographic Compositions” filed Aug. 10, 2017, the contents of each of which are incorporated herein by reference in their entirety.The technology relates generally to chromatographic compositions. The invention relates more particularly, in various embodiments, to stationary phase compositions comprising a chromatographic surface of porous or non-porous core material comprising a surface modifier for use in chromatographic separations.Liquid chromatography (LC) combined with mass spectrometry (MS) is one of the most powerful analytical tools for the characterization of proteins. Indeed, for the analysis of ...

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18-02-2021 дата публикации

NOVEL AFFINITY CHROMATOGRAPHY MEDIA FOR REMOVAL OF ANTI-A AND/OR ANTI-B ANTIBODIES

Номер: US20210047430A1
Принадлежит:

Embodiments described herein relate to novel chromatography media for removing anti-A and/or anti-B antibodies from a sample, as well as methods of using the same. The media described herein have several advantages over previously described media including, acid and alkaline stability. 1. A method of removing anti-A antibodies from a sample , the method comprising the steps of:(a) providing a sample comprising an amount of anti-A antibodies;(b) incubating the sample with a media comprising a solid support with a blood group A antigen ligand attached thereto, wherein the ligand is attached to the solid support at a ligand loading of at least 0.8 mg/ml of solid support, and wherein the media is stable under acid and/or alkaline conditions and wherein the solid support comprises a polymer selected from the group consisting of polyvinylether, polyvinylalcohol, polymethacrylate, polyacrylate, polystyrene, polyacrylamide, polymethacrylamide and polycarbonate and the blood group A antigen ligands are attached via pAA tentacle chemistry to a solid support, for the media to bind anti-A antibodies;(c) recovering portion of the sample which is not bound to the media; and(d) measuring amount of anti-A antibodies in the portion of the sample in (c), wherein the amount of anti-A antibodies in (d) is at least 80% less than the amount of anti-A antibodies in the sample in (a).2. A method of removing anti-B antibodies from a sample , the method comprising the steps of:(a) providing a sample comprising an amount of anti-B antibodies;(b) incubating the sample with a media for removing anti-B antibodies from a sample, the media comprising a solid support with a blood group B antigen ligand attached thereto, wherein the ligand is attached to the solid support at a ligand loading of at least 0.8 mg/ml of solid support, and wherein the media is stable under acid and/or alkaline conditions and wherein the solid support comprises a polymer selected from the group consisting of ...

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16-02-2017 дата публикации

Solid-phase carrier, production method for solid-phase carrier, carrier for affinity refining, production method for filler for affinity chromatography, filler for affinity chromatography, chromatography column, and refining method

Номер: US20170043320A1
Принадлежит: JSR Corp, JSR Life Sciences Corp

There are provided a solid-phase carrier and a carrier for affinity refining that exhibit high dynamic binding capacity when a ligand is immobilized, have excellent antifouling properties, and are unlikely to have non-specific adsorption of impurities. The solid-phase carrier has a functional group capable of fixing a ligand and is characterized by having a group having a sulfinyl group, a sulfide group, an oxy group or an imino group, and a hydroxyl group, a thiol group, an amino group, a carboxy group, a sulfate group, a phosphate group or an alkanoyl group.

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15-02-2018 дата публикации

Porous Adsorbent Structure for Adsorption of CO2 from a Gas Mixture

Номер: US20180043303A1

A porous adsorbent structure that is capable of a reversible adsorption and desorption cycle for capturing COfrom a gas mixture comprises a support matrix formed by a web of surface modified cellulose nanofibers. The support matrix has a porosity of at least 20%. The surface modified cellulose nanofibers consist of cellulose nanofibers having a diameter of about 4 nm to about 1000 nm and a length of 100 nm to 1 mm that are covered with a coupling agent being covalently bound to the surface thereof. The coupling agent comprises at least one monoalkyldialkoxyaminosilane. 115-. (canceled)16. A method for producing a porous adsorbent structure that is capable of a reversible adsorption and desorption cycle for capturing COfrom a gas mixture , said structure comprising a support matrix of surface modified cellulose nanofibers , said surface modified cellulose nanofibers consisting of cellulose nanofibers having a diameter of about 4 nm to about 1000 nm and a length of 100 nm to 1 mm covered with a coupling agent being covalently bound to the surface thereof , characterized in that:i) said support matrix is a web of nanofibers with a porosity of at least 20%, and a) providing a first amount of a homogenized suspension of cellulose nanofibers having a diameter of about 4 nm to about 1000 nm and a length of 1.00 nm to 1 mm in a solvent;', 'b) adding thereto a second amount of a coupling agent comprising at least one monoalkyldialkoxyaminosilane, thereby allowing formation of a homogeneous suspension of surface modified cellulose nanofibers in said solvent;', 'c) mechanically concentrating said suspension through centrifugation, filtration or pressing, thereby obtaining a wet slurry;', 'd) optionally washing said wet slurry with said solvent;', 'e) removing said solvent by a drying operation, said drying operation being selected from freeze drying, atmospheric freeze drying, or a combination thereof, thereby obtaining a dried material; and', 'f) subjecting said dried ...

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25-02-2021 дата публикации

POROUS CYCLODEXTRIN POLYMERIC MATERIALS AND METHODS OF MAKING AND USING SAME

Номер: US20210053025A1
Принадлежит:

A nucleophilic substitution reaction to crosslink cyclodextrin (CD) polymer with rigid aromatic groups, providing a high surface area, mesoporous CD-containing polymers (P-CDPs). The P-CDPs can be used for removing organic contaminants from water. By encapsulating pollutants to form well-defined host-guest complexes with complementary selectivities to activated carbon (AC) sorbents. The P-CDPs can rapidly sequester pharmaceuticals, pesticides, and other organic micropollutants, achieving equilibrium binding capacity in seconds with adsorption rate constants 15-200 times greater than ACs and nonporous CD sorbents. The CD polymer can be regenerated several times, through a room temperature washing procedure, with no loss in performance. 5. The mesoporous polymeric material of claim 2 , wherein the molar ratio of cyclodextrin moieties to aryl moieties ranges from about 1:1 to about 1:X claim 2 , wherein X is three times the average number of glucose subunits in the cyclodextrin moieties.6. The mesoporous polymeric material of claim 2 , wherein the cyclodextrin is selected from the group consisting of α- claim 2 , β- claim 2 , γ-cyclodextrin claim 2 , and combinations thereof.7. The mesoporous polymeric material of claim 2 , wherein the cyclodextrin moieties comprise β-cyclodextrin.8. The mesoporous polymeric material of claim 7 , wherein the cyclodextrin moieties comprise β-cyclodextrin and the ratio of β-cyclodextrin moieties to crosslinking moieties is 1:1 to 1:21.9. The mesoporous polymeric material of claim 2 , wherein the mesoporous polymeric material has a Brunauer-Emmett-Teller (BET) surface area of 50 m/g to 2000 m/g.10. The mesoporous polymeric material of claim 3 , wherein the molar ratio of cyclodextrin moieties to aryl moieties ranges from about 1:1 to about 1:X claim 3 , wherein X is three times the average number of glucose subunits in the cyclodextrin moieties.11. The mesoporous polymeric material of claim 3 , wherein the cyclodextrin is selected from ...

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14-02-2019 дата публикации

NANOMETER SIZE CHEMICAL MODIFIED MATERIALS AND USES

Номер: US20190049352A1
Принадлежит:

Ligand compositions and stationary phases comprising polyhedral oligomeric silsesquioxane moieties are incorporated in to chromatographic stationary phases, and these phases are incorporated into chromatography devices, such as columns. The compositions and devices are of use to separate molecular mixtures. 1. A method of separating analytes in a liquid sample , the method comprising: a solid support having an exterior surface;', 'a ligand comprising a polyhedral oligomeric silsesquioxane moiety;', 'a linker covalently bound to both the polyhedral oligomeric silsesquioxane moiety and the exterior surface of the solid support, wherein the polyhedral oligomeric silsesquioxane moiety is not a cross-linker., 'flowing the liquid sample through a chromatography column configured for use in liquid chromatography, the chromatography column containing therein a composition, the composition comprising2. The method of claim 1 , wherein the liquid sample comprises anions claim 1 , cations claim 1 , and uncharged molecules claim 1 , each retained by the composition.3. The method of claim 1 , wherein the linker comprises at least 4 carbon atoms in sequence.4. The method of claim 1 , wherein the linker comprises at least 8 carbon atoms in sequence.5. The method of claim 1 , wherein the linker comprises at least 10 carbon atoms in sequence.6. The method of claim 3 , wherein the linker comprises at least one heteroatom selected from N claim 3 , O claim 3 , S and a combination thereof.7. The method of claim 3 , wherein the linker comprises a first component and a second component where a linkage fragment joins the first component and the second component claim 3 , in which the linkage fragment is sulfur claim 3 , and the first component and the second component are each an unsubstituted alkyl.8. The method of claim 1 , wherein the solid support is in particulate form claim 1 , and wherein multiple support particles are disposed in a packed bed.9. The method of claim 1 , wherein the ...

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02-03-2017 дата публикации

Functionalized Support Material and Methods of Making and Using Functionalized Support Material

Номер: US20170056854A1
Автор: Feng Gu
Принадлежит: WR Grace and Co Conn

Methods of making functionalized support material are disclosed. Functionalized support material suitable for use in chromatography columns or cartridges, such as in a high pressure liquid chromatography (HPLC) column or a fast protein liquid chromatography (FPLC) column, is also disclosed. Chromatography columns or cartridges containing the functionalized support material, and methods of using functionalized support material, such as a media (e.g., chromatographic material) in a chromatography column or cartridge, are also disclosed.

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28-02-2019 дата публикации

POROUS CYCLODEXTRIN POLYMERIC MATERIALS AND METHODS OF MAKING AND USING SAME

Номер: US20190060868A1
Принадлежит:

A nucleophilic substitution reaction to crosslink cyclodextrin (CD) polymer with rigid aromatic groups, providing a high surface area, mesoporous CD-containing polymers (P-CDPs). The P-CDPs can be used for removing organic contaminants from water. By encapsulating pollutants to form well-defined host-guest complexes with complementary selectivities to activated carbon (AC) sorbents. The P-CDPs can rapidly sequester pharmaceuticals, pesticides, and other organic micropollutants, achieving equilibrium binding capacity in seconds with adsorption rate constants 15-200 times greater than ACs and nonporous CD sorbents. The CD polymer can be regenerated several times, through a room temperature washing procedure, with no loss in performance. 1. A mesoporous polymeric material comprising one or more cyclodextrins crosslinked with at least an equimolar amount of one or more aryl compounds that can react with a cyclodextrin to form an aryl ether bond , wherein the one or more aryl compounds are substituted with 2 or more chloride groups.2. The mesoporous polymeric material of claim 1 , wherein the one or more aryl compounds are substituted with 2-4 chloride groups.3. The mesoporous polymeric material of claim 1 , wherein the one or more aryl compounds comprise C-Chydrocarbon aryl or heteroaryl rings substituted with 2 or more chloride groups.4. The mesoporous polymeric material of claim 1 , wherein the one or more aryl compounds comprise phenyl substituted with 2 or more chloride groups.5. The mesoporous polymeric material of claim 3 , wherein the one or more aryl compounds is a chloro-substituted terephthalonitrile.6. The mesoporous polymeric material of claim 2 , wherein the one or more aryl compounds further comprise one or more electron-withdrawing groups selected from the group consisting of —F claim 2 , —NO claim 2 , and —CN.7. The mesoporous polymeric material of claim 3 , wherein the one or more aryl compounds further comprise one or more electron-withdrawing groups ...

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28-02-2019 дата публикации

CHROMATOGRAPHY LIGAND COMPRISING DOMAIN C FROM STAPHYLOCOCCUS AUREUS PROTEIN A FOR ANTIBODY ISOLATION

Номер: US20190060869A1
Принадлежит: GE Healthcare BioProcess R&D AB

The present invention relates to a chromatography ligand, which comprises Domain C from protein A (SpA), or a functional fragment or variant thereof. The chromatography ligand presents an advantageous capability of withstanding harsh cleaning in place (CIP) conditions, and is capable of binding Fab fragments of antibodies. The ligand may be provided with a terminal coupling group, such as arginine or cysteine, to facilitate its coupling to an insoluble carrier such as beads or a membrane. The invention also relates process of using the ligand in isolation of antibodies, and to a purification protocol which may include washing steps and/or regeneration with alkali. 126-. (canceled)27. A process for isolating one or more target compound(s) , the process comprising: (i) a solid support; and', '(ii) at least one ligand coupled to the solid support, the ligand comprising at least two polypeptides, wherein the amino acid sequence of each polypeptide comprises at least 55 contiguous amino acids of a modified SEQ ID NO. 1, and wherein the modified SEQ ID NO. 1 has an alanine (A) instead of glycine (G) at a position corresponding to position 29 of SEQ ID NO. 1; and, '(a) contacting a first liquid with a chromatography matrix, the first liquid comprising the target compound(s) and the chromatography matrix comprising(b) adsorbing the target compound(s) to the ligand.28. The process of claim 27 , further comprising (c) eluting the compound(s) by passing a second liquid through the chromatography matrix that releases the compound(s) from the ligand.29. The process of claim 27 , wherein the ligand comprises 2-8 of the polypeptides claim 27 , optionally coupled via linker segments.30. The process of claim 27 , wherein the chromatography matrix has retained at least 95% of its original binding capacity after 5 hours incubation in 0.5 M NaOH.31. The process of claim 27 , wherein the ligand binds to the Fab part of an antibody.32. The process of claim 27 , wherein the ligand ...

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17-03-2022 дата публикации

SORBENT USED TO IMPROVE CHROMATOGRAPHIC SEPARATIONS IN SIZE EXCLUSION CHROMATOGRAPHY VIA REDUCED SECONDARY INTERACTIONS

Номер: US20220080388A1
Принадлежит: WATERS TECHNOLOGIES CORPORATION

The present disclosure is directed to stationary phase materials (e.g., porous inorganic-organic hybrid particles) for performing size exclusion chromatography. Embodiments of the present disclosure feature hydroxy-terminated polyethylene glycol surface modified stationary phase materials. 1. A stationary phase material comprising porous particles having a surface , at least some substantial portion thereof modified with a hydroxy-terminated polyethylene glycol , wherein the porous particles comprise an inorganic-organic hybrid material.2. The stationary phase material of claim 1 , wherein the porous particles comprise inorganic-organic hybrid ethylene bridged particles having an empirical formula of SiO(OSiCHCHSiO).3. The stationary phase material of claim 1 , wherein the porous particles have a diameter with a mean size distribution from about 1 to about 50 μm.4. The stationary phase material of claim 1 , wherein the porous particles have a diameter with a mean size distribution from about 1 to about 20 μm.5. The stationary phase material of claim 1 , wherein the porous particles have a diameter with a mean size distribution from about 1.5 to about 5 μm.6. The stationary phase material of claim 1 , wherein the porous particles have an average pore size from about 40 to about 1000 Å claim 1 , from about 100 to about 500 Å claim 1 , or from about 100 to about 300 Å.8. The stationary phase material of claim 7 , wherein m is 2 or 3.9. The stationary phase material of claim 7 , wherein n is from about 5 to about 15 claim 7 , or from about 8 to about 12.10. The stationary phase material of claim 7 , wherein m is 3 and n is from about 8 to about 12.11. The stationary phase material of claim 1 , wherein the hydroxy-terminated polyethylene glycol is present on the surface of the porous particles at a density from about 0.5 to about 15 μmol/m.12. The stationary phase material of claim 11 , wherein the hydroxy-terminated polyethylene glycol is present on the surface of the ...

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09-03-2017 дата публикации

NOVEL AFFINITY CHROMATOGRAPHY MEDIA FOR REMOVAL OF ANTI-A AND/OR ANTI-B ANTIBODIES

Номер: US20170066839A1
Принадлежит:

Embodiments described herein relate to novel chromatography media for removing anti-A and/or anti-B antibodies from a sample, as well as methods of using the same. The media described herein have several advantages over previously described media including, acid and alkaline stability. 1. A media for removing anti-A antibodies from a sample , the media comprising a solid support with a blood group A antigen ligand attached thereto , wherein the ligand is attached to the solid support at a ligand loading of at least 0.8 mg/ml of solid support , and wherein the media is stable under acid and/or alkaline conditions.2. A media for removing anti-B antibodies from a sample , the media comprising a solid support with a blood group B antigen ligand attached thereto , wherein the ligand is attached to the solid support at a ligand loading of at least 0.8 mg/ml of solid support , and wherein the media is stable under acid and/or alkaline conditions.3. The media according to claim 1 , wherein the ligand loading is at least 1 mg/ml of solid support or at least 1.5 mg/ml of solid support or at least 1.65 mg/ml of solid support.4. The media according to claim 2 , wherein the ligand loading is at least 1 mg/ml of solid support or at least 1.2 mg/ml of solid support.5. A media for removing anti-A and anti-B antibodies from a sample claim 2 , the media comprising: (a) a solid support with both blood group A antigen ligand and blood group B antigen ligand attached thereto claim 2 , each at a ligand loading of at least 0.8 mg/ml of solid support; or (b) a mixture of two solid supports claim 2 , one comprising blood group A antigen ligand thereto and another comprising blood group B antigen ligand claim 2 , each media having ligand loading of at least 0.8 mg/ml of solid support claim 2 , wherein the media are stable under acid and/or alkaline conditions.6. The media of claims 1 , wherein the solid support comprises a polymer selected from the group consisting of polyvinylether claims 1 ...

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05-06-2014 дата публикации

Chemically Modified Graphene

Номер: US20140154770A1

This disclosure relates to graphene derivatives, as well as related devices including graphene derivatives and methods of using graphene derivatives. 1. A material , comprising:a graphene derivative comprising a graphene core and a first pendant group, the first pendant group comprising a metal ion, a nanoparticle, a sulfonate group, an amine group, a quaternary ammonium group, or a chelating group.2. The material of claim 1 , wherein the first pendant group comprises a metal ion.3. The material of claim 2 , wherein the first pendant group comprising a linking group and the metal ion is complexed with the linking group.4. The material of claim 3 , wherein the linking group comprises a nitrilotriacetic acid moiety claim 3 , a tris-nitrilotriacetic acid moiety claim 3 , or an iminodiacetic acid moiety.5. The material of claim 3 , wherein the linking group is covalently bonded to the graphene core through an amide group.6. The material of claim 3 , wherein the first pendant group further comprises a His-tagged protein binding to the metal ion.7. The material of claim 6 , wherein the His-tagged protein is His-tagged Protein A or His-tagged Protein G.8. The material of claim 2 , wherein the metal ion is Ni claim 2 , Cu claim 2 , Zn claim 2 , Ag claim 2 , Fe claim 2 , Ga claim 2 , Zr claim 2 , Ca claim 2 , or Co.9. The material of claim 1 , wherein the first pendant group comprises a nanoparticle.10. The material of claim 9 , wherein the nanoparticle is a TiOnanoparticle or a SiOnanoparticle.11. The material of claim 10 , wherein the nanoparticle is a SiOnanoparticle covalently bonded to the graphene core through an amide group.12. The material of claim 11 , wherein the SiOnanoparticle is covalently bonded to the graphene core through a linkage —CO—NH—R—Si(—O—) claim 11 , in which R is C-Calkylene.13. The material of claim 10 , wherein the graphene derivative further comprises a second pendant group claim 10 , the second pendant group comprising metal ion or a ...

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18-03-2021 дата публикации

QUANTUM DOT BEAD HAVING MULTIFUNCTIONAL LIGAND, AND TARGET ANTIGEN DETECTION METHOD AND BIO-DIAGNOSTIC APPARATUS USING SAME

Номер: US20210080454A1
Принадлежит: ZEUS CO., LTD.

In one aspect, the present disclosure relates to a quantum dot bead comprising a multifunctional ligand having a first binding material and a second antibody, and an immunochromatographic detection method for a target antigen in a biological sample, comprising forming multiple bonds with a quantum dot having a second binding material. In addition, the present disclosure has the effect of remarkably amplifying the detection intensity and significantly improving the detection sensitivity without a separate washing step, and thus enables the detection and diagnosis of physiological materials in a biological sample even in an actual product, and may be used to provide a product with excellent competitiveness in price. 1. An immunochromatographic detection method for a target antigen in a biological sample , comprising:forming multiple bonds between a quantum dot bead including a multifunctional ligand having a first binding material and a second antibody, and a quantum dot having a second binding material,wherein the first binding material and the second binding material react to bind to each other, and the second antibody is specific for a target antigen.2. The method of claim 1 , comprising:(a) binding a target antigen in a biological sample with a quantum dot bead; and(b) forming multiple bonds between the quantum dot bead and quantum dots by bonding a first binding material and a second binding material.3. The method of claim 2 , further comprising:after Step (b), Step (c) measuring fluorescence by UV irradiation.4. The method of claim 1 , wherein the first binding material and the multifunctional ligand are covalently bonded.5. The method of claim 1 , wherein the multifunctional ligand is a polymer; a nucleotide chain; or a peptide chain.6. The method of claim 5 , wherein the multifunctional ligand has one or more substituents selected from the group consisting of a hydroxyl group claim 5 , an amine group claim 5 , a thiol group claim 5 , a carbonyl group claim 5 , ...

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23-03-2017 дата публикации

Mutated Immunoglobulin-Binding Protein

Номер: US20170080358A1
Автор: HOBER SOPHIA
Принадлежит:

The present invention relates to an immunoglobulin-binding protein, wherein at least one asparagine residue has been mutated to an amino acid other than glutamine or aspartic acid, which mutation confers an increased chemical stability at pH-values of up to about 13-14 compared to the parental molecule. The protein can for example be derived from a protein capable of binding to other regions of the immunoglobulin molecule than the complementarity determining regions (CDR), such as protein A, and preferably the B-domain of Staphylococcal protein A. The invention also relates to a matrix for affinity separation, which comprises an immunoglobulin-binding protein as ligand coupled to a solid support, in which protein ligand at least one asparagine residue has been mutated to an amino acid other than glutamine. 1. A matrix for affinity chromatography , comprising a plurality of ligands coupled to a solid support , wherein the ligands comprise an immunoglobulin-binding protein , or multimer thereof , capable of binding to other regions of the immunoglobulin molecule than the complementarity determining regions (CDR) , wherein at least two asparagine residues excluding asparagine 21 of a parental immunoglobulin-binding protein defined by SEQ ID NO. 1 or 2 have been mutated to the same or different amino acid residues selected from G , A , V , L , I , S , T , M , F , Y , W , E , R H , or K , which mutations have conferred an increased chemical stability at alkaline pH-values compared to the parental molecule.2. The matrix of claim 1 , wherein the ligands have been coupled to the support by thioether bonding.3. The matrix of claim 1 , wherein the support is a natural polymer material.4. The matrix of claim 1 , wherein the support is a polysaccharide.5. The matrix of claim 1 , which selectively binds an immunoglobulin selected from the group consisting of IgG claim 1 , IgA claim 1 , and IgM.6. The matrix of claim 5 , which selectively binds an IgG immunoglobulin.7. The matrix ...

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22-03-2018 дата публикации

FUNCTIONALIZED SUPPORT FOR ANALYTICAL SAMPLE PREPARATION

Номер: US20180080858A1
Принадлежит:

Aspects of the present disclosure include a solid phase sorbent for preparation of analytical samples. The solid phase sorbent includes particles that are surface modified with an α-cyclodextrin moiety. Also provided is a method of reducing matrix effects in an analytical sample. In some embodiments, the method includes contacting a sample comprising a matrix-interfering agent and an analyte with α-cyclodextrin modified particles to produce a contacted sample wherein the matrix-interfering agent binds to the α-cyclodextrin modified particles; separating the α-cyclodextrin modified particles from the contacted sample to produce a matrix-reduced composition; and detecting the analyte in the matrix-reduced composition. Systems for practicing the subject methods are provided that include the subject solid phase sorbent. 1. A solid phase sorbent for preparation of analytical samples , comprising particles that are surface modified with an α-cyclodextrin moiety.2. The solid phase sorbent of claim 1 , wherein the α-cyclodextrin moiety is linked to the surface of the silica particles via a carbamate claim 1 , a thiocarbamate claim 1 , an ester claim 1 , an amide claim 1 , a thioamide claim 1 , a urea claim 1 , a thiourea claim 1 , an amino claim 1 , a keto claim 1 , or an ether linking group.4. The solid phase sorbent of claim 1 , wherein the α-cyclodextrin moiety comprises 6-hydroxyl-linked claim 1 , 3-hydroxyl linked and/or 2-hydroxyl linked α-cyclodextrin.5. The solid phase sorbent of claim 1 , wherein the α-cyclodextrin moiety is a modified α-cyclodextrin.7. The solid phase sorbent of claim 6 , wherein:the particles are silica particles;{'sup': 1', '2, 'sub': '2', 'Zand Zare independently selected from —N(R′)C(═O)—, —N(R′)C(═O)O—, —N(R′)C(═S)—, —N(R′)C(═S)O—, —N(R′)C(═O)N(R′)—, —N(R′)C(═S)N(R′)—, —CO—, —CO—, — NR′—, and —O— wherein each R′ is independently H, a lower alkyl or a substituted lower alkyl;'}{'sub': 1', '1', '20', '1', '20', '1', '20', '1', '20', '1', '20', ...

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12-03-2020 дата публикации

MUTATED IMMUNOGLOBULIN-BINDING POLYPEPTIDES

Номер: US20200079878A1
Принадлежит:

An Fc-binding polypeptide of improved alkali stability, comprising a mutant of an Fc-binding domain of Protein A (SpA), as defined by SEQ ID NO: 1, SEQ ID NO: 2, SEQ ID NO:3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO:6, SEQ ID NO:7, SEQ ID NO:22, SEQ ID NO 51 or SEQ ID NO 52 wherein at least the asparagine or serine residue at the position corresponding to position 11 in SEQ ID NO:4-7 has been mutated to an amino acid selected from the group consisting of glutamic acid, lysine, tyrosine, threonine, phenylalanine, leucine, isoleucine, tryptophan, methionine, valine, alanine, histidine and arginine. 149-. (canceled)50. A separation matrix comprising: [{'i': 'Staphylococcus', 'a) a mutant of an Fc-binding domain of Protein A (SpA) having the amino acid sequence of SEQ ID NO: 52, wherein the amino acid residue at the position corresponding to position 5 in SEQ ID NO: 52 is alanine, or a variant of the mutant having at least 90% identity thereto; and'}, 'b) a linker comprising 5-10 amino acids coupled to the mutant,', 'wherein linker is free of proline, asparagine, and glutamine; and, 'an Fc-binding polypeptide, wherein the polypeptide comprisesa solid support comprising crosslinked agarose, wherein the Fc-binding polypeptide is coupled to the solid support.51. The separation matrix of claim 50 , wherein the IgG capacity of the matrix after 24 h incubation in 0.5 M NaOH at 22+/−2° C. is at least 95% of the IgG capacity before the incubation.52. The separation matrix of claim 50 , wherein the polypeptide coupling to the solid support comprises a bridge coupling between at least one coupling amino acid on the polypeptide and an electrophilic group on the support.53. The separation matrix of claim 52 , wherein the bridge coupling comprises a thioether bond.54. The separation matrix of claim 52 , wherein the coupling amino acid is selected from one or more of cysteine claim 52 , lysine claim 52 , or histidine.55. The separation matrix of claim 52 , wherein the coupling is ...

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21-03-2019 дата публикации

PEPTOID AFFINITY LIGANDS

Номер: US20190085022A1
Принадлежит:

Disclosed herein are peptoids and related compounds, including peptoid affinity ligands, and hybrid peptoids, for binding and/or purifying immunoglobulins, immunoglobulin fragments or immunoglobulin fusion proteins thereof. Methods of making peptoid affinity ligands and using the same to bind, purify and/or isolate immunoglobulins and related compounds are also disclosed. Such peptoid affinity ligands comprise a peptoid compound consisting of sequentially coupled peptoid residues forming a peptoid backbone, with one or more functional groups appended to a Nitrogen of the peptoid residues of the peptoid backbone configured to provide the desired binding affinity. The peptoids can further comprise a peptoid backbone with at least one functional group coupled to an alpha carbon (C) of a peptide bond in the peptoid backbone thereby forming a hybrid peptoid. 1. A peptoid affinity ligand , the peptoid affinity ligand comprising:a peptoid compound consisting of sequentially coupled peptoid residues forming a peptoid backbone, with one or more functional groups appended to a Nitrogen of the peptoid residues of the peptoid backbone;wherein the one or more functional groups comprise, in any order but coupled to sequential peptoid residues on the peptoid backbone: at least two aromatic functional groups and either a basic or acidic functional group;wherein the peptoid backbone comprises at least one functional group coupled to an alpha carbon (C) of a peptide bond within the peptoid backbone;subject to the proviso that excluded therefrom are peptoid affinity ligands containing a contiguous segment of three peptoid residues with the following functional groups: (i) a basic residue, (ii) an aromatic residue, and (iii) a basic residue or hydrophilic residue; andwherein the peptoid affinity ligand specifically binds an immunoglobulin, immunoglobulin fragment or immunoglobulin fusion protein thereof, wherein the immunoglobulin, immunoglobulin fragment or immunoglobulin fusion ...

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05-04-2018 дата публикации

POROUS CYCLODEXTRIN POLYMERIC MATERIALS AND METHODS OF MAKING AND USING SAME

Номер: US20180093252A1
Принадлежит:

A nucleophilic substitution reaction to crosslink cyclodextrin (CD) polymer with rigid aromatic groups, providing a high surface area, mesoporous CD-containing polymers (P-CDPs). The P-CDPs can be used for removing organic contaminants from water. By encapsulating pollutants to form well-defined host-guest complexes with complementary selectivities to activated carbon (AC) sorbents. The P-CDPs can rapidly sequester pharmaceuticals, pesticides, and other organic micropollutants, achieving equilibrium binding capacity in seconds with adsorption rate constants 15-200 times greater than ACs and nonporous CD sorbents. The CD polymer can be regenerated several times, through a room temperature washing procedure, with no loss in performance. 2. The method of claim 1 , wherein the aryl fluoride is selected from the group consisting of tetrafluoroterephthalonitrile claim 1 , decafluorobiphenyl claim 1 , octafluoronaphthalene claim 1 , and combinations thereof.3. The method of claim 1 , wherein the aryl fluoride comprises tetrafluoroterephthalonitrile.4. The method of claim 1 , wherein the aryl fluoride comprises decafluorobiphenyl.5. The method of claim 1 , wherein the aryl fluoride comprises octafluoronaphthalene.6. The method of claim 1 , wherein the cyclodextrin is β-cyclodextrin.7. The method of claim 2 , wherein the cyclodextrin is β-cyclodextrin.8. The method of claim 3 , wherein the cyclodextrin is β-cyclodextrin.9. The method of claim 4 , wherein the cyclodextrin is β-cyclodextrin.10. The method of claim 5 , wherein the cyclodextrin is β-cyclodextrin.11. The method of claim 1 , wherein the beverage is a fruit juice.12. The method of claim 2 , wherein the fruit juice is orange juice.13. The method of claim 1 , wherein said contacting is for a time sufficient to substantially remove the flavorant from the beverage.14. The method of claim 1 , wherein the flavorant is a compound that impacts the palatability of the beverage.15. The method of claim 13 , wherein the ...

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05-04-2018 дата публикации

ADSORPTIVE MEMBRANES FOR TRAPPING VIRUSES

Номер: US20180094247A1
Автор: Etzel Mark R.
Принадлежит: WISCONSIN ALUMNI RESEARCH FOUNDATION

A disposable, virus-trapping membrane, and a corresponding method to remove viruses from solution are described. The membrane includes a disposable, micro-porous filter membrane and a ligand immobilized on the membrane. The ligand irreversibly and selectively binds viruses. The ligand also has a pKa sufficiently high to repel antibodies via electrostatic charge repulsion. 122-. (canceled)23. A disposable , virus-trapping membrane comprising:a disposable, micro-porous filter membrane; anda multi-modal anion-exchange ligand that has a pKa sufficiently high to repel basic proteins via electrostatic charge repulsion immobilized on the filter membrane, wherein the ligand comprises one or more of tyrosinol, tryptophanol, octopamine, 1,3-diamino-2-hydroxypropane, tris(2-aminoethyl)amine, and agmatine, (a) binds neutral viruses; and', '(b) yields a log-reduction value (LRV) of at least 1.0 for the neutral viruses disposed in a solution comprising 50 mM salt., 'wherein the virus-trapping membrane24. The virus-trapping membrane of claim 23 , wherein the ligand comprises one or more of tryptophanol claim 23 , tris(2-aminoethyl)amine claim 23 , and agmatine claim 23 , and wherein the virus-trapping membrane is dimensioned and configured to yield a log-reduction value (LRV) of at least 1.0 for neutral viruses disposed in a solution comprising 150 mM salt.25. The virus-trapping membrane of claim 23 , wherein the ligand comprises one or more of tris(2-aminoethyl)amine and agmatine claim 23 , and wherein the virus-trapping membrane is dimensioned and configured to yield a log-reduction value (LRV) of at least 5.0 for neutral viruses disposed in a solution comprising 50 mM salt.26. The virus-trapping membrane of claim 23 , wherein the ligand comprises one or more of tris(2-aminoethyl)amine and agmatine claim 23 , and wherein the virus-trapping membrane is dimensioned and configured to yield a log-reduction value (LRV) of at least 5.0 for neutral viruses disposed in a solution ...

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04-04-2019 дата публикации

Super Absorbent Polymer And Method For Producing Same

Номер: US20190099739A1
Принадлежит: LG CHEM, LTD.

The present invention relates to a super absorbent polymer exhibiting more improved absorption under pressure and liquid permeability, even while basically maintaining excellent centrifuge retention capacity and absorption rate, and a method for producing the same. The super absorbent polymer comprises: a base polymer powder including a first crosslinked polymer of a water-soluble ethylenically unsaturated monomer having at least partially neutralized acidic groups; and a surface crosslinked layer formed on the base polymer powder and including a second crosslinked polymer in which the first crosslinked polymer is further crosslinked via a surface crosslinking agent, wherein the surface crosslinking agent includes at least two compounds having a solubility parameter value (σ) of 12.5 (cal/cm)or more, and wherein at least one of the surface crosslinking agents is an alkylene carbonate-based compound, and the remainder is selected from the group consisting of an alkylene carbonate-based compound and a polyhydric alcohol-based compound. 1. A super absorbent polymer comprising:a base polymer powder including a first crosslinked polymer of a water-soluble ethylenically unsaturated monomer having at least partially neutralized acidic groups; anda surface crosslinked layer formed on the base polymer powder and including a second crosslinked polymer in which the first crosslinked polymer is further crosslinked via a surface crosslinking agent,{'sup': 3', '1/2, 'wherein the surface crosslinking agent includes at least two compounds having a solubility parameter value (σ) of 12.5 (cal/cm)or more,'}wherein at least one of the surface crosslinking agents is an alkylene carbonate-based compound, and the remainder is selected from the group consisting of an alkylene carbonate-based compound and a polyhydric alcohol-based compound, and {'br': None, 'i': T', '−T, 'sub': S', '0, 'Permeability (sec)=\u2003\u2003[Equation 1]'}, 'wherein the permeability measured and calculated by the ...

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21-04-2016 дата публикации

SOLID SUPPORT INCLUDING A POLYMER AND USE THEREOF

Номер: US20160107141A1
Принадлежит:

A solid support with a polymer, and a method of using the solid support are provided. 2. The solid support of claim 1 , wherein the fluorocarbon is a substituted or unsubstituted claim 1 , linear or branched compound of fluoro-containing C.3. The solid support of claim 1 , wherein the fluorocarbon is a fluoro-containing Calkyl compound claim 1 , a fluoro-containing Ccarbonyl compound claim 1 , a fluoro-containing Calkoxy compound claim 1 , or a combination thereof.4. The solid support of claim 1 , wherein the biomolecule is selected from the group consisting of a protein claim 1 , a nucleic acid claim 1 , and a sugar.5. The solid support of claim 1 , wherein the material specifically binding to a biomolecule is selected from the group consisting of a protein claim 1 , a nucleic acid claim 1 , a sugar claim 1 , and a cell.6. The solid support of claim 1 , wherein the material specifically binding to a biomolecule is an antibody claim 1 , an antigen against an antibody claim 1 , a receptor against a ligand claim 1 , a ligand against a receptor claim 1 , a substrate or inhibitor of an enzyme claim 1 , or an enzyme against a substrate or inhibitor.7. The solid support of claim 1 , wherein the material specifically binding to a biomolecule is Protein G claim 1 , Protein A claim 1 , lectin claim 1 , an antibody claim 1 , avidin claim 1 , streptavidin claim 1 , a receptor protein claim 1 , or a combination thereof.8. The solid support of claim 1 , wherein the solid support comprises a bead claim 1 , a plate claim 1 , or a well on which the at least one polymer is immobilized.9. The solid support of claim 1 , wherein about 10% to about 90% of the number of repeating units of the polymer comprises at least one material that specifically binds to a biomolecule.10. The solid support of claim 1 , wherein about 10% to about 90% of the number of repeating units of the polymer comprises a fluorocarbon.11. The solid support of claim 1 , wherein the polymer comprises about 1 to ...

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23-04-2015 дата публикации

SEPARATION MATERIAL COMPRISING SACCHARIDE LIGANDS

Номер: US20150111194A1
Принадлежит: GAMBRO LUNDIA AB

A separation material includes a saccharide bound via a linker to a matrix for enabling the separation from a liquid of substances that selectively bind to saccharide moieties. A method for preparing the material, a method for separating from a liquid substances that selective bind to saccharides, and a device including the separation material are also disclosed. 1. A separation material comprising a saccharide-linker-matrix represented by general formula (I){'br': None, 'sup': 1', '2', '1', '3', '1, 'sub': r', 'n', 'm, 'saccharide-X—R—(R—R)—(R—R)-E-F-matrix\u2003\u2003(I)'}wherein{'sub': '2', 'X represents O, S, CHor NR′, wherein R′ represents H, methyl or a protecting group selected from the group consisting of acetyl (Ac), trifluoroacetyl (TFA), trichloroacetyl, benzoyl (Bz), benzyl (Bn), tert-butyloxycarbonyl (BOC), carbobenzyloxy (Cbz), p-methoxybenzyl carbonyl (Moz), 9-fluorenylmethyloxycarbonyl (FMOC), vinyloxycarbonyl (Voc), allyloxycarbonyl (Alloc), p-methoxybenzyl (PMB), 3,4-dimethoxybenzyl (DMB), p-methoxyphenyl (PMP), triphenylmethyl (Tr), tosyl (Ts) and nosyl (Ns),'}{'sup': '1', 'sub': 1', '10, 'Rrepresents, independently of one another, straight-chain or branched C-Calkyl, wherein the alkyl group can be unsubstituted, or substituted with at least one suitable substituent selected from the group of substituents consisting of halogen, alkyl, alkoxy, haloalkyl, cyano, nitro, amino, hydroxy, thiol, acylamino, alkoxycarbonylamino, haloalkoxycarbonylamino or alkylsulfonylamino,'}{'sup': '2', 'Rindependently of one another represents —CO—NH—, —NH—CO—, —C0-NH—NH—, —NH—NH—CO—, —N═CH—, —CH═N—, —NH—N═CH—, —CH═N—NH— or triazolyl,'}{'sup': '3', 'Rindependently of one another represents —O—, —CO—NH—, —NH—CO—, —N═CH— or —CH═N—,'}r represents 0 or an integer from 1-10,n represents 0 or an integer from 1-600,E represents —NH—, —CO—, —O—, —S—, —N═, —CH═, —NH—NH—, —NH—N═ or triazolyl,{'sub': 2', '2, 'F represents —NH—, ═N—, ═CH—, —CO—, —CH—CH(OH)—, —NH—CH—CH(OH)—, —NH—NH ...

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11-04-2019 дата публикации

MULTIMODAL ADSORPTION MEDIUM WITH MULTIMODAL LIGANDS, METHOD FOR THE PREPARATION AND USE THEREOF

Номер: US20190105632A1
Принадлежит:

The present invention relates to a multimodal adsorption medium, in particular a multimodal chromatography medium, a method for its production, as well as use of the adsorption medium according to the invention or an adsorption medium produced according to the invention for the purification of biomolecules. 2. The multimodal adsorption medium as claimed in claim 1 , wherein the —X—(C═O) group is —NH—(C═O) claim 1 ,3. The multimodal adsorption medium as claimed in claim 1 , wherein the polymeric carrier material C comprises at least one material selected from the group composed of natural or synthetic fibers claim 1 , (polymer) membranes claim 1 , porous claim 1 , polymeric monolithic molded bodies claim 1 , polymer gels claim 1 , films claim 1 , nonwovens and wovens.4. The multimodal adsorption medium as claimed in claim 1 , wherein the multimodal ligands are bound to the surface of the carrier material C via polymeric spacer elements.5. The multimodal adsorption medium as claimed in claim 4 , wherein the polymeric spacer elements are polyamines with at least one primary amino group claim 4 , which as an X—(C═O) bond forms an amide bond with the multimodal ligands claim 4 ,6. The multimodal adsorption medium of claim 1 , wherein the G group is a branched or unbranched Calkyl group or a branched or unbranched Calkenyl group.8. The multimodal adsorption medium as claimed in claim 7 , wherein G denotes a branched or unbranched Calkenyl group.10. A method for producing an adsorption medium as claimed in claim 1 , comprising the following steps:(a) providing a polymeric carrier material C, wherein the carrier material C has at least one —XH group that is reactive with carboxylic acid derivatives while forming a covalent bond —X—(C═O), where X denotes —NR—, —O— or —S— and R denotes alkyl, alkenyl, aryl, heteroaryl or hydrogen; and(b) reacting the at least one —XH group of the polymeric carrier material C with a carboxylic acid derivative as a precursor of a multimodal ...

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05-05-2016 дата публикации

Particle of Modified Silica

Номер: US20160122191A1
Принадлежит:

The present invention relates to a particle of modified silica which comprises a particle of silica which is covalently linked to at least one halohydrin moiety. Furthermore, the present invention relates to a method of preparing the particle of modified silica, a particle of modified silica obtained by such method, use of the particle of modified silica as a stationary phase for chromatography, as well as a separation column for chromatography comprising the particle of modified silica. 1. A particle of modified silica which comprises a particle of silica which is covalently linked to at least one halohydrin moiety.3. The particle of modified silica according to claim 1 , wherein the silica is in the form of a porous particle or a monolithic material.4. The particle of modified silica according to claim 2 , wherein A is chlorine.5. The particle of modified silica according to claim 2 , wherein Rcomprises an aryl moiety.6. The particle of modified silica according to claim 2 , wherein Rcomprises a steroid moiety.7. The particle of modified silica according to claim 2 , wherein Rcomprises R—O—CH— claim 2 , and Ris selected from hydrocarbons having from 1 carbon atom up to 30 carbon atoms.9. The particle of modified silica according to claim 1 , wherein the surface density of the halohydrin moiety to particle of silica is from 0.1 to 4 μmoles/msilica surface.10. A method of preparing a particle of modified silica comprising the steps of reacting a particle of silica and at least one halohydrin compound to form a covalent bond between said particle of silica and said halohydrin compound.12. The method according to claim 10 , wherein the particle of silica is in the form of a porous particle or a monolithic material.13. A particle of modified silica obtainable by the method as claimed in .14. A stationary phase for chromatography comprising the particle of modified silica of .15. A separation column for chromatography comprising the particle of modified silica according ...

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05-05-2016 дата публикации

Chromatographic material and method for preparation thereof

Номер: US20160122368A1

A chromatographic material comprising a zwitterionic ligand covalently bound to a substrate, the ligand preferably has a formula II: wherein R 1 , R 2 , R 3 are independently selected from an oxygen atom that is configured to connect to a substrate atom in the substrate, an oxygen atom that is configured to connect to a silicon atom of an adjacent ligand, a hydroxyl group, a halogen atom, an alkoxy group, a dialkylamino group, an acyl group, an alkyl group, or an aryl group; L 1 , L 2 and L 3 are independently hydrophobic moieties; each containing 2 to 30 carbon atoms, wherein there are at least 10 carbon atoms in the combined chain lengths of L 1 , L 2 and L 3 ; X is an O atom, S atom, amide group or sulfonamide group; n is 0 or 1; R 4 , R 5 are independently selected from a hydrogen atom or a hydrocarbon moiety containing 1 to 20 carbon atoms; and R f is a negatively charged moiety comprising a sulfonic, carboxylic, or phosphonic functional group.

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25-08-2022 дата публикации

Super Absorbent Polymer And Method For Producing Same

Номер: US20220266221A1
Принадлежит: LG CHEM, LTD.

The present invention relates to a super absorbent polymer exhibiting more improved absorption under pressure and liquid permeability, even while basically maintaining excellent centrifuge retention capacity and absorption rate, and a method for producing the same. The super absorbent polymer comprises: a base polymer powder including a first crosslinked polymer of a water-soluble ethylenically unsaturated monomer having at least partially neutralized acidic groups; and a surface crosslinked layer formed on the base polymer powder and including a second crosslinked polymer in which the first crosslinked polymer is further crosslinked via a surface crosslinking agent, wherein the surface crosslinking agent includes at least two compounds having a solubility parameter value (σ) of 12.5 (cal/cm)or more, and wherein at least one of the surface crosslinking agents is an alkylene carbonate-based compound, and the remainder is selected from the group consisting of an alkylene carbonate-based compound and a polyhydric alcohol-based compound. 1. A method for producing a super absorbent polymer comprising the steps of:performing crosslinking polymerization of a water-soluble ethylenically unsaturated monomer having at least partially neutralized acidic groups in the presence of an internal crosslinking agent to form a hydrogel polymer containing a first crosslinked polymer;drying, pulverizing and classifying the hydrogel polymer to form a base polymer power; andheat-treating and surface-crosslinking the base polymer powder in the presence of a surface crosslinking agent to form a super absorbent polymer particle,{'sup': 3', '1/2, 'wherein the surface crosslinking agent includes at least two compounds having a solubility parameter value (σ) of 12.5 (cal/cm)or more,'}wherein at least one of the surface crosslinking agents is an alkylene carbonate-based compound, and the remainder is selected from the group consisting of an alkylene carbonate-based compound and a polyhydric ...

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14-05-2015 дата публикации

CHROMATOGRAPHIC MATERIALS

Номер: US20150133294A1
Принадлежит: WATERS TECHNOLOGIES CORPORATION

In one aspect, the present invention provides a chromatographic stationary phase material for various different modes of chromatography represented by Formula 1: [X](W)(Q)(T)(Formula 1). X can be a high purity chromatographic core composition having a surface comprising a silica core material, metal oxide core material, an inorganic-organic hybrid material or a group of block copolymers thereof. W can be absent and/or can include hydrogen and/or can include a hydroxyl on the surface of X. Q can be a functional group that minimizes retention variation over time (drift) under chromatographic conditions utilizing low water concentrations. T can include one or more hydrophilic, polar, ionizable, and/or charged functional groups that chromatographically interact with the analyte. Additionally, b and c can be positive numbers, with the ratio 0.05≦(b/c)≦100, and a≧0. 1. A chromatographic stationary phase material for normal phase chromatography , high-pressure liquid chromatography , solvated gas chromatography , supercritical fluid chromatography , sub-critical fluid chromatography , carbon dioxide based chromatography , hydrophilic interaction liquid chromatography or hydrophobic interaction liquid chromatography represented by Formula 1:{'br': None, 'sub': a', 'b', 'c, '[X](W)(Q)(T)\u2003\u2003Formula 1'}wherein:X is a high purity chromatographic core composition having a surface comprising a silica core material, metal oxide core material, an inorganic-organic hybrid material or a group of block copolymers thereof;W is absent and/or includes hydrogen and/or includes hydroxyl on the surface of X;Q is a functional group that minimizes retention variation over time (drift) under chromatographic conditions utilizing low water concentrations;T comprises one or more hydrophilic, polar, ionizable, and/or charged functional groups that chromatographically interact with the analyte; andb and c are positive numbers, 0.05≦(b/c)≦100, and a≧0.2. A chromatographic stationary phase ...

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14-05-2015 дата публикации

SEPARATION METHOD AND SEPARATION MATRIX

Номер: US20150133618A1
Принадлежит:

The invention discloses a method of separating a biomolecule from at least one other component in a liquid, comprising a step of contacting said liquid with a separation matrix comprising a solid support and polymer chains bound to said solid support. The polymer chains comprise units derived from a first monomer of structure CH═CH-L-X, where L is a covalent bond or an alkyl ether or hydroxysubstituted alkyl ether chain comprising 2-6 carbon atoms, and X is a sulfonate or phosphonate group. 1. A method of separating a biomolecule from at least one other component in a liquid , comprising a step of contacting said liquid with a separation matrix comprising a solid support and polymer chains bound to said solid support , wherein said polymer chains comprise units derived from a first monomer of structure CH═CH-L-X , where L is a covalent bond or an alkyl ether or hydroxysubstituted alkyl ether chain comprising 2-6 carbon atoms , and X is a sulfonate or phosphonate group.2. The method of claim 1 , wherein said biomolecule is a protein claim 1 , a peptide or a nucleic acid.3. The method of claim 1 , wherein said biomolecule is an immunoglobulin claim 1 , immunoglobulin fragment or an immunoglobulin-containing protein claim 1 , such as an antibody claim 1 , an antibody fragment claim 1 , an antibody conjugate or an antibody fusion protein.4. The method of claim 1 , wherein said at least other component is a protein claim 1 , such as a host cell protein claim 1 , protein A or an aggregate of immunoglobulins claim 1 , immunoglobulin fragments or immunoglobulin-containing proteins.5. The method of claim 1 , wherein the liquid is an eluate from a previous chromatography step claim 1 , such as an affinity step claim 1 , an ion exchange step claim 1 , a multimodal step or a hydrophobic interaction step.6. The method of claim 1 , wherein the liquid is the flow-through from a separation matrix claim 1 , such as an ion exchange matrix claim 1 , a multimodal matrix or a ...

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23-04-2020 дата публикации

SUPER ABSORBENT POLYMER AND PREPARATION METHOD THEREOF

Номер: US20200122119A1
Принадлежит: LG CHEM, LTD.

The super absorbent polymer according to the present invention has reduced 3-hour saline solution re-wet while having a high absorption rate and absorption against pulp, and thus can be used for hygienic materials such as diapers, thereby exhibiting excellent performance. 1. A super absorbent polymer comprising:a base polymer powder containing a first crosslinked polymer of a water-soluble ethylenically unsaturated monomer having an acidic group in which at least a part thereof is neutralized; anda surface crosslinked layer formed on the base polymer powder and containing a second crosslinked polymer in which the first crosslinked polymer is additionally cross-linked via a surface crosslinking agent,wherein the super absorbent polymer has an absorption rate (vortex) of 50 seconds or less,an absorption against pulp of 15 g/g or more, anda 3-hour saline solution re-wet of 1.0 g or less.2. The super absorbent polymer of claim 1 , wherein it has an absorption rate of 45 seconds or less.3. The super absorbent polymer of claim 1 , wherein it has an absorption against pulp of 18 g/g or more.4. The super absorbent polymer of claim 1 , wherein it has an absorbency under pressure at 0.9 psi (0.9 AUP) of 9 g/g or more.5. The super absorbent polymer of claim 1 , wherein it has a gel bed permeability (GBP) of 9 Darcy or more.6. The super absorbent polymer of claim 1 , wherein it has a centrifuge retention capacity (CRC) of 28 g/g or more.7. A method for preparing a super absorbent polymer comprising the steps of:crosslinking a water-soluble ethylenically unsaturated monomer having an acidic group in which at least a part thereof is neutralized in the presence of an internal crosslinking agent to form a hydrogel polymer containing a first crosslinked polymer;drying, pulverizing and classifying the hydrogel polymer to form a base polymer power; andheat-treating and surface-crosslinking the base polymer powder in the presence of a surface crosslinking solution to form a super ...

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01-09-2022 дата публикации

COMPOSITIONS, KITS AND METHODS USEFUL FOR ANALYZING ANTIBODY-CONTAINING SAMPLES

Номер: US20220275022A1
Принадлежит:

In some aspects, the present disclosure pertains to sample treatment methods that comprise: contacting an acidic elution solution that is free of primary amine, secondary amine and thiol groups with a sorbent having bound target antibody and separating the elution solution from the sorbent, thereby releasing bound target antibody from the sorbent and forming a first collection fraction that comprises the elution solution and released target antibody; contacting the sorbent with a neutralization buffer solution that is free of primary amine, secondary amine and thiol groups and separating the neutralization buffer solution from the sorbent, thereby forming a second collection fraction that comprises the neutralization buffer solution; and forming a neutralized solution that comprises the first collection fraction and the second collection fraction. In other aspects, the present disclosure pertains to kits for performing such sample treatment methods. 1. A sample treatment method comprising:(a) contacting a sample fluid that contains a target antibody with a sorbent that has affinity for the target antibody and separating the sample fluid from the sorbent, thereby forming a sorbent having bound target antibody;(b) contacting a washing solution that is free of primary amine, secondary amine and thiol groups with the sorbent having bound target antibody and separating the washing solution from the sorbent having bound target antibody, thereby removing unbound molecules from the sorbent having bound target antibody while leaving target antibody bound to the sorbent;(c) contacting an acidic elution solution that is free of primary amine, secondary amine and thiol groups with the sorbent and separating the elution solution from the sorbent, thereby releasing bound target antibody from the sorbent and forming a first collection fraction that comprises the elution solution and released target antibody;(d) contacting the sorbent with a neutralization buffer solution that is ...

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03-06-2021 дата публикации

Mutated Immunoglobulin-Binding Polypeptides

Номер: US20210162319A1
Автор: HOBER SOPHIA
Принадлежит:

The present invention relates to an immunoglobulin-binding protein, wherein at least one asparagine residue has been mutated to an amino acid other than glutamine or aspartic acid, which mutation confers an increased chemical stability at pH-values of up to about 13-14 compared to the parental molecule. The protein can for example be derived from a protein capable of binding to other regions of the immunoglobulin molecule than the complementarity determining regions (CDR), such as protein A, and preferably the B-domain of Staphylococcal protein A. The invention also relates to a matrix for affinity separation, which comprises an immunoglobulin-binding protein as ligand coupled to a solid support, in which protein ligand at least one asparagine residue has been mutated to an amino acid other than glutamine. 1. A matrix for affinity chromatography , comprising a plurality of ligands coupled to a solid support ,wherein the ligands comprise an immunoglobulin-binding protein, or multimer thereof that binds to other regions of the immunoglobulin molecule than the complementarity determining regions (CDR), andwherein at least one of N3, N6 and N23 of a parental immunoglobulin-binding protein defined by SEQ ID NOS:1 or 2 have been mutated to amino acid residues selected from A, D, I, S, T, E, or H,wherein the N3, N6 and N23 asparagine residues can be mutated to amino acid residues that are the same or different from each other, andwherein the mutations have conferred an increased chemical stability at alkaline pH-values compared to the parental immunoglobulin-binding protein.2. The matrix of claim 1 , wherein N3 of the parental immunoglobulin-binding protein defined by SEQ ID NOS:1 or 2 has been mutated to an amino acid residue selected from A claim 1 , D claim 1 , I claim 1 , S claim 1 , T claim 1 , E claim 1 , or H.3. The matrix of claim 2 , wherein N3 of the parental immunoglobulin-binding protein defined by SEQ ID NOS:1 or 2 has been mutated to A.4. The matrix of claim ...

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17-05-2018 дата публикации

WATER FILTRATION APPARATUS AND A METHOD OF USING THEREOF

Номер: US20180134582A1
Принадлежит: University of Dammam

A water filtration apparatus and a method of using thereof, wherein the water filtration apparatus includes a nanoparticle layer which comprises polypeptide-functionalized nanoparticles that are capable of absorbing heavy metals selected from the group consisting of Pb, As, Cd, Hg, Cr, Cu, and Zn, as well as organic materials. Various embodiments of the water filtration apparatus, the method of using the apparatus, and a method of producing the polypeptide-functionalized nanoparticles are also provided. 1. A water filtration apparatus , comprising:a hollow filter cartridge having a water inlet and a water outlet;a zeolite layer located inside said cartridge between the water inlet and the water outlet, which is configured to reduce a concentration of heavy metals in water;a nanoparticle layer located between the zeolite layer and the water outlet, which is configured to remove heavy metals and organic compounds in water; andan activated carbon layer located between the zeolite layer and the nanoparticle layer, which is configured to reduce a concentration of organic compounds in water,wherein the nanoparticle layer comprises polypeptide-functionalized nanoparticles.3. The water filtration apparatus of claim 2 , wherein the linker comprises a heterocycle.4. The water filtration apparatus of claim 2 , wherein the linker comprises a triazole.5. The water filtration apparatus of claim 2 , wherein the linker comprises a carbocycle.6. The water filtration apparatus of claim 2 , wherein the linker is bound to the polypeptide via an amide bond.7. The water filtration apparatus of claim 2 , wherein the nanoparticle is a silica nanoparticle.8. The water filtration apparatus of claim 7 , wherein the linker is bound to the silica nanoparticle via a Si—O—Si bond.9. The water filtration apparatus of claim 2 , wherein the polypeptide is a block copolymer comprising at least two polymers selected from the group consisting of an alkyl-functionalized glutamine polymer claim 2 , a ...

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09-05-2019 дата публикации

Method Of Preparing Superabsorbent Polymer

Номер: US20190134603A1
Принадлежит: LG CHEM, LTD.

A superabsorbent polymer according to the present invention has excellent initial absorption properties, and thus it may be used in sanitary materials such as diapers, etc., thereby exhibiting excellent performances. 1. A method of preparing a superabsorbent polymer , the method comprising the following steps of:performing crosslinking polymerization of a water-soluble ethylene-based unsaturated monomer having acidic groups which are at least partially neutralized in the presence of an internal crosslinking agent and a surfactant to form a hydrogel polymer containing a first crosslinked polymer (Step 1);drying, pulverizing, and size-sorting the hydrogel polymer to form a base polymer powder (Step 2); andperforming surface-crosslinking of the base polymer powder by heat treatment in the presence of a surface crosslinking solution to form superabsorbent polymer particles (Step 3),wherein a maximum foaming point reaches within 100 seconds from a polymerization initiation point of the water-soluble ethylene-based unsaturated monomers in Step 1.2. The method of claim 1 , wherein Step 1 is performed additionally in the presence of a foaming agent.3. The method of claim 2 , wherein the foaming agent is one or more selected from the group consisting of sodium bicarbonate claim 2 , sodium carbonate claim 2 , potassium bicarbonate claim 2 , potassium carbonate claim 2 , calcium bicarbonate claim 2 , calcium carbonate claim 2 , magnesium bicarbonate claim 2 , magnesium carbonate claim 2 , 2 claim 2 ,2′-azobis(2-methylpropionamidine) dihydrochloride claim 2 , azodicarbonamide claim 2 , dinitroso pentamethylene tetramine claim 2 , p claim 2 ,p′-oxybisbenzenesulfonylhydrazide claim 2 , and p-toluenesulfonyl hydrazide.4. The method of claim 1 , wherein the surfactant is a compound represented by the following Chemical Formula 2 or sugar ester:{'br': None, 'sub': '3', 'R—SONa\u2003\u2003[Chemical Formula 2]'}in Chemical Formula 2,R is an alkyl group having 8 to 16 carbon atoms.5. ...

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21-08-2014 дата публикации

SILICA SPHERES AND AFFINITY CARRIER

Номер: US20140235435A1
Принадлежит: AGC Si-Tech Co., Ltd.

To provide an affinity carrier with a low pressure loss and a large binding capacity even when the linear flow rate of a solution to be made to pass therethrough is high. 1. Silica spheres , which satisfy the following conditions:(a) the average particle size is from 30 μm to 40 μm as measured by a laser light scattering method;(b) the ratio (D10/D90) of the particle size (D10) of smaller 10% cumulative volume to the particle size (D90) of 90% cumulative volume in a particle size distribution as measured by a Coulter counter method, is at most 1.50; and(c) the average pore size is from 85 nm to 115 nm and the pore volume is at least 1.5 mL/g, as measured by a mercury intrusion technique.2. The silica spheres according to claim 1 , wherein the ratio (D10/D90) of the particle size (D10) of smaller 10% cumulative volume to the particle size (D90) of 90% cumulative volume in the particle size distribution claim 1 , is at most 1.35.3. The silica spheres according to claim 1 , wherein the average particle size is from 33 μm to 37 μm.4. The silica spheres according to claim 1 , which has a specific surface area of from 55 m/g to 75 m/g.5. An affinity carrier comprising the silica spheres as defined in claim 1 , and having a ligand immobilized to the silica spheres.6. The affinity carrier according to claim 5 , wherein the ligand is protein A claim 5 , and the amount of the protein A immobilized is at least 10 mg/mL-bed.7. The affinity carrier according to claim 5 , which has a dynamic binding capacity of at least 50 mg/mL-bed. The present invention relates to silica spheres and an affinity carrier.In recent years, high precision purification or removal of a specific protein is emphasized in medical and pharmaceutical fields. For example, in order to purify a chemical having a specific function, it is necessary to purify a specific protein highly precisely.In affinity chromatography, protein A having a specific binding property as a ligand is widely used. Protein A is a ...

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01-06-2017 дата публикации

PROCESS FOR MANUFACTURING A COMPOSITE SORBENT MATERIAL FOR CHROMATOGRAPHICAL SEPARATION OF BIOPOLYMERS

Номер: US20170152501A1
Принадлежит: NExtTec GmbH

The present invention relates to a sorbent material for separation and purification of biopolymers, particularly nucleic acids, having a solid support substantially modified with a copolymer coating comprising aromatic monomers and crosslinking compounds and unsaturated esters or ethers preferably attached to the support via a vinylchlorsilane. The use of these materials for separation of nucleic acids, particularly a one-step isolation of DNA from lysates of different biological sources, is an object of the invention as well as a chromatographic column or cartridge at least partially filled with the sorbent material of the invention, a membrane-like device comprising the sorbent material of the invention, and a kit comprising the sorbent material of the invention in bulk or packed in chromatographic devices as well as other devices necessary for performing sample preparations. 122-. (canceled)24. The process of wherein the support is a porous inorganic material comprising inorganic metal oxide.25. The process of wherein the porous inorganic metal oxides show a bidisperse distribution of pore sizes.26. The process of wherein the support has an average pore size of 2-200 nm.27. The process of wherein the polymer coating has a thickness of about 10 to 250 Angström.28. The process of wherein the inorganic metal oxide is selected from the group consisting of oxides of aluminum claim 24 , titanium claim 24 , zirconium claim 24 , silicon oxides claim 24 , iron oxides claim 24 , controlled pore glass (CPG) claim 24 , diatomaceous earth and combinations thereof.29. The process of wherein the porous inorganic metal oxide shows a bidisperse distribution with mean pore diameters in the range of 20-100 nm for the larger pore size.30. The process of wherein the porous inorganic metal oxide has a mean pore diameter in the range of 2-15 nm for the smaller pore size.31. The process of wherein the ratio of the mean diameter of the large pore size distribution and the lower pore size ...

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07-06-2018 дата публикации

HIGH PURITY CHROMATOGRAPHIC MATERIALS COMPRISING ION PAIRED-BONDED PHASES FOR SUPERCRITICAL FLUID CHROMATOGRAPHY

Номер: US20180154332A1
Принадлежит:

The present invention provides novel chromatographic materials, e.g., for chromatographic separations, processes for its preparation and separations devices containing the chromatographic material; separations devices, chromatographic columns and kits comprising the same; and methods for the preparation thereof. The chromatographic materials of the invention are high purity chromatographic materials comprising a chromatographic surface wherein the chromatographic surface comprises a covalently-bonded surface group and one or more ionizable modifier. 1. A high purity chromatographic material comprising a chromatographic surface wherein the chromatographic surface comprises an ion-paired bonded moiety.2. The high purity chromatographic material of claim 1 , wherein the chromatographic surface further comprises covalently-bonded surface groups.3. The high purity chromatographic material of claim 1 , wherein the ion-paired bonded moiety is polar.4. The high purity chromatographic material of claim 1 , comprising two or more polar ion-paired bonded moieties such that the net charge on the surface of the material is neutral.5. The high purity chromatographic material of claim 1 , wherein the ion-paired bonded moiety is formed between an ion-pair forming surface group and a counterion.6. The high purity chromatographic material of claim 5 , wherein the ion-paired bonded moiety is formed between a basic ion-pair forming surface group and an acidic counterion.7. The high purity chromatographic material of claim 5 , wherein the ion-paired bonded moiety is formed between an acidic ion-pair forming surface group and a basic counterion.8. The high purity chromatographic material of claim 6 , wherein the basic ion-pair forming surface group is a nitrogen-containing surface group.9. The high purity chromatographic material of claim 6 , wherein the acidic counterion is a sulfonic acid counterion.10. The high purity chromatographic material of claim 6 , wherein basic ion-pair ...

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22-09-2022 дата публикации

FUNCTIONALIZED SUPPORT MATERIAL AND METHODS OF MAKING AND USING FUNCTIONALIZED SUPPORT MATERIAL

Номер: US20220297088A1
Автор: Gu Feng
Принадлежит: W.R.Grace & Co-CONN.

Methods of making functionalized support material am disclosed. Functionalized support material suitable for use in chromatography columns or cartridges, such as in a high pressure liquid chromatography (HPLC) column or a fast protein liquid chromatography (FPLC) column, is also disclosed. Chromatography columns or cartridges containing the functionalized support material, and methods of using functionalized support material, such as a media (e.g., chromatographic material) in a chromatography column or cartridge, are also disclosed. 155-. (canceled)56. A chromatographic material comprising:silica support material and polymer chains extending from a surface of the silica support material, the polymer chains being covalently bonded to the surface through a divalent sulfur bond —S—; [ 2-acrylamido-2-methyl-1-propanesulfonic acid, vinylsulfonic acid, or a combination thereof; or', '2-acrylamido-2-methyl-1-propanesulfonic acid, methacrylic acid, acrylic acid, N,N-diethylaminoethyl acrylate, (3-acrylamidopropyl)-trimethylammonium chloride, diallyldimethylammonium chloride, or a combination of two or more thereof, and, 'the polymer chains comprise the reaction product of a thiol-functionalized silica support and monomers comprising, 'the thio-functionalized silica support is the reaction product of silica particles and (A) an epoxy silane and 1,2-ethanedithiol, or (B) 3-mercaptopropyl-trimethoxysilane., 'wherein57. The chromatographic material of claim 56 , wherein the support material further comprises at least one bifunctional second compound extending from the surface of the support material claim 56 , each of the at least one bifunctional compound comprising (i) one or more functional groups capable of bonding the bifunctional compound to the surface claim 56 , and (ii) one or more hydrophilic groups claim 56 , and/or wherein the functionalized support material comprises a covalent bond linkage between the support material and each of the polymer chains claim 56 , ...

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14-05-2020 дата публикации

Functionalized chromatographic materials and methods of making and using therefor

Номер: US20200147582A1
Принадлежит:

Methods, compositions, devices and kits having a novel chromatographic material are provided herein for separating and identifying organic molecules and compounds, for example molecules and compounds containing electron rich functional groups such as carbon-carbon double bonds. The methods, compositions, and kits include a metal-thiolate chromatographic medium (MTCM) with a sulfur-containing functional group or a metal-selenolate chromatographic medium (MSCM) comprising a selenium-containing functional group covalently attached to a support medium, such that the sulfur-containing functional group or selenium-containing functional group is bound to at least one metal atom. The MTCM and/or MSCM has affinity and specificity to compounds having one or more carbon-carbon double bonds, and performs a highly efficient and rapid separation of samples yielding non-overlapping peaks of purified materials compared to traditional media. 173-. (canceled)74. A separation system comprising: a chromatographic medium comprising atoms of a transition metal selected from the group consisting of copper , gold and a combination thereof , present as a stationary phase in a pipette or column , wherein the chromatographic medium comprises selenium-containing functional group (MSCM) , and wherein the selenium-containing functional group is linked to a support by at least one spacer , and a sample source coupled to the pipette or column comprising a sample to be separated , wherein the sample includes a compound having a functional group.75. The chromatographic medium according to claim 74 , on a support selected from the group consisting of silica gel claim 74 , alumina claim 74 , polystyrene claim 74 , agarose claim 74 , modified polymeric resin claim 74 , cellulose claim 74 , magnesium silicate claim 74 , dextran claim 74 , and starch.76. The chromatographic medium according to claim 74 , configured as an analytical component of a chromatographic separation system selected from: normal ...

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28-08-2014 дата публикации

SORBENT COMPRISING AN AROMATIC RING SYSTEM ON ITS SURFACE FOR THE PURIFICATION OF ORGANIC MOLECULES

Номер: US20140243512A1
Принадлежит: INSTRACTION GMBH

In a first embodiment the present invention relates to a sorbent comprising a porous inorganic solid support material having on its surface a film of a crosslinked polyvinylamine comprising derivatized amine groups and amine groups binding to the surface of the support material via electron donor/acceptor interactions. In a second embodiment the present invention relates to a sorbent comprising a solid support material, the surface of which comprises a residue of a general formula (I), wherein the residue is attached via a covalent single bond to a functional group on the surface of either the bulk solid support material itself or of a polymer film on the surface of the solid support material. Furthermore, the present invention relates to the use of the sorbents according to the invention for the purification of organic molecules, in particular pharmaceutical active compounds, preferably in chromatographic applications. 110-. (canceled)11. A sorbent comprising a porous inorganic solid support material , wherein the surface of the porous inorganic solid support material comprises a film of a crosslinked polyvinylamine comprising derivatized amine groups which are derivatized by a residue which is bound via the amine group , and primary amine groups which bind to the surface of the porous inorganic solid support material via electron donor/acceptor interactions , wherein the ratio of the amount of derivatized amine groups to the amount of primary amine groups binding to the surface is in the range of from 0.33 to 2.33 , wherein the residue comprises an optionally substituted aliphatic hydrocarbon group or an optionally substituted aromatic or heteroaromatic ring system.12. The sorbent of claim 11 , wherein the porous inorganic solid support material comprises silicon oxide.13. The sorbent of claim 11 , wherein the molar amount of derivatized amine groups is in the range of from 25 to 70 mol-% claim 11 , relative to the total amount of non-crosslinked amine groups of ...

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04-09-2014 дата публикации

PALLADIUM SEPARATING AGENT, METHOD FOR PRODUCING SAME AND USE OF SAME

Номер: US20140248198A1
Принадлежит: TOSOH CORPORATION

To provide a palladium separating agent capable of separating palladium ions from a solution containing palladium ions of a low concentration to a high concentration in a short time with a high selectivity, and a method for separating palladium. 1. A palladium separating agent having a functional group represented by the formula (1) bonded to a carrier:{'br': None, 'sub': '2', 'i': 'n', '—Z—(CH)-S—R\u2003\u2003(1)'}{'sub': 1-18', '3-10', '6-14, 'wherein R is a Cchain hydrocarbon group, a Calicyclic hydrocarbon group, a Caromatic hydrocarbon group, a carboxymethyl group or a carboxyethyl group, n is an integer of from 1 to 4, and Z is an amide bond.'}3. The palladium separating agent according to claim 1 , wherein the functional group represented by the formula (1) is bonded to the carrier by means of a methylene group claim 1 , an ethylene group claim 1 , a Clinear claim 1 , branched or cyclic alkylene group or a Carylene group.4. The palladium separating agent according to claim 3 , wherein the functional group represented by the formula (1) is bonded to the carrier by means of a n-propylene group.5. The palladium separating agent according to claim 1 , wherein R in the formula (1) is a methyl group claim 1 , an ethyl group claim 1 , a propyl group claim 1 , a butyl group claim 1 , an isopropyl group claim 1 , a phenyl group or a benzyl group.6. The palladium separating agent according to claim 1 , wherein in the formula (1) claim 1 , n is an integer of 1.7. The palladium separating agent according to claim 1 , wherein the carrier is an inorganic carrier.8. The palladium separating agent according to claim 7 , wherein the inorganic carrier is a silica gel.9. The palladium separating agent according to claim 1 , wherein the element ratio (S/N) of the S element to the N element contained in the palladium separating agent is from 0.94 to 1.00 claim 1 , and the average pore size of the carrier is at least 2 μm.10. A method for producing a palladium separating agent ...

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29-09-2022 дата публикации

MIXED MODE CATION EXCHANGE CHROMATOGRAPHY LIGANDS BASED ON 1,3-DIOXOISOINDOLIN-2-YL STRUCTURES

Номер: US20220305460A1
Принадлежит:

The subject invention pertains to proteins are purified by a mixed-mode chromatography system formed by attaching a ligand with cation exchange and hydrophobic 1,3-droxoisoindolin-2-yl group functionalities to a large-pore support matrix, the only linkage between the ligand and the support matrix being a chain having a backbone of one, two, three, four, or five atoms between the hydrophobic group and the support matrix. 1. A mixed-mode chromatography medium comprising one or more ligand coupled to a solid support , said ligand comprising a 1 ,3-droxoisoindolin-2-yl group , said solid support having pores of a median diameter of 0.5 micron or greater with substantially no pores of 0.1 micron or less in diameter , and said ligand coupled to said solid support at a 1 ,3-droxoisoindolin-2-yl group through a chain of one to five atoms.2. The mixed-mode chromatography medium of claim 1 , wherein the solid support comprises particles and said particles have a median particle size of from about 25 microns to about 150 microns.3. The mixed-mode chromatography medium of claim 1 , wherein the ligand is 2-(5-amino-1 claim 1 ,3-dioxoisoindolin-2-yl)acetic acid claim 1 , 4-(5-amino-1 claim 1 ,3-dioxoisoindolin-2-yl)butanoic acid claim 1 , 2-(4-amino-1 claim 1 ,3-dioxoisoindolin-2-yl)acetic acid claim 1 , and/or 4-(4-amino-1 claim 1 ,3-dioxoisoindolin-2-yl)butanoic acid.4. The mixed-mode chromatography medium of claim 1 , wherein the mixed-mode chromatography medium has a dynamic binding capacity of at least about 30 mg of IgG per mL of mixed-mode chromatography medium.5. A composition comprising the mixed-mode chromatography medium of and a source solution or a buffer.6. The composition of claim 5 , wherein the source solution comprises non-antibody target proteins claim 5 , monomeric antibodies and/or antibody aggregates.7. The composition of claim 5 , wherein said source solution or buffer contains a salt selected from alkali metal and alkaline earth metal halides at a ...

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30-05-2019 дата публикации

COMPOSITE MATERIALS IN WOUND TREATMENT

Номер: US20190160197A1
Принадлежит:

The present invention relates to a composite material, which is of particular use in wound treatment, and to a method for producing the same composite material. Said composite material comprises a hydrophilic polyurethane foam material comprising a first polyurethane polymer; a hydrophilic fiber material comprising a second polymer, wherein said second polymer is not a polyurethane polymer and wherein said fiber material is capable of absorbing and retaining a fluid. In the composite material according to the present invention, said first polymer is covalently bonded to said second polymer. 1. A composite material comprising:a hydrophilic polyurethane foam material comprising a first polyurethane polymer;a hydrophilic fiber material comprising a second polymer, wherein said second polymer is not a polyurethane polymer;wherein said fiber material is capable of absorbing and retaining a fluid,wherein said hydrophilic polyurethane foam material is comprised in a foam layer, and said hydrophilic fiber material is comprised in a fiber layer, wherein the thickness of said foam layer and/or said fiber layer, independently, is at least 100 μm, andwherein said first polyurethane polymer is covalently bonded to said second polymer.2. The composite material according to claim 1 , wherein said first polymer is covalently bonded to said second polymer by at least one urethane linkage or at least one urea linkage claim 1 , wherein said urethane linkage or said urea linkage is derived from a reaction between at least one hydroxyl group or at least one amine group claim 1 , respectively claim 1 , of said second polymer of said hydrophilic fiber material and at least one isocyanate group of a prepolymer as used to obtain said first polyurethane polymer of said hydrophilic polyurethane foam material.3. The composite material according to claim 1 , wherein said hydrophilic fiber material comprises a non-woven material.4. The composite material according to claim 1 , wherein the ...

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22-06-2017 дата публикации

Porous cyclodextrin polymeric materials and methods of making and using same

Номер: US20170173560A1
Принадлежит: CORNELL UNIVERSITY

A nucleophilic substitution reaction to crosslink cyclodextrin (CD) polymer with rigid aromatic groups, providing a high surface area, mesoporous CD-containing polymers (P-CDPs). The P-CDPs can be used for removing organic contaminants from water. By encapsulating pollutants to form well-defined host-guest complexes with complementary selectivities to activated carbon (AC) sorbents. The P-CDPs can rapidly sequester pharmaceuticals, pesticides, and other organic micropollutants, achieving equilibrium binding capacity in seconds with adsorption rate constants 15-200 times greater than ACs and nonporous CD sorbents. The CD polymer can be regenerated several times, through a room temperature washing procedure, with no loss in performance.

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22-06-2017 дата публикации

HYBRID MATERIAL FOR CHROMATOGRAPHIC SEPARATIONS COMPRISING A SUPERFICIALLY POROUS CORE AND A SURROUNDING MATERIAL

Номер: US20170173561A1
Принадлежит:

The present invention provides novel chromatographic materials, e.g., for chromatographic separations, processes for their preparation and separations devices containing the chromatographic materials. The preparation of the inorganic/organic hybrid materials of the invention wherein a surrounding material is condensed on a superficially porous hybrid core material will allow for families of different hybrid packing materials to be prepared from a single core hybrid material. Differences in hydrophobicity, ion-exchange capacity, chemical stability, surface charge or silanol activity of the surrounding material may be used for unique chromatographic separations of small molecules, carbohydrates, antibodies, whole proteins, peptides, and/or DNA. 1. An inorganic/organic hybrid material comprising an inorganic/organic hybrid surrounding material and a superficially porous core.28.-. (canceled)9. The inorganic/organic hybrid material of claim 1 , wherein the inorganic/organic surrounding material is derived fromcondensation of one or more polymeric organofunctional metal precursors, and/or polymeric metal oxide precursors on the surface of the superficially porous core, orapplication of partially condensed polymeric organofunctional metal precursors, a mixture of two or more polymeric organofunctional metal precursors, or a mixture of one or more polymeric organofunctional metal precursors with a polymeric metal oxide precursors on the surface of the superficially porous core.10. The inorganic/organic hybrid material of claim 9 , wherein the inorganic portion of the inorganic/organic surrounding material is selected from the group consisting of alumina claim 9 , silica claim 9 , titania claim 9 , cerium oxide claim 9 , or zirconium oxides claim 9 , and ceramic materials.11. The inorganic/organic hybrid material of claim 10 , wherein the inorganic portion of the inorganic/organic surrounding material is silica.12. The inorganic/organic hybrid material of claim 1 , wherein ...

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06-06-2019 дата публикации

NOVEL GRAFT POLYMER, TEMPERATURE-RESPONSIVE SUBSTRATE FOR CELL CULTURE USING THE SAME AND PRODUCTION METHOD THEREFOR, AS WELL AS LIQUID CHROMATOGRAPHIC CARRIER HAVING THE NOVEL GRAFT POLYMER IMMOBILIZED THEREON AND LIQUID CHROMATOGRAPHIC METHOD USING THE SAME

Номер: US20190169567A1
Принадлежит:

By using a graft polymer comprising a dendritic polymer with a styrene skeleton and a hydrophilic polymer grafted to a terminal thereof, a temperature-responsive substrate for cell culture having a temperature-responsive surface for cell culture that allows cells to be cultured with high efficiency and which yet allows cultured cells to be exfoliated in a short period of time and with high efficiency by simply changing the temperature of the substrate surface can be prepared conveniently. If this temperature-responsive substrate for cell culture is used, cells obtained from a variety of tissues can be cultured with high efficiency. If this culture method is utilized, cultured cells can be exfoliated intact in a short amount of time with high efficiency. In addition, by using this graft polymer, a wide range of peptides and proteins can also be separated by simply changing the temperature of a chromatographic carrier. This allows for convenient separation procedure and improves the efficiency of separating operations. What is more, the stereoregularity of the dendritic polymer per se may be utilized to enable separation of solutes based on differences in their molecular structures. 1. A temperature-responsive substrate for cell culture comprising a substrate coated with a dendritic polymer with a styrene skeleton and a temperature-sensitive polymer grafted at a terminal thereof.2. The temperature-responsive substrate for cell culture according to claim 1 , which has electric charges at a terminal of the dendritic polymer.3. The temperature-responsive substrate for cell culture according to claim 1 , wherein the polymer having temperature response comprises any one or more of a poly-N-substituted acrylamide derivative claim 1 , a poly-N-substituted methacrylamide derivative claim 1 , a copolymer thereof claim 1 , polyvinyl methyl ether claim 1 , and partially acetylated polyvinyl alcohol claim 1 , or a copolymer thereof with another monomer.4. The temperature- ...

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28-06-2018 дата публикации

LIGAND IMMOBILIZATION METHOD

Номер: US20180179250A1
Принадлежит: KANEKA CORPORATION

A method for immobilizing a ligand on a formyl group-containing insoluble base material includes producing an imine by mixing the ligand and the formyl group-containing insoluble base material, and reducing the imine by using a borane complex, wherein the ligand comprises an amino group and has a specific affinity for a target compound, and wherein the borane complex has a Lewis base ligand having pKof 6.5 or less. 1. A method for immobilizing a ligand on a formyl group-containing insoluble base material , the method comprising:producing an imine by mixing the ligand and the formyl group-containing insoluble base material; andreducing the imine by using a borane complex,wherein the ligand comprises an amino group and has a specific affinity for a target compound, and{'sub': 'a', 'wherein the borane complex has a Lewis base ligand having pKof 6.5 or less.'}2. The method according to claim 1 , wherein the Lewis base ligand is one or more selected from the group consisting of a nitrogen-containing heterocyclic aromatic compound claim 1 , and an aromatic hydrocarbon compound having an amino group as a substituent.3. The method according to claim 1 , wherein the ligand is a peptide.4. The method according to claim 3 , wherein the ligand is an antibody affinity ligand.5. The method according to claim 4 , wherein the antibody affinity ligand is Protein A claim 4 , Protein G claim 4 , Protein L or an analog thereof.6. The method according to claim 1 , wherein the formyl group-containing insoluble base material is at least one selected from the group consisting of a polysaccharide claim 1 , a synthetic polymer and glass.7. The method according to claim 1 , wherein the formyl group-containing insoluble base material is cellulose or agarose.8. The method according to any one of claim 1 , wherein a form of the formyl group-containing insoluble base material is a porous bead claim 1 , a monolith or a porous membrane.9. A method for purifying a target compound claim 1 , ...

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13-06-2019 дата публикации

Guanidine-Functionalized Particles and Methods of Making and Using

Номер: US20190177342A1
Принадлежит:

Guanidine-functionalized particles and methods of making and using such particles. 1. A guanidine-functionalized silica gel particle , comprising:{'sub': n', 'm, 'claim-text': where —O is an oxygen atom that is covalently bonded to the surface of the silica gel particle,', 'n is 1, 2 or 3,', 'S is a spacer group comprising a backbone with m atoms,', 'm is 2-16, inclusive,', {'sub': '2', 'claim-text': 'and wherein the guanidine group is charged and comprises an associated counterion and wherein the counterion does not comprise a halogen.', 'G is a guanidine group of the formula NH—C(NH)—NH,'}], 'a silica gel particle comprising at least one ligand comprising a guanidine group, the ligand comprising the formula —OSi—S-G,'}2. The particle of wherein all m atoms of the backbone of the spacer group S are carbon atoms.3. The particle of wherein m=3.4. The particle of wherein the spacer group S comprises a secondary amine.5. The particle of wherein the guanidine group is the reaction product of a primary amine and O-methylisourea hemisulfate.6. The particle of wherein the silica gel particle comprises a particle size of about 25-100 microns and a pore size of about 60-2000 Angstroms.7. The particle of wherein the ligand is the reaction product of one or more hydroxyl groups of the silica particle with one or more reactive groups of a silane coupling agent moiety of the ligand.8. The particle of wherein the counterion that is associated with the guanidine group is a sulfate ion.9. The particle of wherein the counterion that is associated with the guanidine group is a bisulfate ion.10. The particle of wherein the counterion that is associated with the guanidine group is a hydroxide ion.11. The particle of wherein the guanidine group is the reaction product of a primary amine with O-methylisourea hemisulfate.12. The particle of wherein residual hydroxyl groups are present on the surface of the particle.13. The particle of wherein each ligand has only a single guanidine group. ...

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18-09-2014 дата публикации

Epoxy chemistry derived materials as mixed mode chromatography media, method for their synthesis and use

Номер: US20140273264A1
Принадлежит: Dionex Corp

This invention provides mixed-mode stationary phase compositions, devices and systems comprising the stationary phases as well as methods of producing these compositions using epoxide ring-opening reactions. Also provided are methods of using the stationary phases of the invention in separations.

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20-06-2019 дата публикации

Material for blood purification

Номер: US20190184371A1
Принадлежит: TORAY INDUSTRIES INC

An object of the present invention is to provide a material for blood purification having the capability to remove cytokines and activated leukocyte-activated platelet complexes. The present invention provides a material for blood purification, the material containing a water-insoluble material in which a ligand having an amide group(s) and an amino group(s) is bound to a substrate, wherein the content of the amide group(s) is 3.0 to 7.0 mmol per 1 g dry weight of the water-insoluble material; and wherein the content of the amino group(s) is 1.0 to 7.0 mmol per 1 g dry weight of the water-insoluble material.

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23-07-2015 дата публикации

Ligand grafted substrates

Номер: US20150203645A1
Принадлежит: 3M Innovative Properties Co

Ligand-functionalized substrates are describe that are useful in selectively binding and removing biological materials from biological samples, and methods for preparing the same.

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21-07-2016 дата публикации

Mutated immunoglobulin-binding polypeptides

Номер: US20160207966A1
Принадлежит: GE Healthcare Bio Sciences AB

A polypeptide with improved alkaline stability, which polypeptide comprises a mutant of a B or C domain of Staphylococcus Protein A, as specified by SEQ ID NO 1 or SEQ ID NO 2, or of Protein Z, as specified by SEQ ID NO 3, wherein at least the glutamine residue at position 15 has been mutated to an amino acid other than asparagine. The invention also discloses multimers of the polypeptide, as well as separation matrices comprising the multimers or polypeptides.

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20-07-2017 дата публикации

HIGH EFFICIENCY, ULTRA-STABLE, BONDED HYDROPHILIC INTERACTION CHROMATOGRAPHY (HILIC) MATRIX ON SUPERFICIALLY POROUS PARTICLES (SPPS)

Номер: US20170203234A1
Принадлежит:

The present invention relates to superficially porous particles (SPPs), also called core-shell, porous shell or fused core particles, which are state-of-the-art support materials used in the production of HPLC columns. Hydrolytically stable, highly selective superficially porous particle (SPP) hydrophilic interaction liquid chromatographic (HILIC) stationary phases having higher efficiencies and shorter retention times than analogous stationary phases on fully porous particles (FPP) is provided. 1. Covalently bonded ultra-stable hydrophilic interaction chromatography (HILIC) phases comprising superficially porous particle (SPP) linked to a HILIC selector.2. The covalently bonded ultra-stable hydrophilic interaction chromatography (HILIC) phases of claim 1 , wherein SPP has a particle diameter from about 0.5 microns to about 20 microns.3. The covalently bonded ultra-stable hydrophilic interaction chromatography (HILIC) phases of claim 1 , wherein SPP has a particle diameter from about 1.3 microns to about 10 microns.4. The covalently bonded ultra-stable hydrophilic interaction chromatography (HILIC) phases of claim 1 , wherein SPP has a particle diameter from about 1.7 microns to about 5.0 microns.5. The covalently bonded ultra-stable hydrophilic interaction chromatography (HILIC) phases of claim 1 , wherein SPP has a particle diameter selected from the group consisting of about 1.7 claim 1 , about 2.7 and about 4.0 microns.6. (canceled)7. (canceled)8. (canceled)9. The covalently bonded ultra-stable hydrophilic interaction chromatography (HILIC) phases of claim 1 , wherein the SPP has a pore size from about 100 angstroms to about 300 angstroms.10. (canceled)11. (canceled)12. The covalently bonded ultra-stable hydrophilic interaction chromatography (HILIC) phases of claim 1 , wherein the SPP has a pore size of about 120 angstroms.13. The covalently bonded ultra-stable hydrophilic interaction chromatography (HILIC) phases of claim 1 , wherein the SPP has a surface area ...

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05-08-2021 дата публикации

Superficially porous materials comprising a substantially nonporous core having narrow particle size distribution; process for the preparation thereof; and use thereof for chromatographic separations

Номер: US20210237033A1
Принадлежит: Waters Technologies Corp

Novel chromatographic materials for chromatographic separations, columns, kits, and methods for preparation and separations with a superficially porous material comprising a substantially nonporous core and one or more layers of a porous shell material surrounding the core. The material of the invention is comprised of superficially porous particles and a narrow particle size distrution. The material of the invention is comprised of a superficially porous monolith, the substantially nonporous core material is silica; silica coated with an inorganic/organic hybrid surrounding materia; a magnetic core material; a magnetic core material coated with silica; a high thermal conductivity core material; a high thermal conductivity core material coated with silica; a composite material; an inorganic/organic hybrid surrounding material; a composite material coated with silica; a magnetic core material coated with an inorganic/organic hybrid surrounding material; or a high thermal conductivity core material coated with an inorganic/organic hybrid surrounding material.

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26-07-2018 дата публикации

Protein Separations Using An Acrylamide Containing Filter

Номер: US20180208624A1
Принадлежит: EMD Millipore Corp

Novel compositions for removing impurities such as, protein aggregates, from a sample containing a protein of interest, e.g., an antibody. Such compositions can be used prior to the virus filtration step during protein purification, to remove aggregates and protect the virus filter from fouling, therefore improving virus filter capacity. A porous solid support including a co-polymer having at least two monomers, wherein at least one of the monomers comprises acrylamide and at least a second monomer comprises a hydrophobic binding group, where the solid support selectively binds protein aggregates, thereby to separate the monomeric protein of interest from the protein aggregates. The method can be performed under neutral to high pH and high conductivity conditions.

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05-08-2021 дата публикации

PACKING MATERIAL FOR ION CHROMATOGRAPHY AND PRODUCTION METHOD THEREFOR

Номер: US20210237034A1
Принадлежит: SHOWA DENKO K.K.

A packing material for ion chromatography has a structure in which a polyethyleneimine is bonded, directly or through a spacer, to a surface of an organic porous substrate constituted of a hydroxylated crosslinked copolymer, and a functional group represented by formula (1) 2. The packing material for ion chromatography according to claim 1 , wherein R is a 2-hydroxy propylene group claim 1 , and at least one of R claim 1 , Rand Ris a C1 to C10 alkyl group having an amino group.4. The packing material for ion chromatography according to claim 1 , wherein a polyethyleneimine is bonded through a spacer to a crosslinked copolymer.5. The packing material for ion chromatography according to claim 4 , wherein a crosslinked polymer has a hydroxyl group claim 4 , and the spacer has a structure derived from a multifunctional glycidyl ether or epichlorohydrin.6. The packing material for ion chromatography according to claim 5 , wherein the spacer is a multifunctional glycidyl ether claim 5 , and the multifunctional glycidyl ether is selected from 1 claim 5 ,4-butanediol diglycidyl ether claim 5 , ethylene glycol diglycidyl ether claim 5 , polyethylene glycol diglycidyl ether claim 5 , and glycerol diglycidyl ether.7. The packing material for ion chromatography according to claim 6 , wherein the multifunctional glycidyl ether is 1 claim 6 ,4-butanediol diglycidyl ether.8. The packing material for ion chromatography according to claim 1 , wherein the crosslinked copolymer is a crosslinked polyvinyl alcohol polymer.9. A production method of the packing material for ion chromatography according to claim 1 , comprising a step of bonding claim 1 , directly or through a spacer claim 1 , a polyethyleneimine to the surface of an organic porous substrate constituted of a crosslinked copolymer (step 1) claim 1 , a step of reacting a nitrogen atom contained in the polyethyleneimine with a multifunctional glycidyl ether (step 2) claim 1 , and a step of reacting a tertiary amine with the ...

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03-08-2017 дата публикации

Guanidine-Functionalized Particles and Methods of Making and Using

Номер: US20170217995A1
Принадлежит:

Guanidine-functionalized particles and methods of making and using such particles. 1. A method of making a guanidine-functionalized particle , comprising: [{'br': None, 'sub': n', '3-n', 'm, 'sup': 'a', '(RO)RSi—S—X'}, 'where RO is an alkoxy group comprising one or two carbons, or is an acetoxy group,', 'where n is 1, 2 or 3,', {'sup': 'a', 'where Ris an unreactive group,'}, 'where S is a spacer group comprising a backbone with m atoms,', 'm is from 2-16, inclusive, and', 'where X is a primary amine that is capable of reacting with the O-methylisourea to form a guanidine group;, 'reacting O-methylisourea hemisulfate with a linker molecule comprising the formula'}and,reacting at least one of the RO groups of the linker molecule with a hydroxyl group of the particle to form a covalent bond between the linker molecule and the particle.2. The method of wherein the (RO)Si moiety comprises a trimethoxysilane moiety.3. The method of wherein the linker molecule is 3-aminopropyltrimethoxysilane.4. The method of wherein the (RO)Si moiety comprises a triethoxysilane moiety.5. The method of wherein all m atoms of the backbone of the spacer group S are carbon atoms.6. The method of wherein m=3.7. The method of wherein the spacer group S comprises at least one hetero atom.8. The method of wherein the spacer group S comprises at least one secondary amine.9. The method of wherein the linker molecule is N-(2-aminoethyl)-3-aminopropyltrimethoxysilane.10. The method of wherein the step of reacting at least one of the RO groups of the linker molecule with a hydroxyl group of the particle to form a covalent bond between the linker molecule and the particle claim 1 , is performed after the reacting of the O-methylisourea hemisulfate with the linker molecule.11. The method of wherein the step of reacting at least one of the RO groups of the linker molecule with a hydroxyl group of the particle to form a covalent bond between the linker molecule and the particle claim 1 , is performed ...

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03-08-2017 дата публикации

Immobilisation of Chelating Groups for Immobilised Metal Ion Chromatography (IMAC)

Номер: US20170218013A1

The present invention refers to a method for binding a polycarboxylic acid to a solid phase. Further, the invention refers to a solid phase having a polycarboxylic acid immobilized thereto and methods of using the solid phase, e.g. for purifying His-tagged recombinant polypeptides. 1. A method for immobilized metal ion chromatography (IMAC) , comprising contacting a sample with an immobilized chelator having 6 or more coordination groups.2. The method according to wherein the immobilized chelator is a polycarboxylic acid amide or ester having 6 or more coordination groups.3. The method according to claim 2 , wherein said coordination groups are selected from the group consisting of amino claim 2 , carboxyl claim 2 , carboxamide and hydroxamate groups.5. The method according to claim 4 , wherein said PCA is the residue of an amino polycarboxylic acid or a salt thereof.6. The method according to claim 5 , wherein the polycarboxylic acid is selected from the group consisting of ethylene diamino tetraacetic acid (EDTA) claim 5 , ethylene glycol-bis(2-aminoethylether)-N claim 5 ,N claim 5 ,N′ claim 5 ,N′-tetraacetic acid (EGTA) claim 5 , diethylene triamino pentaacetic acid (D PTA) claim 5 , triethylene tetramine-N claim 5 , N claim 5 , N′ claim 5 ,N′ claim 5 ,N″ claim 5 ,N″-hexa-acetic acid (TTHA) claim 5 , and salts thereof.7. The method according to claim 6 , wherein said polycarboxylic acid is ethylene diamino tetraacetic acid (EDTA).9. The method of claim 1 , wherein the chelator is complexed with a metal ion.10. The method according to claim 9 , wherein said metal ion is a transition metal ion.11. The method according to claim 10 , wherein said transition metal is a Ni ion.12. A method for binding a polycarboxylic acid having 6 or more coordination groups to a solid phase claim 10 , comprising the steps:(a) providing a polycarboxylic acid and a solid phase comprising amino groups,(b) reacting the amino groups with the polycarboxylic acid in the presence of a ...

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09-08-2018 дата публикации

Novel Chelator and Use Thereof

Номер: US20180223003A1
Принадлежит:

The present invention relates to dimeric pentadentate chelators with exceptionally strong binding of metal ions, for detection, immobilization and purification of biomolecules. Dimeric chelators offer a cooperativity of binding of two adjacent immobilized metal ions simultaneously to a histidine-tagged biomolecule, which gives advantageous properties regarding strength of binding compared to a corresponding monomer chelator. In addition, a dimer increases the selectivity (ease of separation) against non-tagged biomolecules with low metal-ion affinity. 2. The dimeric pentadentate chelator of claim 1 , wherein Q is a solid phase comprising a natural or synthetic polymer.3. The dimeric pentadentate chelator of claim 2 , wherein the solid phase is a porous chromatographic support.4. The dimeric pentadentate chelator of claim 2 , wherein Q is made of a cross-linked carbohydrate material.5. The dimeric pentadentate chelator of claim 4 , wherein the cross-linked carbohydrate material is agarose claim 4 , agar claim 4 , cellulose claim 4 , dextran claim 4 , chitosan claim 4 , konjac claim 4 , carrageenan claim 4 , gellan claim 4 , or alginate.6. The dimeric pentadentate chelator of claim 4 , wherein the cross-linked carbohydrate material is agarose.7. The dimeric pentadentate chelator of claim 2 , wherein Q is made of synthetic polymers such as styrene derivatives claim 2 , divinylbenzene claim 2 , acryl amides claim 2 , acrylate esters claim 2 , methacrylate esters claim 2 , vinyl esters or vinyl amides.8. The dimeric pentadentate chelator of claim 7 , wherein the synthetic polymers comprise styrene derivatives claim 7 , divinylbenzene claim 7 , acryl amides claim 7 , acrylate esters claim 7 , methacrylate esters claim 7 , vinyl esters claim 7 , vinyl amides claim 7 , or a combination thereof.9. The dimeric pentadentate chelator of claim 2 , wherein Q comprises magnetic particles.10. The dimeric pentadentate chelator of claim 1 , wherein Q is a solid phase comprising a ...

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18-07-2019 дата публикации

CHROMATOGRAPHIC MATERIALS

Номер: US20190217273A1
Принадлежит: WATERS TECHNOLOGIES CORPORATION

In one aspect, the present invention provides a chromatographic stationary phase material for various different modes of chromatography represented by Formula 1: [X](W)(Q)(T)(Formula 1). X can be a high purity chromatographic core composition having a surface comprising a silica core material, metal oxide core material, an inorganic-organic hybrid material or a group of block copolymers thereof. W can be absent and/or can include hydrogen and/or can include a hydroxyl on the surface of X. Q can be a functional group that minimizes retention variation over time (drift) under chromatographic conditions utilizing low water concentrations. T can include one or more hydrophilic, polar, ionizable, and/or charged functional groups that chromatographically interact with the analyte. Additionally, b and c can be positive numbers, with the ratio 0.05≤(b/c)≤100, and a≥0. 262-. (canceled)63. The chromatographic stationary phase material of claim 1 , wherein the chromatographic stationary phase material is in the form of a plurality of particles.64. The chromatographic stationary phase material of claim 1 , wherein the chromatographic stationary phase material is in the form of a monolith.65. The chromatographic stationary phase material of claim 1 , wherein the chromatographic stationary phase material is in the form of a superficially porous material.66. The chromatographic stationary phase material of claim 1 , wherein the chromatographic stationary phase material has chromatographically enhancing pore geometry.67. The chromatographic stationary phase material of claim 63 , wherein the plurality of particles have sizes between about 1.5 and 5 microns.68. The chromatographic stationary phase material of claim 1 , wherein the chromatographic stationary phase material has a surface area of about 25 to 1100 m/g.69. The chromatographic stationary phase material of claim 1 , wherein the chromatographic stationary phase material has a pore volume of about 0.2 to 2.0 cm/g.70. The ...

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09-07-2020 дата публикации

METHOD FOR PREPARING A MONOLITHIC STATIONARY PHASE, ASSOCIATED METHOD FOR PRODUCING A CHROMATOGRAPHY COLUMN AND ASSOCIATED SEPARATION METHOD

Номер: US20200215514A1

The invention relates to a method for preparing a monolithic stationary phase in the interior volume of a chromatography column made of thermoplastic polymer. This method comprises the following steps: (i) modifying the inner wall of the chromatography column by implementing the following steps: (a) preparing a polymerizable anchoring composition comprising at least one particular methacrylate monomer, one or more solvents and 2,2-dimethoxy-2-phenylacetophenone, (b) depositing, on the inner wall of the column, the polymerizable anchoring composition prepared in step (a), and (c) polymerizing the polymerizable anchoring composition by irradiation with ultraviolet radiation; (ii) introducing, into the interior volume of the column, a polymerizable monolith synthesis composition comprising first and second particular (meth)acrylate monomers, one or more pore-forming agents and a free-radical polymerization initiator; and (iii) polymerizing the polymerizable monolith synthesis composition. The invention also relates to a method for producing a chromatography column comprising such a monolithic stationary phase and to a chromatographic separation method using such a column. 116-. (canceled)17. A method for producing a chromatography column , the method comprising: [ [ at least one (meth)acrylate monomer selected from the group consisting of ethylene glycol dimethacrylate, 1,4-butanediol diacrylate, triethylene glycol dimethacrylate, and trimethylolpropane trimethacrylate,', 'one or more solvents, and', '2,2-dimethoxy-2-phenylacetophenone,, '(a) preparing a polymerizable anchoring composition comprising, '(b) depositing, on the inner wall of the chromatography column, the polymerizable anchoring composition prepared at step (a), and', '(c) polymerizing the polymerizable anchoring composition via ultraviolet radiation;, '(i) modifying the inner wall of the chromatography column by implementing the following successive steps (a) to (c), a first (meth)acrylate monomer ...

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17-08-2017 дата публикации

ANIONIC EXCHANGE-HYDROPHOBIC MIXED MODE

Номер: US20170232433A1
Автор: Frost Russell, Liao Jiali
Принадлежит:

Anion exchange-hydrophobic mixed mode ligands and methods of their use are provided. 1. A chromatographic solid support linked to a ligand having the formula:{'sup': +', '1', '2', '3, 'Support-(X)—N(R, R)-R-L—Ar, wherein the positively-charged nitrogen is in salt form, and wherein'}X is a spacer or absent;{'sup': 1', '2, 'Rand Rare each selected from hydrogen and an alkyl comprising 1-6 carbons;'}{'sup': '3', 'Ris an alkyl comprising 1-6 carbons or a cyclo alkyl comprising 1-6 carbons;'}{'sup': 4', '4, 'L is NR, O, or S; wherein Ris hydrogen or an alkyl comprising 1-6 carbons; and'}Ar is an aryl.2. The chromatographic solid support of claim 1 , wherein Rand Rare hydrogen.3. The chromatographic solid support of claim 1 , wherein Ris an alkyl comprising 1-4 carbons.4. The chromatographic solid support of claim 1 , wherein Ris an alkyl comprising 2 carbons.5. The chromatographic solid support of claim 1 , wherein the aryl is a phenyl.6. The chromatographic solid support of claim 1 , wherein the aryl is a substituted phenyl.7. The chromatographic solid support of claim 6 , wherein the substituted phenyl is an alkyl-substituted phenyl.8. The chromatographic solid support of claim 1 , wherein Rand/or Rare an alkyl comprising 1-6 carbons and Ar is an alkyl-substituted phenyl.9. The chromatographic solid support of claim 1 , wherein the ligand is N-phenylethylenediamine or a salt thereof.10. The chromatographic solid support of claim 1 , wherein the ligand is 2-phenoxyethylamine or a salt thereof.11. The chromatographic solid support of claim 1 , wherein X is absent.12. The chromatographic solid support of claim 1 , wherein X is a spacer. The present application is a divisional of U.S. application Ser. No. 13/785,632, filed Mar. 5, 2013, which claims benefit of priority to U.S. Provisional Patent Application No. 61/608,418, filed Mar. 8, 2012, which is incorporated by reference for all purposes.The extraction of immunoglobulins from source liquids, which are primarily ...

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03-09-2015 дата публикации

FUNCTIONALIZED SILICEOUS FILTERS FOR SAMPLING AND PURIFICATION OF ORGANIC COMPOUNDS

Номер: US20150246339A1
Принадлежит: CONSIGLIO NAZIONALE DELLE RICERCHE

The invention relates to filtering systems comprising filters consisting of fibers of silanized siliceous material for environmental sampling, in particular of pollutants. 1. Filtering system comprising filters consisting of fibers of siliceous material silanized with the (Si—O)nSiRm group wherein —(Si—O)— is the fraction of functionalized surface and R , equal or different , is hydrogen or a moiety comprising at least one halogenated or non-halogenated alkyl and/or at least one halogenated or non-halogenated alkene and/or at least one halogenated or non-halogenated aromatic ring and/or at least one halogenated or non-halogenated alcoholic group and/or at least one nitrile and/or at least one ammine group and/or at least one carbonyl group , and n and m are integers wherein n+m=4 , n>0 , m>0.2. The filtering system of wherein the filters are selected from the group consisting of: quartz fiber filters claim 1 , glass fiber filters and filters of sintered silica.3. The filtering system of wherein the filters have a percentage of retention of the powders with diameter greater than 0.3 μm higher than 80%.4. The filtering system of wherein the filters have a thickness in the range between 0.01 and 50 mm.5. The filtering system of wherein the filters have an area from 0.1 cmto 2500 cm.6. The filtering system of wherein R claim 1 , equal or different claim 1 , is selected from the group consisting of: hydrogen claim 1 , linear claim 1 , branched claim 1 , cyclic and polycyclic alkanes claim 1 , cumulative conjugated and unconjugated alkenes claim 1 , cumulative conjugated and unconjugated polyenes claim 1 , aromatic rings claim 1 , polyaromatic rings claim 1 , alkyl vinyl alkynyl aryl acyl halides claim 1 , primary secondary tertiary and cyclic non-cyclic aromatic non-aromatic amines and their salts claim 1 , alkylammonium salts claim 1 , haloamines claim 1 , primary secondary tertiary amides and their salts claim 1 , lactams claim 1 , nitriles claim 1 , alcohols ...

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25-08-2016 дата публикации

SYSTEM AND METHOD FOR REMOVING TRANSITION METALS FROM SOLUTION

Номер: US20160243463A1
Принадлежит:

A metal sequestering material can be contacted with a reaction mixture of a metal-catalyzed reaction to remove transition metals or transition metal complexes. The reaction mixture contains transition metals and a reaction product in solution. These transition metals may be, for example, Pd, Ir, Ru, Rh, Pt, Au, or Hg. The concentration of transition metals in the reaction mixture is reduced to less than 100 ppm or even less than 10 ppm. 1. A method for removing transition metals or transition metal complexes from a reaction mixture comprising:a) providing a reaction mixture of a metal-catalyzed reaction, the reaction mixture comprising transition metals and a reaction product in solution, wherein the transition metals are selected from the group consisting of a Group 8 element, a Group 9 element, a Group 10 element, a Group 11 element, and a Group 12 element; i) a support;', 'ii) a linker bound to the support; and', 'iii) at least one isocyanide bound to the linker; and, 'b) contacting a metal sequestering material with the reaction mixture, wherein the metal sequestering material comprisesc) separating the metal sequestering material from the reaction mixture,wherein a concentration of the transition metals in the reaction mixture after the separation of the metal sequestering material is reduced to less than 100 ppm.2. The method of claim 1 , wherein the transition metals are selected from the group consisting of Pd claim 1 , Ir claim 1 , Ru claim 1 , Rh claim 1 , and Pt.3. The method of claim 1 , wherein the transition metals are Au or Hg.4. The method of claim 1 , wherein at least some of the transition metals are bound to the isocyanide before the separation of the metal sequestering material.5. The method of claim 1 , wherein the contacting is performed such that the concentration of the transition metals is reduced to less than 10 ppm.6. The method of claim 1 , wherein greater than 97% of the transition metals are bound to the metal sequestering material ...

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23-07-2020 дата публикации

LIGAND BOUND MBP MEMBRANES, USES AND METHOD OF MANUFACTURING

Номер: US20200232978A1
Принадлежит: TeraPore Technologies, Inc.

Compositions and methods are described for self-assembled polymer materials having at least one of macro, meso, or micro pores. 1. A self-assembled polymer material containing at least one of macro , meso , or micro pores , at least some of which are isoporous , comprising at least one multi-block polymer (MBP) , at least two of the polymer blocks are chemically distinct , at least one of said chemically distinct blocks is modified to include a covalent or noncovalent moiety link using a linker , and an affinity ligand bound to said linker.2. The material of claim 1 , wherein the material is one of asymmetric or symmetric.3. The material of claim 1 , wherein the material comprises macroporous domains and mesoporous wall structures in a single claim 1 , integral scalable structure.4. The material of claim 2 , wherein the material comprises continuous macroporous domains.5. The material of claim 4 , wherein the material is asymmetric and has mesopores and macropores.6. The material of claim 1 , wherein the MBP includesa. more than one affinity ligand or more than one linker, orb. an affinity ligand or linker containing more than one functionality, orc. an affinity ligand or linker located in part or completely on more than one polymer block.7. A method of preparing the material of claim 1 , comprising claim 1 ,a. modifying a surface of an MBP with an affinity ligand by non-covalent attachment; or,b. modifying the MBP with a linker that provides functionality for the subsequent attachment of an affinity ligand; or,c. varying the amount of the MBP modified with a linker or affinity ligand relative to the stoichiometry of the MBP, comprising varying the time, temperature, and concentration of modifier, to modify 10-100% of available sites; or,d. conformally coating a linking material by covalent or non-covalent moieties to a surface of the material to provide an integral, but discrete physical layer of the linker or affinity ligand; or,e. providing the material with ...

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30-08-2018 дата публикации

Adsorption Medium, Method for Production Thereof, and Use Thereof for Purification of Biomolecules

Номер: US20180243724A1
Принадлежит:

The present invention relates to an adsorption medium, especially a chromatography medium, to a method for the production thereof, and to the use of the adsorption medium according to the invention or of an adsorption medium produced according to the invention for the purification of biomolecules. 1. An adsorption medium , especially a chromatography medium comprising a chromatic matrix;polymeric space elements which have been bonded to the surface of the chromatography matrix; andPolymer chains containing chromatographically active centers, wherein the polymer chains have been bonded to the polymeric spacer elements.2. The adsorption medium as claimed in wherein the chromatography matrix comprising a material selected from the group consisting of natural or synthetic fibers claim 1 , (polymer) membranes claim 1 , porous claim 1 , polymeric monolithic shaped bodies claim 1 , polymer gels claim 1 , films claim 1 , nonwovens claim 1 , wovens and inorganic materials.3. The adsorption medium as claimed in claim 1 , wherein the polymeric spacer elements are selected from the group consisting of polyamines claim 1 , polyalcohols claim 1 , polythiols claim 1 , poly(meth)acrylates claim 1 , poly(metho)acrylamides claim 1 , poly-N-alkyl(meth)acrylamides and also copolymers consisting of two or more of the above polymers claim 1 , and copolymers consisting of one or more of the above polymers and of polymers which do not bear nucleophilic fuctional groups.4. The adsorption medium as claimed in claim 3 , wherein the polymeric spacer elements are polyamines.5. The adsorption medium as claimed in claim 1 , wherein the polymeric spacer elements do not have epoxy groups.6. The adsorption medium as claimed in claim 1 , wherein the adsorption medium has a degree of grafting from 1% to 50%.7. The adsorption medium as claimed in claim 1 , wherein the functional group density of the chromatography matrix is from 1.5 to 30 nm.8. The adsorption medium as claimed in claim 1 , wherein the ...

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30-08-2018 дата публикации

MUTATED IMMUNOGLOBULIN-BINDING POLYPEPTIDES

Номер: US20180244729A1
Принадлежит: GE Healthcare BioProcess R&D AB

The invention discloses a polypeptide with improved alkaline stability, which polypeptide comprises a mutant of a B or C domain of Staphylococcus Protein A (SpA), as specified by SEQ ID NO 1 or SEQ ID NO 2, or of Protein Z, as specified by SEQ ID NO 3, wherein at least the glutamine residue at position 9 has been mutated to an amino acid other than asparagine. The invention also discloses multimers of said polypeptide, as well as separation matrices comprising the multimers or polypeptides. 1. A immunoglobulin-binding polypeptide with improved alkaline stability , which polypeptide comprises a mutant of the B-domain or C-domain of Staphylococcus Protein A (SpA) , as specified by SEQ ID NO 1 or SEQ ID NO 2 , or of Protein Z , as specified by SEQ ID NO 3 , or of Zvar , as specified by SEQ ID NO 4 , wherein at least the glutamine residue at position 9 has been mutated to an amino acid other than asparagine.2. The polypeptide of claim 1 , wherein the glutamine residue at position 9 has been mutated to an alanine.3. The polypeptide of claim 1 , wherein at least the amino acid at position 3 has been mutated to an amino acid other than asparagine claim 1 , proline claim 1 , or cysteine claim 1 , or wherein the amino acid residue at position 3 is an alanine.4. The polypeptide of claim 1 , wherein at least the amino acid at position 6 has been mutated to an amino acid other than asparagine claim 1 , proline claim 1 , or cysteine claim 1 , or wherein the amino acid residue at position 6 is an aspartic acid.5. The polypeptide of claim 1 , wherein at least the glutamine at position 10 has been mutated to an amino acid other than asparagine claim 1 , proline claim 1 , or cysteine claim 1 , or wherein the amino acid residue at position 10 is a glutamine.6. The polypeptide of claim 1 , wherein at least the glutamic acid at position 15 has been mutated to an amino acid other than asparagine claim 1 , proline claim 1 , or cysteine claim 1 , or wherein the amino acid residue at ...

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31-08-2017 дата публикации

AFFINITY CHROMATOGRAPHY MATRIX

Номер: US20170247407A1
Принадлежит: GE Healthcare BioProcess R&D AB

The invention discloses a polypeptide capable of binding immunoglobulins or immunoglobulin-containing proteins, which polypeptide comprises six or more domains of protein Z or the C domain of protein A or a functional variant thereof. It also discloses separation matrices comprising the polypeptide and methods of using the separation matrices for separation of immunoglobulins or immunoglobulin-containing proteins. 1. A separation matrix comprising a plurality of chromatography ligands coupled to a solid support ,wherein the ligand comprises one or more mutated Domain C of Staphylococcus protein A (SpA) and having a sequence that is at least 80% identical to the amino acid sequence shown in SEQ ID NO:1 or at least 77% identical to the amino acid sequence shown in SEQ ID NO:2.2. The separation matrix of claim 1 , wherein the ligands after 5 hours incubation in 0.5 M NaOH has retained at least 95% of its original binding capacity.3. The separation matrix of claim 1 , wherein the ligand is capable of binding to the Fab part of an antibody.4. The separation matrix of claim 1 , wherein the ligand comprises one or more mutated Domain C of Staphylococcus protein A (SpA) and having a sequence that is at least 95% identical to the amino acid sequence shown in SEQ ID NO:1.5. The separation matrix of claim 1 , wherein the ligand comprises one or more mutated Domain C of Staphylococcus protein A (SpA) and having a sequence that is at least 94% identical to the amino acid sequence shown in SEQ ID NO: 2.6. The separation matrix of claim 1 , wherein the ligand comprises one or more mutated Domain C of Staphylococcus protein A (SpA) and having a sequence that is at least 98% identical to the amino acid sequence shown in SEQ ID NO:1 or SEQ ID NO: 2.7. The separation matrix of claim 1 , wherein the one or more mutated Domain C of Staphylococcus protein A (SpA) comprises a sequence selected from SEQ ID NO: 1 claim 1 , SEQ ID NO: 2 claim 1 , SEQ ID NO: 1 with mutation G29A claim 1 , and ...

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30-07-2020 дата публикации

Fc binding proteins with cysteine in the c-terminal helical region

Номер: US20200238197A1
Принадлежит: Repligen Corp

The present invention relates to Fc binding proteins comprising one or more domains with Cysteine in the C-terminal helical region. The invention further relates to affinity matrices comprising the Fc binding proteins of the invention. The invention also relates to a use of these Fc binding proteins or affinity matrices for affinity purification of immunoglobulins and to methods of affinity purification using the Fc binding proteins of the invention.

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30-07-2020 дата публикации

ADSORBENT FOR CALCIPROTEIN PARTICLES, ADSORPTION REMOVAL SYSTEM, AND METHOD FOR UTILIZATION THEREOF

Номер: US20200238253A1
Принадлежит:

The purpose of the present invention is to adsorb calciprotein particles. An adsorbent for calciprotein particles of the present invention is characterized in that the surface of a water-insoluble carrier is covalently bonded, through a hydrocarbon group, to at least one selected from the group consisting of amino group, carboxyl group, phosphate group, phosphono group, phosphino group, and thiol group. 1. An adsorbent for calciprotein particles , comprising a water-insoluble carrier , whereina surface of the water-insoluble carrier is covalently bonded, through a hydrocarbon group, to at least one group selected from the group consisting of an amino group, carboxyl group, phosphate group, phosphono group, phosphino group, and thiol group.2. The adsorbent according to claim 1 , wherein the hydrocarbon group is a linear hydrocarbon group.3. The adsorbent according to claim 1 , wherein the hydrocarbon group is covalently bonded to two or more of the phosphono groups.4. The adsorbent according to claim 1 , wherein two of the phosphono groups and a hydroxyl group are covalently bonded to a terminal carbon atom of the hydrocarbon group claim 1 , and the hydrocarbon group is a linear propyl group claim 1 , a linear butyl group claim 1 , or a linear hexyl group.5. The adsorbent according to claim 1 , wherein one of the phosphono groups is covalently bonded to a terminal carbon atom of the hydrocarbon group claim 1 , and the hydrocarbon group is an undecyl group.6. The adsorbent according to claim 1 , wherein the carrier is porous.7. The adsorbent according claim 1 , which adsorbs calciprotein particles in body fluid.8. An adsorber of calciprotein particles claim 1 , wherein the adsorber comprises a container having a liquid inlet and a liquid outlet claim 1 , and the container is packed with the adsorbent according to .9. A system of adsorbing calciprotein particles claim 8 , comprising the adsorber according to and a pump for supplying liquid to the adsorber claim 8 , and ...

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23-09-2021 дата публикации

CHROMATOGRAPHY LIGAND COMPRISING DOMAIN C FROM STAPHYLOCOCCUS AUREUS PROTEIN A FOR ANTIBODY ISOLATION

Номер: US20210291143A1
Принадлежит:

The present invention relates to a chromatography ligand, which comprises Domain C from protein A (SpA), or a functional fragment or variant thereof. The chromatography ligand presents an advantageous capability of withstanding harsh cleaning in place (CIF) conditions, and is capable of binding Fab fragments of antibodies. The ligand may be provided with a terminal coupling group, such as arginine or cysteine, to facilitate its coupling to an insoluble carrier such as beads or a membrane. The invention also relates process of using the ligand in isolation of antibodies, and to a purification protocol which may include washing steps and/or regeneration with alkali. 1. A separation matrix comprising a plurality of chromatography ligands coupled to a solid support ,{'i': 'Staphylococcus', 'wherein the ligand comprises one or more mutated Domain C of protein A (SpA) and having a sequence that is at least 80% identical to the amino acid sequence shown in SEQ ID NO:1 or at least 77% identical to the amino acid sequence shown in SEQ ID NO:2.'}2. The separation matrix of claim 1 , wherein the ligands after 5 hours incubation in 0.5 M NaOH has retained at least 95% of its original binding capacity.3. The separation matrix of claim 1 , wherein the ligand is capable of binding to the Fab part of an antibody.4Staphylococcus. The separation matrix of claim 1 , wherein the ligand comprises one or more mutated Domain C of protein A (SpA) and having a sequence that is at least 95% identical to the amino acid sequence shown in SEQ ID NO:1.5Staphylococcus. The separation matrix of claim 1 , wherein the ligand comprises one or more mutated Domain C of protein A (SpA) and having a sequence that is at least 94% identical to the amino acid sequence shown in SEQ ID NO: 2.6Staphylococcus. The separation matrix of claim 1 , wherein the ligand comprises one or more mutated Domain C of protein A (SpA) and having a sequence that is at least 98% identical to the amino acid sequence shown in SEQ ...

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27-11-2014 дата публикации

BIOSEPARATION COMPOSITIONS AND METHODS FOR MAKING AND USING SAME

Номер: US20140346113A1
Принадлежит:

A composition for use in bioseparation. The composition includes a plurality of hollow particles having a siliceous surface. The composition further includes a surface-modifying agent bonded to the hollow particles. The surface-modifying agent includes a binding segment and a reactive segment. The binding segment includes a silyl group and the reactive segment includes a reactive nitrogen group. 1. A composition for use in bioseparation , the composition comprising:a plurality of hollow particles, the hollow particles comprising a siliceous surface; anda surface-modifying agent bonded to the hollow particles, wherein the surface-modifying agent comprises a binding segment and a reactive segment, wherein the binding segment comprises a silyl group, and wherein the reactive segment comprises a reactive nitrogen group;wherein the plurality of hollow particles have an average density between about 0.05 and 0.4 g/ml.2. The composition according to claim 1 , wherein the hollow particles comprise glass bubbles.3. The composition according to claim 1 , wherein a size distribution of the plurality of hollow particles has a span of less than 1.0.4. The composition of claim 1 , wherein a mean particle size of the plurality of hollow particles ranges from about 10 micrometers to about 100 micrometers.5. The composition of claim 1 , wherein the binding segment has a formula:{'br': None, 'sup': 1', '2, 'sub': 3-x', 'x, '—Si(R)(R);'}wherein x=0, 1, or 2;{'sup': 1', '−, 'wherein each group Rcomprises independently OH or a hydrolyzable group from among halo, alkoxy, aryloxy, aralkyoxy, and acyloxy; and'}{'sup': '2', 'wherein each group Rcomprises independently a non-hydrolyzable group from among alkyl, aryl, and aralkyl.'}6. The composition of claim 1 , wherein the surface-modifying agent further comprises a linking segment claim 1 , the linking segment comprising alkylene claim 1 , arylene claim 1 , or both claim 1 , and optionally further comprising —NH— or alkyleneoxy claim 1 , ...

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15-08-2019 дата публикации

ADSORPTIVE MEMBRANES FOR TRAPPING VIRUSES

Номер: US20190249150A1
Автор: Etzel Mark R.
Принадлежит: WISCONSIN ALUMNI RESEARCH FOUNDATION

A disposable, virus-trapping membrane, and a corresponding method to remove viruses from solution are described. The membrane includes a disposable, micro-porous filter membrane and a ligand immobilized on the membrane. The ligand irreversibly and selectively binds viruses. The ligand also has a pKa sufficiently high to repel antibodies via electrostatic charge repulsion. 122-. (canceled)23. A method of removing viruses from a solution suspected of containing viruses , the method comprising contacting the solution with a disposable , virus-trapping membrane for a time sufficient to a yield log-reduction value (LRV) of at least 1.0 for viruses disposed in the solution , wherein the virus-trapping membrane comprises:a micro-porous filter membrane; anda multi-modal anion-exchange ligand that has a pKa sufficiently high to repel basic proteins via electrostatic charge repulsion immobilized on the filter membrane, wherein the ligand comprises one or more of tyrosinol, tryptophanol, octopamine, 1,3-diamino-2-hydroxypropane, tris(2-aminoethyl)amine, and agmatine.24. The method of claim 23 , wherein the solution comprises salt.25. The method of claim 23 , wherein the ligand comprises one or more of tyrosinol claim 23 , tryptophanol claim 23 , tris(2-aminoethyl)amine claim 23 , and agmatine.26. The method of claim 25 , wherein the solution comprises salt.27. The method of claim 25 , wherein the solution comprises from greater than 0 mM to about 50 mM salt.28. The method of claim 23 , wherein the ligand comprises tris(2-aminoethyl)amine.29. The method of claim 28 , wherein the solution comprises salt.30. The method of claim 29 , wherein the solution is contacted with the virus-trapping membrane for a time sufficient to a yield log-reduction value (LRV) of at least 5.0 for viruses disposed in the solution.31. The method of claim 28 , wherein the solution comprises from greater than 0 mM to about 50 mM salt.32. The method of claim 31 , wherein the solution is contacted with the ...

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14-09-2017 дата публикации

Chromatography Ligand Comprising Domain C From Staphylococcus Aureus Protein A For Antibody Isolation

Номер: US20170259244A1
Принадлежит: GE Healthcare BioProcess R&D AB

The present invention relates to a chromatography ligand, which comprises Domain C from Staphylococcus protein A (SpA), or a functional fragment or variant thereof. The chromatography ligand presents an advantageous capability of withstanding harsh cleaning in place (CIF) conditions, and is capable of binding Fab fragments of antibodies. The ligand may be provided with a terminal coupling group, such as arginine or cysteine, to facilitate its coupling to an insoluble carrier such as beads or a membrane. The invention also relates process of using the ligand in isolation of antibodies, and to a purification protocol which may include washing steps and/or regeneration with alkali.

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13-09-2018 дата публикации

IMMUNOADSORBENT FOR PURIFYING FIVE KINDS OF MYCOTOXINS INCLUDING FUMONISIN B1 AND AFLATOXIN B1, AND COMPLEX AFFINITY COLUMN

Номер: US20180259526A1

The invention relates to an immunoadsorbent for purifying five kinds of mycotoxins including fumonisin Band aflatoxin B, and a complex affinity column. The immunoadsorbent comprises a solid-phase support, and an anti-fumonisin Bmonoclonal antibody, an anti-aflatoxin Bmonoclonal antibody, an anti-ochratoxin A monoclonal antibody, an anti-zearalenone monoclonal antibody and an anti-sterigmatocystin monoclonal antibody which are coupled to the solid-phase support, wherein the anti-fumonisin Bmonoclonal antibody is secreted by a hybridoma cell strain Fm7A11, and the hybridoma cell strain Fm7A11 has been preserved at China Center for Type Culture Collection, Wuhan University, Wuhan, China on Mar. 29, 2016 with the preservation number of CCTCC No. C201636. The complex affinity column can be used for purification and detection of a fumonisin Bsample, an aflatoxin Bsample, an ochratoxin A sample, a zearalenone sample and a sterigmatocystin sample at the same time. 1. An immunoadsorbent for purifying fumonisin B , aflatoxin B , ochratoxin A , zearalenone and sterigmatocystin , comprisinga solid-phase support, and{'sub': 1', '1, 'an anti-fumonisin Bmonoclonal antibody, an anti-aflatoxin Bmonoclonal antibody, an anti-ochratoxin A monoclonal antibody, an anti-zearalenone monoclonal antibody and an anti-sterigmatocystin monoclonal antibody which are coupled to the solid-phase support,'}{'sub': '1', 'wherein the anti-fumonisin Bmonoclonal antibody is secreted by a hybridoma cell strain Fm7A11, and the hybridoma cell strain Fm7A11 has been preserved at China Center for Type Culture Collection, Wuhan University, Wuhan, China on Mar. 29, 2016 with the preservation number of CCTCC No. C201636.'}2. The immunoadsorbent according to claim 1 , wherein the solid-phase support is a sepharose.3. A complex affinity column loaded with the immunoadsorbent according to claim for purifying fumonisin B claim 1 , aflatoxin B claim 1 , ochratoxin A claim 1 , zearalenone and sterigmatocystin.4. A ...

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21-10-2021 дата публикации

Superabsorbent Polymer Composition And Method For Preparing The Same

Номер: US20210322953A1
Принадлежит: LG CHEM, LTD.

The invention relates to superabsorbent polymer that not only has excellent basic absorption performance, but also exhibits more improved permeability under pressure, and thus, can improve rewet property and leak inhibition property of hygienic products such as a diaper, and the like, and a method for preparing the same. The superabsorbent polymer comprises base resin powder comprising first crosslinked polymer of water soluble ethylenically unsaturated monomers having acid groups of which at least a part are neutralized; and a surface crosslink layer on the base resin powder, comprising second crosslinked polymer formed by additional crosslinking of the first crosslinked polymer by a surface crosslinking agent, wherein the surface crosslinking agent comprises a polymer type first surface crosslinking agent having number average molecular weight of 300 or more, and having plural hydroxy groups or epoxy groups. 1. A superabsorbent polymer comprising:a base resin powder comprising a first crosslinked polymer of water soluble ethylenically unsaturated monomers having acid groups of which at least a part are neutralized; anda surface crosslink layer on the base resin powder, comprising a second crosslinked polymer formed by additional crosslinking of the first crosslinked polymer by a surface crosslinking agent,wherein the surface crosslinking agent comprises a polymer first surface crosslinking agent having a number average molecular weight of 300 or more, and having plural hydroxy groups or epoxy groups.2. The superabsorbent polymer according to claim 1 , wherein the surface crosslinking agent further comprises a second surface crosslinking agent having a molecular weight less than 300 claim 1 , comprising:one or more polyols selected from the group consisting of ethylene glycol, propylene glycol, 1,3-propanediol, 1,4-butanediol, 1,6-hexanediol, 1,2-hexanediol, 1,3-hexanediol, 2-methyl-1,3-propanediol, 2,5-hexanediol, 2-methyl-1,3-pentanediol, 2-methyl-2,4-pentanediol ...

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22-09-2016 дата публикации

Protein Separations Using An Acrylamide Containing Filter

Номер: US20160272676A1
Принадлежит:

Novel compositions for re-moving impurities such as, protein aggregates, from a sample containing a protein of interest, e.g., an antibody. Such compositions can be used prior to the virus filtration step during protein purification, to remove aggregates and protect the virus filter from fouling, therefore improving virus filter capacity. A porous solid support including a co-polymer having at least two monomers, wherein at least one of the monomers comprises acrylamide and at least a second monomer comprises a hydrophobic binding group, where the solid support selectively binds protein aggregates, thereby to separate the monomeric protein of interest from the protein aggregates. The method can be performed under neutral to high pH and high conductivity conditions. 2. A method of separating a monomeric protein of interest from protein aggregates in a sample , the method comprising contacting the sample with a porous solid support comprising a co-polymer of benzyl acrylamide and acrylamide , wherein the solid support selectively binds protein aggregates , thereby separating the monomeric protein of interest from the protein aggregates.3. The method of wherein the method is performed at neutral to higher pH of 6 or greater.4. The method of wherein the method is performed in a solution of moderate to high conductivity of 5 mS/cm or greater.5. The method of claim 2 , wherein the solid support is selected from the group consisting of chromatographic resin claim 2 , a membrane claim 2 , a porous bead claim 2 , a porous monolith claim 2 , a winged fiber claim 2 , a woven fabric and a non-woven fabric.6. The method of claim 2 , wherein the protein aggregates are lower order protein aggregates.7. The method of claim 6 , wherein the lower order protein aggregates are selected from the group consisting of dimers claim 6 , trimers claim 6 , and tetramers.8. The method of claim 2 , wherein the protein aggregates are high molecular weight protein aggregates.9. The method of claim ...

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22-08-2019 дата публикации

Carrier for ligand immobilization

Номер: US20190256555A1
Принадлежит: Kaneka Corp

A carrier for ligand immobilization obtained by shrinking polysaccharide porous beads not less than 10% by a shrinkage rate defined by the following formula, and crosslinking the polysaccharide porous beads: Shrinkage rate (%)=(1−V 2 /V 1 )×100 (wherein, V 1 indicates the gel volume of polysaccharide porous beads before shrinkage, and V 2 indicates the gel volume of polysaccharide porous beads after shrinkage).

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08-10-2015 дата публикации

IMMOBILISATION OF CHELATING GROUPS FOR IMMOBILISED METAL ION CHROMATOGRAPHY (IMAC)

Номер: US20150283536A1

The present invention refers to a method for binding a polycarboxylic acid to a solid phase. Further, the invention refers to a solid phase having a polycarboxylic acid immobilized thereto and methods of using the solid phase, e.g. for purifying His-tagged recombinant polypeptides. 121-. (canceled)22. A method for immobilized metal ion chromatography (IMAC) , comprising contacting a sample with an immobilized chelator having 6 or more coordination groups.23. The method of claim 22 , wherein the immobilized chelator is a polycarboxylic acid amide or ester having 6 or more coordination groups.24. The method according to claim 23 , wherein said coordination groups are selected from the group consisting of amino claim 23 , carboxyl claim 23 , carboxamide and hydroxamate groups.26. The method of claim 25 , wherein said PCA is the residue of an amino polycarboxylic acid or a salt thereof.27. The method of claim 25 , wherein the polycarboxylic acid is selected from the group consisting of ethylene diamino tetraacetic acid (EDTA) claim 25 , ethylene glycol-bis(2-aminoethylether)-N claim 25 ,N claim 25 ,N′ claim 25 ,N′-tetraacetic acid (EGTA) claim 25 , diethylene triamino pentaacetic acid (DPTA) claim 25 , and triethylene tetramine-N claim 25 ,N claim 25 ,N′ claim 25 ,N′ claim 25 , N″ claim 25 ,N″-hexa-acetic acid (TTHA) claim 25 , salts thereof.28. The method according to claim 27 , wherein said polycarboxylic acid is ethylene diamino tetraacetic acid (EDTA).30. The method of claim 22 , wherein the chelator is complexed with a metal ion.31. The method according to claim 30 , wherein said metal ion is a transition metal ion.32. The method according to claim 31 , wherein said transition metal a Ni ion.33. A method for binding a polycarboxylic acid having 6 or more coordination groups to a solid phase claim 31 , comprising the steps:(a) providing a polycarboxylic acid and a solid phase comprising amino groups,(b) reacting the amino groups with the polycarboxylic acid in the ...

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12-09-2019 дата публикации

FC-RECEPTOR BASED AFFINITY CHROMATOGRAPHY

Номер: US20190276492A1
Принадлежит:

Herein is reported the use of an immobilized non-covalent complex of a neonatal Fc receptor (FcRn) and beta-2-microglobulin (b2m) as affinity chromatography ligand in general and, for example, for the determination of the in vivo half-live of an antibody by determining the ratio of the retention times of the antibody and a reference antibody. 137.-. (canceled)38. A method for determining the in vivo half-live of an antibody in relation to a full length human IgG1 antibody by determining the ratio of the retention times determined on an FcRn affinity column comprising a non-covalent complex of neonatal Fc receptor (FcRn) and beta-2-microglobulin as ligand of said antibody and said full length human IgG1 antibody with a positive linear pH gradient.39. The method according to claim 38 , wherein the neonatal Fc receptor and the beta-2-microglobulin are independently of each other of human origin claim 38 , or of mouse origin claim 38 , or of cynomolgus origin claim 38 , or of rat origin claim 38 , or of rabbit origin40. The method according to claim 38 , wherein the beta-2-microglobulin is from the same species as the neonatal Fc receptor.41. The method according to claim 38 , wherein the neonatal Fc receptor and the beta-2-microglobulin are the human wild-type neonatal Fc receptor and the human wild-type beta-2-microglobulin each independently of each other with 0 to 10 amino acid residue modifications.42. The method according to claim 38 , wherein the non-covalent complex of a neonatal Fc receptor (FcRn) and beta-2-microglobulin (b2m) is bound to a solid phase.43. The method according to claim 38 , wherein the positive linear pH gradient is from a first pH value to a second pH value whereby the first pH value is from about pH 3.5 to about pH 7.5 and the second pH value is from about pH 6.0 to about pH 9.5.44. The method according to claim 38 , wherein the positive linear pH gradient is from about pH 5.5 to about pH 8.8.45. The method according to claim 38 , wherein ...

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22-10-2015 дата публикации

Multimodal Anion Exchange Matrices

Номер: US20150299248A1
Принадлежит: GE Healtchare Bio-Sciences AB

The invention discloses a separation matrix which comprises a plurality of separation ligands, defined by the formula R-L-N(R)-L-R, immobilized on a support, wherein Ris a five- or six-membered, substituted or non-substituted ring structure or a hydroxyethyl or hydroxypropyl group; Lis either a methylene group or a covalent bond; Ris a five- or six-membered, substituted or non-substituted ring structure; Lis either a methylene group or a covalent bond; Ris a methyl group; and wherein if Ris a hydroxyethyl group and Lis a covalent bond, Ris a substituted aromatic ring structure or a substituted or non-substituted aliphatic ring structure. 1. A separation matrix comprising a plurality of separation ligands defined by formula (I){'br': None, 'sub': 1', '1', '3', '2', '2, 'R-L-N(R)-L-R\u2003\u2003(I)'}immobilized on a support,wherein{'sub': '1', 'Ris a five- or six-membered, substituted or non-substituted ring structure or a hydroxyethyl or hydroxypropyl group;'}{'sub': '1', 'Lis either a methylene group or a covalent bond;'}{'sub': '2', 'Ris a five- or six-membered, substituted or non-substituted ring structure;'}{'sub': '2', 'Lis either a methylene group or a covalent bond;'}{'sub': '3', 'Ris a methyl group;'}{'sub': 1', '1', '2, 'and wherein if Ris a hydroxyethyl group and Lis a covalent bond, Ris a substituted aromatic ring structure or a substituted or non-substituted aliphatic ring structure.'}2. The separation matrix according to claim 1 , wherein the ligands are immobilized via the amine group.3. The separation matrix according to claim 1 , wherein said ligands in free form have an octanol-water distribution coefficient (lg P) of 1.8 or higher claim 1 , such as 1.8-5 claim 1 , 1.8-4 claim 1 , 2-4 claim 1 , 1.8-3 or 2-3.4. The separation matrix according to claim 1 , wherein Ris a substituted or non-substituted phenyl or cyclohexyl ring structure.5. The separation matrix according to claim 1 , wherein Rcomprises one or more methyl claim 1 , methoxy claim 1 , or ...

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