EP1761592A1 - Verfahren zur herstellung von polymeren trägermaterialien auf basis von kohlenhydrat-bis- (meth)acrylamiden - Google Patents
Verfahren zur herstellung von polymeren trägermaterialien auf basis von kohlenhydrat-bis- (meth)acrylamidenInfo
- Publication number
- EP1761592A1 EP1761592A1 EP05752320A EP05752320A EP1761592A1 EP 1761592 A1 EP1761592 A1 EP 1761592A1 EP 05752320 A EP05752320 A EP 05752320A EP 05752320 A EP05752320 A EP 05752320A EP 1761592 A1 EP1761592 A1 EP 1761592A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- radical
- methyl
- bis
- groups
- meth
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F222/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a carboxyl radical and containing at least one other carboxyl radical in the molecule; Salts, anhydrides, esters, amides, imides, or nitriles thereof
- C08F222/36—Amides or imides
- C08F222/38—Amides
- C08F222/385—Monomers containing two or more (meth)acrylamide groups, e.g. N,N'-methylenebisacrylamide
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
- B01J20/22—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising organic material
- B01J20/26—Synthetic macromolecular compounds
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
- B01J20/22—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising organic material
- B01J20/26—Synthetic macromolecular compounds
- B01J20/261—Synthetic macromolecular compounds obtained by reactions only involving carbon to carbon unsaturated bonds
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
- B01J20/281—Sorbents specially adapted for preparative, analytical or investigative chromatography
- B01J20/282—Porous sorbents
- B01J20/285—Porous sorbents based on polymers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
- B01J20/30—Processes for preparing, regenerating, or reactivating
- B01J20/32—Impregnating or coating ; Solid sorbent compositions obtained from processes involving impregnating or coating
- B01J20/3202—Impregnating or coating ; Solid sorbent compositions obtained from processes involving impregnating or coating characterised by the carrier, support or substrate used for impregnation or coating
- B01J20/3206—Organic carriers, supports or substrates
- B01J20/3208—Polymeric carriers, supports or substrates
- B01J20/321—Polymeric carriers, supports or substrates consisting of a polymer obtained by reactions involving only carbon to carbon unsaturated bonds
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D15/00—Separating processes involving the treatment of liquids with solid sorbents; Apparatus therefor
- B01D15/08—Selective adsorption, e.g. chromatography
- B01D15/26—Selective adsorption, e.g. chromatography characterised by the separation mechanism
- B01D15/38—Selective adsorption, e.g. chromatography characterised by the separation mechanism involving specific interaction not covered by one or more of groups B01D15/265 - B01D15/36
- B01D15/3804—Affinity chromatography
Definitions
- the invention relates to a process for the preparation of novel polymeric support materials based on (meth) acrylamide-substituted carbohydrates and their use for affinity chromatography or solid-phase syntheses.
- the morphology (pore diameter, internal surface area, particle size) is predetermined and can only be controlled to a very limited extent; moreover, their mechanical stability is usually insufficient for continuous column operation.
- Sucrose methacrylate supports are obtained by precipitation polymerization and are only weakly cross-linked, resulting exclusively in gel types. Although is here because of the water solubility of the low-substituted monomer mixtures also given the possibility of inverse suspension polymerization, but the possibilities of reaction control are very limited with this method, since most water-compatible pore former for controlling the morphology strongly affect the solubility of the monomer mixtures and thus the degree of crosslinking not can be adjusted more. Even with glucose monomethacrylate supports, the hydrophilicity can only be varied within relatively narrow limits because of the small number of hydroxyl groups.
- the object of the present invention is the provision of polymeric supports in the preparation of which morphology (particle size, porosity), degree of crosslinking, and swellability in aqueous and organic media can be tailored, whose reactive groups offer versatile possibilities for the immobilization of anchor and protective groups, and which are thermally and hydrolytically stable.
- the invention relates to a process for the preparation of polymeric carriers based on polyacrylic or Polymethacrylklareamiden of monosaccharides, characterized in that acrylic or methacrylamide derivatives of carbohydrates with protected HO groups of the general formula I.
- R is hydrogen or a CH 3 group, and at least one X is the group -CO-CH 3 , -CH 2 -C 6 H 5 , -Si (CH 3 ) 3 , or at least two groups X together for the rest
- R 1 and R 2 independently of one another are hydrogen, an alkyl radical having 1 to 10 C atoms or an aromatic radical
- R 3 is a cycloalkyl radical having 4 to 10 C atoms or a phenyl radical
- the remaining X is hydrogen
- Y is the radical -NH-, -CH 2 -NH-, or -CO-NR 4 -Z-NR 5 -
- R 4 and R 5 are independently hydrogen, an alkyl radical having 1 to 10 carbon atoms or an aromatic radical polymerized - optionally in the presence of pore-forming additives - and then from the resulting crosslinked
- Protected carbohydrate diamines whose protective groups can be split off under mild conditions, such as. eg 1, 6-diamino-1,6-dideoxy-2,3: 4,5-di-O-isopropylidene-galactitol, or 1,6-diamino-1,6-dideoxy- 2,3: 4,5-di-O-benzylidene-galactitol.
- These diamines can be prepared according to US Pat. 3 463 790 (1969) are prepared from the corresponding 1,6-dichloro derivatives, although relatively low overall yields are achieved. According to a hitherto unknown synthetic route, these diamines are also prepared from the - also not yet described - dimethyl galactarate in 64% Total yield obtained.
- new carbohydrate diamines which are prepared by reacting aldaric acid dialkyl esters with excess diamines.
- galactaric acid dimethyl ester is first protected with 2,2-dimethoxypropane and the resulting 2,3: 4,5-di-O-isopropylidene-galactaric acid dimethyl ester with excess ethylenediamine to 2,3: 4,5-di-O-isopropylidene-galactaric acid reacted bis (2-aminoethyl) amide.
- diamines used in this synthesis a large number of new carbohydrate diamines can be obtained easily and in high yields.
- aliphatic diamines having 2 to 20 C atoms such as. B ethylenediamine, hexamethylenediamine, 1,12-diaminododecane, 1,2-bis (aminoethoxy) ethane or piperazine.
- the properties of the resulting carbohydrate-diamine and thus of the polymer carrier can also be influenced. If, for example, in the synthesis of the carbohydrate diamine 1, 12-dodecanediamine, results after methacryloylation and polymerization, a carrier whose HO groups are more accessible due to low steric hindrance for further reactions. On the other hand, aromatic radicals increase the thermal stability of the polymeric carrier.
- the aldaric acid alkyl ester may also be provided with other protecting groups known from the chemistry of carbohydrates, e.g. Acetate, trimethylsilyl, benzylidene or cyclohexylidene groups.
- the reaction with diamines can also be carried out with unprotected aldaric acid alkyl esters.
- the protected carbohydrate diamines are then reacted with (meth) acrylic acid derivatives to methacrylamides.
- (meth) acrylic acid, its esters, (meth) acryloyl chloride or methacrylic anhydride can be used.
- the carbohydrate diamine is used with the (meth) acrylic acid derivative at least in a molar ratio of 1: 2, lower molar ratios lead to mixtures of mono- and bis (meth) acrylamides, which however can also be used according to the invention for the polymerization.
- the crosslinked polymeric support can be prepared from these monomers or monomer mixtures, for example, by suspension polymerization in aqueous media. Furthermore, the morphology can be controlled in a targeted manner by adding suitable pore formers (porogens). By varying the degree of crosslinking and / or the pore-forming agent, gel types, microporous or even macroporous carriers can be produced in this way.
- suitable pore formers porogens
- the monomer mixture is dissolved in a water-immiscible solvent, optionally a pore-forming agent, such as toluene or n-octanol added (the pore former may also act as a solvent for the monomer), and after addition of a radical initiator and a suspension stabilizer with stirring in aqueous suspension polyrnerinstrument.
- the polymerization temperature is determined by the half-life of the initiator used.
- the resulting polymer particles, whose size can be controlled by the stirring speed, are filtered off, washed several times with suitable solvents and dried.
- the resulting polymers are hydrophobic because of the protective groups still contained and non-swellable in water.
- the polymer particles are treated with suitable reagents, for example in the case of isopropylidene-protected monomers with trifluoroacetic acid or acetic acid, in the case of the acetylated monomers by mild alkaline treatment for selective cleavage of the acetyl groups (eg. With 0.02 N sodium Solution in methanol).
- suitable reagents for example in the case of isopropylidene-protected monomers with trifluoroacetic acid or acetic acid, in the case of the acetylated monomers by mild alkaline treatment for selective cleavage of the acetyl groups (eg. With 0.02 N sodium Solution in methanol).
- the polymerization of the monomers according to the invention can also be carried out in the presence of other monomers, such as.
- (meth) acrylic acid For example, (meth) acrylic acid, (meth) acrylic acid esters, styrene, vinyl acetate, N-vinylpyrrolidone and other known monomers.
- the invention thus also relates to polymeric carriers which, in addition to other monomer units, have structural elements of the formula II
- the carriers of the invention can be activated via the HO groups by known methods. For example, high loading can be achieved for the solid phase synthesis of peptides by direct condensation of amino acids on the HO groups of the carriers. If in solid phase synthesis strong acids, e.g. Trifluoroacetic acid used, it may possibly lead to unwanted separation of the peptides from the polymer carrier. In this case, it is expedient to introduce amino groups into the carrier and to protect the remaining HO groups before coupling the first amino acid.
- strong acids e.g. Trifluoroacetic acid used
- peptide syntheses can also be carried out, for example, by the Fmoc "double-coupling" routine in dimethylformamide using Na-Fmoc-protected amino acids, benzotriazol-1-yl-oxytris (dimethylamino) phosphonium hexafluorophosphate (BOP ) and N-hydroxybenzotriazole (HOBt) can be used as condensation reagents and diisopropylethylamine (DIPEA) as the base Examples
- aqueous phase 144 g of water 14.4 g of sodium chloride 0.23 g of hydroxyethylcellulose (Tylose) organic phase: 9.00 g of monomer (see 1d) porogen (type and amount, see Table 1) 0.1 g of azodiisobutyronitrile (AIBN)
- Example 1e The procedure of Example 1e) is repeated, with the difference that the monomer 2b) is used. Depending on the porogen used, yields of 60 to 85% polymer are obtained, with BET surface areas of 0.5 to 70.6 m 2 / g.
Landscapes
- Chemical & Material Sciences (AREA)
- Analytical Chemistry (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Peptides Or Proteins (AREA)
Abstract
Description
Claims
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AT0110004A AT413102B (de) | 2004-06-29 | 2004-06-29 | Verfahren zur herstellung von polymeren trägermaterialien auf basis von kohlenhydrat-bis-(meth)acrylamiden |
PCT/AT2005/000230 WO2006000008A1 (de) | 2004-06-29 | 2005-06-24 | Verfahren zur herstellung von polymeren trägermaterialien auf basis von kohlenhydrat-bis- (meth)acrylamiden |
Publications (1)
Publication Number | Publication Date |
---|---|
EP1761592A1 true EP1761592A1 (de) | 2007-03-14 |
Family
ID=34427291
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP05752320A Withdrawn EP1761592A1 (de) | 2004-06-29 | 2005-06-24 | Verfahren zur herstellung von polymeren trägermaterialien auf basis von kohlenhydrat-bis- (meth)acrylamiden |
Country Status (7)
Country | Link |
---|---|
US (1) | US7674839B2 (de) |
EP (1) | EP1761592A1 (de) |
JP (1) | JP2008504410A (de) |
CN (1) | CN1997694B (de) |
AT (1) | AT413102B (de) |
CA (1) | CA2572142A1 (de) |
WO (1) | WO2006000008A1 (de) |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN106883334B (zh) | 2012-02-09 | 2019-06-18 | 生命技术公司 | 亲水性聚合物颗粒及其制备方法 |
EP3640254A1 (de) * | 2012-02-09 | 2020-04-22 | Life Technologies Corporation | Hydrophobe diacrylamidverbindung |
CN103908935B (zh) * | 2014-03-21 | 2016-02-10 | 中国科学院长春应用化学研究所 | 一种玻璃毛细管微流装置及使用该装置制备具有多级孔道结构的聚合物微球的方法 |
JP2017536224A (ja) * | 2014-09-29 | 2017-12-07 | レノビア インコーポレイテッド | ジカルボン酸塩型の陰イオン交換クロマトグラフィー樹脂を用いるジカルボン酸含有混合物の調製および分離 |
TW201632993A (zh) * | 2015-01-05 | 2016-09-16 | 巴地斯顏料化工廠 | Led可固化之低遷移光起始劑 |
EP3317314B1 (de) | 2015-07-02 | 2020-01-08 | Life Technologies Corporation | Polymersubstrate aus carboxyfunktionellem acrylamid |
CN108884224B (zh) * | 2016-03-30 | 2021-09-10 | 国立大学法人东京大学 | 以醛糖二酸为结构单元的新型聚合物和制造方法 |
EP3312168A1 (de) * | 2016-10-19 | 2018-04-25 | Koninklijke Coöperatie Cosun U.A. | Bis-diox(ol)an-verbindungen |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3463790A (en) | 1962-09-20 | 1969-08-26 | Us Agriculture | 1,6-diamino-2,3:4,5-di-o-benzylidine-1,6-dideoxygalactitol |
US3420852A (en) | 1962-09-20 | 1969-01-07 | Us Agriculture | Dichloride salts of o-methylenated sugar acids |
US4060506A (en) * | 1976-04-27 | 1977-11-29 | A. E. Staley Manufacturing Company | Starch acrylamides and the method for preparing the same |
JPS57202309A (en) * | 1981-06-05 | 1982-12-11 | Agency Of Ind Science & Technol | Polyacrylamide derivative having monosaccharide residue |
JPS62116617A (ja) * | 1985-11-18 | 1987-05-28 | Dainippon Ink & Chem Inc | 共重合体エマルジヨン |
ES2073412T3 (es) | 1988-10-19 | 1995-08-16 | Guest Elchrom Scient Ag | Monomeros hidrofilos, sus polimeros y sus utilizaciones. |
US5278270A (en) * | 1990-04-20 | 1994-01-11 | Branko Kozulic | Hydrophilic and amphiphatic monomers, their polymers and gels and hydrophobic electrophoresis |
DE4005868A1 (de) * | 1990-02-24 | 1991-08-29 | Merck Patent Gmbh | Trennmaterialien |
TW291481B (en) * | 1994-10-27 | 1996-11-21 | Novartis Erfind Verwalt Gmbh | Poly-unsaturated carbohydrate derivatives, polymers thereof and their use |
US6018033A (en) * | 1997-05-13 | 2000-01-25 | Purdue Research Foundation | Hydrophilic, hydrophobic, and thermoreversible saccharide gels and forms, and methods for producing same |
US6107365A (en) * | 1997-09-03 | 2000-08-22 | The Regents Of The University Of California | Biomimetic hydrogel materials |
-
2004
- 2004-06-29 AT AT0110004A patent/AT413102B/de not_active IP Right Cessation
-
2005
- 2005-06-24 CA CA002572142A patent/CA2572142A1/en not_active Abandoned
- 2005-06-24 WO PCT/AT2005/000230 patent/WO2006000008A1/de not_active Application Discontinuation
- 2005-06-24 US US11/631,236 patent/US7674839B2/en not_active Expired - Fee Related
- 2005-06-24 EP EP05752320A patent/EP1761592A1/de not_active Withdrawn
- 2005-06-24 CN CN200580021898XA patent/CN1997694B/zh not_active Expired - Fee Related
- 2005-06-24 JP JP2007518406A patent/JP2008504410A/ja active Pending
Non-Patent Citations (1)
Title |
---|
See references of WO2006000008A1 * |
Also Published As
Publication number | Publication date |
---|---|
US7674839B2 (en) | 2010-03-09 |
WO2006000008A1 (de) | 2006-01-05 |
JP2008504410A (ja) | 2008-02-14 |
CN1997694A (zh) | 2007-07-11 |
US20080300383A1 (en) | 2008-12-04 |
CA2572142A1 (en) | 2006-01-05 |
AT413102B (de) | 2005-11-15 |
CN1997694B (zh) | 2011-06-15 |
ATA11002004A (de) | 2005-04-15 |
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