Process for synthesis of bead-shaped cross-linked hydrophilic support polymer
원문보기
IPC분류정보
국가/구분
United States(US) Patent
등록
국제특허분류(IPC7판)
C12N-011/08
C12N-011/00
C12P-001/00
G01N-033/545
G01N-033/544
C07K-017/08
C07K-017/00
A61K-009/14
출원번호
US-0600180
(1999-02-01)
우선권정보
DE-198 04 518(1998-02-05)
국제출원번호
PCT/EP99/000635
(1999-02-01)
§371/§102 date
20011221
(20011221)
국제공개번호
WO99/040122
(1999-08-12)
발명자
/ 주소
Meier,Christian
Suefke,Thomas
Petereit,Hans Ulrich
Recktenwald,Roger
Boller,Thomas
출원인 / 주소
Roehm GmbH &
Co KG
대리인 / 주소
Oblon, Spivak, McClelland, Maier &
인용정보
피인용 횟수 :
3인용 특허 :
6
초록▼
The invention relates to a process for synthesis, by inverse bead polymerization of a monomer phase, of a bead-like, cross-linked, hydrophilic copolymer which has binding activity toward ligands containing nucleophilic groups. The invention relates to support polymer materials with high binding capa
The invention relates to a process for synthesis, by inverse bead polymerization of a monomer phase, of a bead-like, cross-linked, hydrophilic copolymer which has binding activity toward ligands containing nucleophilic groups. The invention relates to support polymer materials with high binding capacity for penicillin acylase and low swelling factor, as well as to use of the same.
대표청구항▼
What is claimed is: 1. A process for the synthesis of a bead-shaped, cross-linked, hydrophilic copolymer, comprising: radically polymerizing a monomer phase, in a bead polymerization process, in the presence of a polymerization initiator and a protective colloid, the monomer phase comprising: mono
What is claimed is: 1. A process for the synthesis of a bead-shaped, cross-linked, hydrophilic copolymer, comprising: radically polymerizing a monomer phase, in a bead polymerization process, in the presence of a polymerization initiator and a protective colloid, the monomer phase comprising: monomers, and a diluent, the monomer phase being present during the polymerization in dispersed form as droplets in a dispersion medium comprising an organic solvent selected from the group consisting of aliphatic hydrocarbons with 5 to 7 carbon atoms; to thereby obtain said bead-shaped, cross-linked, hydrophilic copolymer, the copolymer having a binding activity toward ligands containing nucleophilic groups, wherein said monomer phase comprises as monomers a) 5 to 40 wt % of hydrophilic monomers which contain a vinyl group, said hydrophilic monomers being capable of radical polymerization, and being capable of forming at least 10% aqueous solutions at room temperature, b) 30 to 50 wt % of monomers which contain a vinyl group and an additional functional group, said monomers being capable of radical polymerization and being capable of forming at least one covalent bond in a reaction with at least one nucleophilic group of a ligand, and c) 20 to 60 wt % of cross-linking monomers which contain two or more ethylenically unsaturated polymerizable groups, said cross-linking monomers being capable of radical polymerization, wherein a), b) and c) add up to 100 wt %, wherein said monomer phase comprises as diluent a mixture of methanol and water in the ratio of 1:1.0 to 1:4.0, wherein a ratio of monomer phase to dispersion medium ranges from 1:2.0 to 1:4.0, and wherein a ratio of monomers to diluent ranges from 1:1.7 to 1:2.4. 2. The process according to claim 1, wherein said monomers are a) acrylamide, methacrylamide or mixtures thereof, b) glycidyl methacrylate, allyl glycidyl ether or mixtures thereof, c) methylenebisacrylamide or methylenebismethacrylamide. 3. The process according to claim 1, wherein said organic solvent is cyclohexane. 4. The process according to claim 1, wherein said monomer a) is a methacrylamide. 5. The process according to claim 1, wherein said functional group of monomer b) is an oxirane group. 6. The process according to claim 1, wherein said ligand of said nucleophilic group is an oxirane group. 7. The process according to claim 1, wherein said monomer c) is N, N'-methylenebismethacrylamide. 8. The process according to claim 1, wherein said ratio of monomers to diluent is from 1:1.9 to 1:2.1. 9. The process according to claim 1, wherein said ratio of monomer phase to dispersion medium is from 1:2.8 to 1:3.3. 10. The process according to claim 1, wherein said protective colloid is a copolymer comprising 95 parts of n-butyl methacrylate and 5 parts of 2-trimethylammoniumethyl methacrylate chloride having a weight average molecular weight of from 30,000 to 80,000. 11. The process according to claim 1, wherein said copolymer has a size of from 50 to 500 μm. 12. A support polymer material obtained by the process according to claim 1, said support polymer having a binding capacity for penicillin amidase from E. coli of at least 220 U/g moist, based on a reaction of 1530 units of penicillin amidase with 1 g of said support polymer material, and said support polymer having a swelling factor of at most 1.5. 13. A method of binding proteins, comprising: contacting the support polymer material according to claim 12, with at least one protein. 14. A method of binding enzymes, comprising: contacting the support polymer material according to claim 12 with at least one enzyme. 15. A method of binding antibodies, comprising: contacting the support polymer material according to claim 12 with at least one antibody. 16. A method of chromatography, comprising: contacting the support polymer material according to claim 12 with at least one compound. 17. A method for synthesis of pharmaceuticals, comprising: synthezising a pharmaceutical in the presence of the support polymer material according to claim 12. 18. A method for stereospecific synthesis of chiral substances, comprising: synthezising a chiral substance in the presence of the support polymer material according to claim 12. 19. A method of covalently binding of a ligand, comprising: contacting the support polymer material according to claim 12 with a ligand to covalently bind the ligand to the support polymer material; wherein said support polymer material has an oxirane group. 20. A support polymer material loaded with a ligand and obtained by the method according to claim 19.
Kleese Wolfgang (Mainz DEX) Kraemer Dieter (Mainz DEX) Petereit Hans-Ulrich (Darmstadt DEX) Lehmann Klaus (Rossdorf DEX) Siol Werner (Darmstadt-Eberstadt DEX), Method for making carrier systems for biologically active materials.
Menzler,Stefan; Petereit,Hans Ulrich; Meier,Christian; Boller,Thomas; Suefke,Thomas; Schultes,Klaus; Recktenwald,Roger, Macroporous material in the form of plastic pearls.
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