IPC분류정보
| 국가/구분 |
United States(US) Patent
등록
|
| 국제특허분류(IPC7판) |
|
| 출원번호 |
US-0399847
(2009-03-06)
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| 등록번호 |
US-8378022
(2013-02-19)
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|
발명자
/ 주소 |
- Bucevschi, Mircea Dan
- Colt, Monica
- Axlerad, Mendy
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| 출원인 / 주소 |
- Exotech Bio Solutions Ltd.
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| 인용정보 |
피인용 횟수 :
0 인용 특허 :
43 |
초록
▼
A biocompatible, biodegradable, macromolecular water-absorbent hybrid material (WAHM), having a three-dimensional configuration with intermolecular covalent bonds and containing free functional groups, said polymer being formed by polymer-polymer intercoupling reaction between a natural water-solubl
A biocompatible, biodegradable, macromolecular water-absorbent hybrid material (WAHM), having a three-dimensional configuration with intermolecular covalent bonds and containing free functional groups, said polymer being formed by polymer-polymer intercoupling reaction between a natural water-soluble polymer A or its derivatives having a molecular weight between 20,000 and 300,000 Da, and a synthetic polymer B in an adequate ratio wherein the natural polymer A is selected from amphoteric reactants, partially denatured or chemically modified natural polymer, that dissociates in water to form both anions and cations, and which can undergo polymer-polymer intercoupling reactions, and wherein synthetic polymer B s a linear or branched reactive synthetic copolymer having a molecular weight of 50,000-500,000 Da derived from a vinyl monomer and an ethylenically unsaturated monomer, having a backbone with polymeric subunits covalently bonded to the polymer backbone, the subunits comprising ones with non-reactive and others with reactive chemical functional groups.
대표청구항
▼
1. A process for preparing a biocompatible, biodegradable, macromolecular water-absorbent hybrid material, having a three-dimensional configuration with intermolecular covalent bonds and containing free functional groups selected from OH, SH, NH2 and COOH, said polymer being formed by polymer-polyme
1. A process for preparing a biocompatible, biodegradable, macromolecular water-absorbent hybrid material, having a three-dimensional configuration with intermolecular covalent bonds and containing free functional groups selected from OH, SH, NH2 and COOH, said polymer being formed by polymer-polymer intercoupling reaction between a natural water-soluble polymer A or a derivative thereof having a molecular weight between 20,000 and 300,000Da, and a synthetic polymer B in a ratio of A to B between 1 and 50% of the dry mixture (A+B), wherein the natural polymer A is selected from: amphoteric reactants, partially denatured or chemically modified natural polymers, that dissociate in water to form both anions and cations, and which can undergo polymer-polymer intercoupling reactions, and wherein: synthetic polymer B is a linear or branched reactive synthetic copolymer having a molecular weight of 50,000-500,000Da derived from a vinyl monomer and an ethylenically unsaturated monomer, said copolymer having a backbone with polymeric subunits Rn and Rr , wherein R represents a subunit covalently bonded to the polymer backbone, n represents nonreactive chemical functional groups and r represents reactive chemical functional groups said method comprising reacting a solution of the natural polymer A in water with a suspension of the synthetic polymer B in water in the absence of a cross linking or coupling agent, thereby forming the biocompatible, biodegradable, macromolecular water-absorbent hybrid material. 2. A method for preparing a biocompatible, biodegradable, macromolecular water absorbent hybrid material having a three-dimensional configuration with intermolecular covalent bonds and containing free functional groups selected from the group consisting of —OH, —SH, —NH2 and —COOH, comprising reacting an aqueous solution of a natural water-soluble polymer A with an aqueous suspension of a synthetic polymer B to form a water-absorbent hybrid material by a polymer-polymer intercoupling reaction. 3. Method according to claim 2, wherein said polymer-polymer intercoupling reaction is conducted at a temperature in the range of 35-55 degrees Celsius. 4. The method of claim 2, further comprising washing said synthetic polymer B with water prior to reacting said synthetic polymer B with said natural water-soluble polymer A. 5. The method of claim 2 wherein the natural polymer is collagen, a collagenic biopolymer, gelatin, gelatin modified by reaction with an anhydride or acid chloride, alfa-keratose, gamma-keratose, keratin hydrolysate, elastin, fibrin, casein, or soybean protein. 6. The method of claim 5, wherein the natural polymer is gelatin. 7. The method of claim 6, wherein the synthetic polymer is poly(styrene-co-maleic anhydride). 8. Method according to claim 2, wherein said natural water-soluble polymer A is a protein modified by reaction with an anhydride or acid chloride. 9. The method of claim 2, wherein the synthetic polymer B is poly (ethylene-alt-maleic anhydride), poly (ethylene-graft-maleic anhydride), poly (isobutylene-co-maleic anhydride), poly(isoprenegraft-maleic anhydride), poly (maleic anhydride-co-1-octadecene), polypropylene-graft-maleic anhydride), or poly (styrene-co-maleic anhydride). 10. The method of claim 2, wherein the natural polymer has at least 1×10−3 moles —COOH/g and at least 0.5×10−3 moles —NH2/g, and said natural polymer has an isoelectric point of not less than 2.5 and not more than 10.5. 11. The method of claim 2, wherein the ionic reactive chemical functionality of polymer B is not less than 5×10−3 moles “r”/g and not more than 1×10−2 moles “r”/g. 12. The method of claim 2, wherein said polymer-polymer intercoupling reaction is conducted in the presence of a base. 13. The method of claim 12, wherein said base is NaOH, NH3, or LiOH. 14. The process of claim 1, wherein the natural polymer forms in water COO−anions and NH3±cations with at least 1×10−3 moles COOH/g and at least 0.5×10−3 moles NH2/g with an isoelectric point not less than 2.5 and not more than 10.5. 15. The method of claim 2, wherein the natural polymer is selected from the group consisting of collagen, atelocollagen, solubilized collagen, gelatin, collagen hydrolysate, alpha-keratose, gamma-keratose, keratin hydrolysate, elastin and derivatives, fibrin, fibroin, ovalbumin, bovine serum albumin, casein, soybean protein and derivatives of any of the foregoing polymers. 16. The method of claim 2, wherein the natural polymer is gelatin. 17. The method of claim 2, wherein the natural polymer is chemically modified by acylation reaction using a modifying agent selected from anhydrides and acid chlorides. 18. The method of claim 17, wherein the modifying agent is selected from the group consisting of phthalic anhydride, maleic anhydride, citraconic anhydride, itaconic anhydride, succinic anhydride, benzoyl chloride, benzenesulfonyl choride and butyryl chloride. 19. The method of claim 1, wherein R includes a spacer group interposed between the chemical function and the chain that is anchored to it. 20. The method of claim 19, wherein the spacer group is selected from —CO—0— and —(CH2)n— where n equals 1-4. 21. The method of claim 1, wherein the reactive chemical functions of synthetic polymer B, are chemical functions Rr , selected from —CO—O—CO— and —CO—NHCO—. 22. The method of claim 21, wherein the reactive chemical function is selected from maleic anhydride, itaconic anhydride, citraconic anhydride, 2-octenylsuccinic anhydride and corresponding imides. 23. The method of claim 1, wherein the ionic reactive chemical functionality of polymer B, is symbolized as frB, and is not less than 5×10−3 moles “r”/g and not more than 1×10−2 moles “r”/g. 24. The method of claim 1, wherein the non-reactive chemical functions Rncan comprise 1 to 4 groups selected from hydrogen, aliphatic or aromatic hydrocarbon residues with 1 to 20 carbon atoms, non-active ester, ether, or imino groups and nonactive halogen derivatives. 25. The method of claim 1, wherein the synthetic polymer B is prepared from monomers comprising monomers with non-reactive groups, selected from the group consisting of styrene, alpha-methyl styrene, alkylated styrenes, vinyl-toluene, vinyl esters of saturated C1-C4-carboxylic acids, alkyl vinyl ethers with at least 2 carbon atoms in the alkyl group, acrylate esters, methacrylate esters; conjugated diolefins; allenes; olefin halides, ethylene, propene, isobutylene, butadiene, isoprene, esters of monoethylenically unsaturated C3-C6-carboxylic acids, N-vinyllactams, acrylic and methacrylic esters of alkoxylated monohydric saturated alcohols, vinyl pyridine and vinyl morpholine, N-vinylformamide, dialkyldiallylammonium halides, N-vinylimidazoles, N-vinylimidazolines, acrylamide, methacrylamide and acrylonitrile. 26. The method of claim 25, wherein the monomers with non-reactive groups are selected from the group consisting of ethylene, propene, styrene, isobutylene, vinyl acetate, methyl acrylate, methyl methacrylate, acrylamide, vinylether, N-vinylpyrrolidone, acrylic acid, methacrylic acid and maleic acid. 27. The method of claim 25, wherein the synthetic polymer B is selected from poly (ethylene-alt-maleic anhydride), poly(ethylene-graft-maleic anhydride), poly(isobutylene-co-maleic anhydride), poly(isoprene-graft-maleic anhydride), poly(maleic anhydride-co-1-octadecene), polypropylene-graft-maleic anhydride), and poly(styrene-co-maleic anhydride).
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