JPS6341541A - 表面にキトサン成分を有する高分子成形物及びその製造方法 - Google Patents

表面にキトサン成分を有する高分子成形物及びその製造方法

Info

Publication number: JPS6341541A
Authority: JP; Japan
Prior art keywords: chitosan; high polymer; component; molded high; chitosan component
Prior art date: 1986-08-07
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.): Granted

Application number

JP61185805A

Other languages

English (en)

Japanese (ja)

Other versions

JPH0369374B2 (2

Inventor

Seiichi Aiba

誠一相羽

Norihiko Minoura

憲彦箕浦

Kazuhiro Taguchi

和宏田口

Yukihiko Fujiwara

冨士原　行彦

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

National Institute of Advanced Industrial Science and Technology AIST

Original Assignee

Agency of Industrial Science and Technology

Priority date (The priority date 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 date listed.)

1986-08-07

Filing date

1986-08-07

Publication date

1988-02-22

1986-08-07 Application filed by Agency of Industrial Science and Technology filed Critical Agency of Industrial Science and Technology

1986-08-07 Priority to JP61185805A priority Critical patent/JPS6341541A/ja

1988-02-22 Publication of JPS6341541A publication Critical patent/JPS6341541A/ja

1991-10-31 Publication of JPH0369374B2 publication Critical patent/JPH0369374B2/ja

Status Granted legal-status Critical Current

Links

229920001661 Chitosan Polymers 0.000 title claims abstract description 78
229920000642 polymer Polymers 0.000 title claims abstract description 26
238000000465 moulding Methods 0.000 claims 3
125000003277 amino group Chemical group 0.000 abstract description 15
239000003153 chemical reaction reagent Substances 0.000 abstract description 15
239000000243 solution Substances 0.000 abstract description 13
-1 polyethylene Polymers 0.000 abstract description 12
239000011248 coating agent Substances 0.000 abstract description 9
238000000576 coating method Methods 0.000 abstract description 9
150000001875 compounds Chemical class 0.000 abstract description 9
239000007864 aqueous solution Substances 0.000 abstract description 6
HZVOZRGWRWCICA-UHFFFAOYSA-N methanediyl Chemical compound [CH2] HZVOZRGWRWCICA-UHFFFAOYSA-N 0.000 abstract description 5
239000002253 acid Substances 0.000 abstract description 4
IVRMZWNICZWHMI-UHFFFAOYSA-N azide group Chemical group [N-]=[N+]=[N-] IVRMZWNICZWHMI-UHFFFAOYSA-N 0.000 abstract description 4
239000002473 artificial blood Substances 0.000 abstract description 3
210000004204 blood vessel Anatomy 0.000 abstract description 3
125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 abstract description 3
239000004698 Polyethylene Substances 0.000 abstract description 2
238000004113 cell culture Methods 0.000 abstract description 2
230000003100 immobilizing effect Effects 0.000 abstract description 2
229920000573 polyethylene Polymers 0.000 abstract description 2
239000000126 substance Substances 0.000 abstract description 2
239000000835 fiber Substances 0.000 abstract 1
239000000306 component Substances 0.000 description 27
239000000047 product Substances 0.000 description 26
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 21
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 21
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 18
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 15
239000000203 mixture Substances 0.000 description 12
238000010521 absorption reaction Methods 0.000 description 11
238000006243 chemical reaction Methods 0.000 description 11
125000002887 hydroxy group Chemical group [H]O* 0.000 description 10
WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 9
239000003795 chemical substances by application Substances 0.000 description 9
238000000862 absorption spectrum Methods 0.000 description 8
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 6
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
239000001257 hydrogen Substances 0.000 description 6
229910052739 hydrogen Inorganic materials 0.000 description 6
239000007788 liquid Substances 0.000 description 6
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
235000011121 sodium hydroxide Nutrition 0.000 description 6
239000011550 stock solution Substances 0.000 description 6
MSWZFWKMSRAUBD-IVMDWMLBSA-N 2-amino-2-deoxy-D-glucopyranose Chemical compound N[C@H]1C(O)O[C@H](CO)[C@@H](O)[C@@H]1O MSWZFWKMSRAUBD-IVMDWMLBSA-N 0.000 description 5
239000004372 Polyvinyl alcohol Substances 0.000 description 5
235000011054 acetic acid Nutrition 0.000 description 5
238000000034 method Methods 0.000 description 5
229920002451 polyvinyl alcohol Polymers 0.000 description 5
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
229920002683 Glycosaminoglycan Polymers 0.000 description 4
230000002378 acidificating effect Effects 0.000 description 4
150000001299 aldehydes Chemical class 0.000 description 4
238000001035 drying Methods 0.000 description 4
238000005406 washing Methods 0.000 description 4
KEQGZUUPPQEDPF-UHFFFAOYSA-N 1,3-dichloro-5,5-dimethylimidazolidine-2,4-dione Chemical compound CC1(C)N(Cl)C(=O)N(Cl)C1=O KEQGZUUPPQEDPF-UHFFFAOYSA-N 0.000 description 3
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
XTHPWXDJESJLNJ-UHFFFAOYSA-N chlorosulfonic acid Substances OS(Cl)(=O)=O XTHPWXDJESJLNJ-UHFFFAOYSA-N 0.000 description 3
238000006713 insertion reaction Methods 0.000 description 3
QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 3
229910052753 mercury Inorganic materials 0.000 description 3
230000000865 phosphorylative effect Effects 0.000 description 3
229920000468 styrene butadiene styrene block copolymer Polymers 0.000 description 3
238000005211 surface analysis Methods 0.000 description 3
RGHHSNMVTDWUBI-UHFFFAOYSA-N 4-hydroxybenzaldehyde Chemical compound OC1=CC=C(C=O)C=C1 RGHHSNMVTDWUBI-UHFFFAOYSA-N 0.000 description 2
HGINCPLSRVDWNT-UHFFFAOYSA-N Acrolein Chemical compound C=CC=O HGINCPLSRVDWNT-UHFFFAOYSA-N 0.000 description 2
229920002101 Chitin Polymers 0.000 description 2
241000238557 Decapoda Species 0.000 description 2
HTTJABKRGRZYRN-UHFFFAOYSA-N Heparin Chemical compound OC1C(NC(=O)C)C(O)OC(COS(O)(=O)=O)C1OC1C(OS(O)(=O)=O)C(O)C(OC2C(C(OS(O)(=O)=O)C(OC3C(C(O)C(O)C(O3)C(O)=O)OS(O)(=O)=O)C(CO)O2)NS(O)(=O)=O)C(C(O)=O)O1 HTTJABKRGRZYRN-UHFFFAOYSA-N 0.000 description 2
OVRNDRQMDRJTHS-FMDGEEDCSA-N N-acetyl-beta-D-glucosamine Chemical compound CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O OVRNDRQMDRJTHS-FMDGEEDCSA-N 0.000 description 2
239000004793 Polystyrene Substances 0.000 description 2
239000003513 alkali Substances 0.000 description 2
150000008064 anhydrides Chemical class 0.000 description 2
HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 description 2
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
MSWZFWKMSRAUBD-UHFFFAOYSA-N beta-D-galactosamine Natural products NC1C(O)OC(CO)C(O)C1O MSWZFWKMSRAUBD-UHFFFAOYSA-N 0.000 description 2
MSWZFWKMSRAUBD-QZABAPFNSA-N beta-D-glucosamine Chemical group N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O MSWZFWKMSRAUBD-QZABAPFNSA-N 0.000 description 2
239000004202 carbamide Substances 0.000 description 2
238000005266 casting Methods 0.000 description 2
229920001577 copolymer Polymers 0.000 description 2
XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
230000000694 effects Effects 0.000 description 2
150000002148 esters Chemical class 0.000 description 2
239000005038 ethylene vinyl acetate Substances 0.000 description 2
229920000669 heparin Polymers 0.000 description 2
229960002897 heparin Drugs 0.000 description 2
230000007062 hydrolysis Effects 0.000 description 2
238000006460 hydrolysis reaction Methods 0.000 description 2
230000001678 irradiating effect Effects 0.000 description 2
239000012948 isocyanate Substances 0.000 description 2
150000002513 isocyanates Chemical class 0.000 description 2
JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
239000000463 material Substances 0.000 description 2
BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
230000004048 modification Effects 0.000 description 2
238000012986 modification Methods 0.000 description 2
150000007524 organic acids Chemical class 0.000 description 2
ZRSNZINYAWTAHE-UHFFFAOYSA-N p-methoxybenzaldehyde Chemical compound COC1=CC=C(C=O)C=C1 ZRSNZINYAWTAHE-UHFFFAOYSA-N 0.000 description 2
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 2
229920002589 poly(vinylethylene) polymer Polymers 0.000 description 2
229920000867 polyelectrolyte Polymers 0.000 description 2
239000005518 polymer electrolyte Substances 0.000 description 2
239000002861 polymer material Substances 0.000 description 2
229920002223 polystyrene Polymers 0.000 description 2
QAOWNCQODCNURD-UHFFFAOYSA-L sulfate group Chemical group S(=O)(=O)([O-])[O-] QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
KIUKXJAPPMFGSW-DNGZLQJQSA-N (2S,3S,4S,5R,6R)-6-[(2S,3R,4R,5S,6R)-3-Acetamido-2-[(2S,3S,4R,5R,6R)-6-[(2R,3R,4R,5S,6R)-3-acetamido-2,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-2-carboxy-4,5-dihydroxyoxan-3-yl]oxy-5-hydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid Chemical compound CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@H](O[C@H]2[C@@H]([C@@H](O[C@H]3[C@@H]([C@@H](O)[C@H](O)[C@H](O3)C(O)=O)O)[C@H](O)[C@@H](CO)O2)NC(C)=O)[C@@H](C(O)=O)O1 KIUKXJAPPMFGSW-DNGZLQJQSA-N 0.000 description 1
OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
MGGVALXERJRIRO-UHFFFAOYSA-N 4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]-2-[2-oxo-2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethyl]-1H-pyrazol-5-one Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C=1C(=NN(C=1)CC(=O)N1CC2=C(CC1)NN=N2)O MGGVALXERJRIRO-UHFFFAOYSA-N 0.000 description 1
VCTBSHQJICJJFV-UHFFFAOYSA-N 4-azido-1-fluoro-2-nitrobenzene Chemical compound [O-][N+](=O)C1=CC(N=[N+]=[N-])=CC=C1F VCTBSHQJICJJFV-UHFFFAOYSA-N 0.000 description 1
SQDAZGGFXASXDW-UHFFFAOYSA-N 5-bromo-2-(trifluoromethoxy)pyridine Chemical compound FC(F)(F)OC1=CC=C(Br)C=N1 SQDAZGGFXASXDW-UHFFFAOYSA-N 0.000 description 1
238000004483 ATR-FTIR spectroscopy Methods 0.000 description 1
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
239000005711 Benzoic acid Substances 0.000 description 1
229920001287 Chondroitin sulfate Polymers 0.000 description 1
241000238424 Crustacea Species 0.000 description 1
SXRSQZLOMIGNAQ-UHFFFAOYSA-N Glutaraldehyde Chemical compound O=CCCCC=O SXRSQZLOMIGNAQ-UHFFFAOYSA-N 0.000 description 1
229920002971 Heparan sulfate Polymers 0.000 description 1
OHJKXVLJWUPWQG-PNRHKHKDSA-N Heparinsodiumsalt Chemical compound O[C@@H]1[C@@H](NS(O)(=O)=O)[C@@H](O)O[C@H](COS(O)(=O)=O)[C@H]1O[C@H]1[C@H](OS(O)(=O)=O)[C@@H](O)[C@H](O)[C@H](C(O)=O)O1 OHJKXVLJWUPWQG-PNRHKHKDSA-N 0.000 description 1
125000003047 N-acetyl group Chemical group 0.000 description 1
229920000459 Nitrile rubber Polymers 0.000 description 1
239000004952 Polyamide Substances 0.000 description 1
239000005062 Polybutadiene Substances 0.000 description 1
239000004743 Polypropylene Substances 0.000 description 1
241001125046 Sardina pilchardus Species 0.000 description 1
BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
IKHGUXGNUITLKF-XPULMUKRSA-N acetaldehyde Chemical compound [14CH]([14CH3])=O IKHGUXGNUITLKF-XPULMUKRSA-N 0.000 description 1
230000021736 acetylation Effects 0.000 description 1
238000006640 acetylation reaction Methods 0.000 description 1
150000008065 acid anhydrides Chemical class 0.000 description 1
239000011260 aqueous acid Substances 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
239000012298 atmosphere Substances 0.000 description 1
150000001540 azides Chemical group 0.000 description 1
235000010233 benzoic acid Nutrition 0.000 description 1
MSWZFWKMSRAUBD-YDMGZANHSA-N beta-D-Glucosamine Natural products N[C@H]1[C@H](O)O[C@@H](CO)[C@@H](O)[C@@H]1O MSWZFWKMSRAUBD-YDMGZANHSA-N 0.000 description 1
239000012620 biological material Substances 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
239000012503 blood component Substances 0.000 description 1
150000001649 bromium compounds Chemical class 0.000 description 1
150000001722 carbon compounds Chemical class 0.000 description 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
239000000969 carrier Substances 0.000 description 1
150000001805 chlorine compounds Chemical class 0.000 description 1
229940059329 chondroitin sulfate Drugs 0.000 description 1
229940004830 chondroitin sulfate a sodium Drugs 0.000 description 1
239000000470 constituent Substances 0.000 description 1
238000001514 detection method Methods 0.000 description 1
229910001873 dinitrogen Inorganic materials 0.000 description 1
YWEUIGNSBFLMFL-UHFFFAOYSA-N diphosphonate Chemical compound O=P(=O)OP(=O)=O YWEUIGNSBFLMFL-UHFFFAOYSA-N 0.000 description 1
238000007598 dipping method Methods 0.000 description 1
238000010828 elution Methods 0.000 description 1
239000004744 fabric Substances 0.000 description 1
235000019253 formic acid Nutrition 0.000 description 1
238000001641 gel filtration chromatography Methods 0.000 description 1
229960002442 glucosamine Drugs 0.000 description 1
150000004676 glycans Chemical class 0.000 description 1
150000004820 halides Chemical class 0.000 description 1
229920002674 hyaluronan Polymers 0.000 description 1
229960003160 hyaluronic acid Drugs 0.000 description 1
229920001477 hydrophilic polymer Polymers 0.000 description 1
239000011261 inert gas Substances 0.000 description 1
150000002561 ketenes Chemical class 0.000 description 1
239000004310 lactic acid Substances 0.000 description 1
235000014655 lactic acid Nutrition 0.000 description 1
WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
239000011259 mixed solution Substances 0.000 description 1
229910017464 nitrogen compound Inorganic materials 0.000 description 1
150000002830 nitrogen compounds Chemical class 0.000 description 1
210000000056 organ Anatomy 0.000 description 1
235000005985 organic acids Nutrition 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 description 1
DGTNSSLYPYDJGL-UHFFFAOYSA-N phenyl isocyanate Chemical compound O=C=NC1=CC=CC=C1 DGTNSSLYPYDJGL-UHFFFAOYSA-N 0.000 description 1
150000003014 phosphoric acid esters Chemical class 0.000 description 1
DLYUQMMRRRQYAE-UHFFFAOYSA-N phosphorus pentoxide Inorganic materials O1P(O2)(=O)OP3(=O)OP1(=O)OP2(=O)O3 DLYUQMMRRRQYAE-UHFFFAOYSA-N 0.000 description 1
230000026731 phosphorylation Effects 0.000 description 1
238000006366 phosphorylation reaction Methods 0.000 description 1
229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
229920002239 polyacrylonitrile Polymers 0.000 description 1
229920002647 polyamide Polymers 0.000 description 1
229920002857 polybutadiene Polymers 0.000 description 1
229920000728 polyester Polymers 0.000 description 1
238000006116 polymerization reaction Methods 0.000 description 1
239000004926 polymethyl methacrylate Substances 0.000 description 1
229920001155 polypropylene Polymers 0.000 description 1
229920001282 polysaccharide Polymers 0.000 description 1
239000005017 polysaccharide Substances 0.000 description 1
235000019260 propionic acid Nutrition 0.000 description 1
IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
239000012070 reactive reagent Substances 0.000 description 1
239000012266 salt solution Substances 0.000 description 1
235000019512 sardine Nutrition 0.000 description 1
238000000926 separation method Methods 0.000 description 1
229920002379 silicone rubber Polymers 0.000 description 1
239000004945 silicone rubber Substances 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
239000007921 spray Substances 0.000 description 1
239000006228 supernatant Substances 0.000 description 1
238000013269 sustained drug release Methods 0.000 description 1
230000002792 vascular Effects 0.000 description 1
229910052724 xenon Inorganic materials 0.000 description 1
FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 1

Landscapes

Treatments Of Macromolecular Shaped Articles (AREA)
Micro-Organisms Or Cultivation Processes Thereof (AREA)

JP61185805A 1986-08-07 1986-08-07 表面にキトサン成分を有する高分子成形物及びその製造方法 Granted JPS6341541A (ja)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
JP61185805A JPS6341541A (ja)	1986-08-07	1986-08-07	表面にキトサン成分を有する高分子成形物及びその製造方法

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP61185805A JPS6341541A (ja)	1986-08-07	1986-08-07	表面にキトサン成分を有する高分子成形物及びその製造方法

Publications (2)

Publication Number	Publication Date
JPS6341541A true JPS6341541A (ja)	1988-02-22
JPH0369374B2 JPH0369374B2 (2)	1991-10-31

Family

ID=16177196

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP61185805A Granted JPS6341541A (ja)	1986-08-07	1986-08-07	表面にキトサン成分を有する高分子成形物及びその製造方法

Country Status (1)

Country	Link
JP (1)	JPS6341541A (2)

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US5240747A (en) *	1989-05-11	1993-08-31	Kanegafuchi Kagaku Kogyo Kabushiki Kaisha	Process for modifying surfaces of materials
GB2371304A (en) *	2001-01-16	2002-07-24	Suisse Electronique Microtech	Surface passivation of organic polymers and elastomers
EP1227120A2 (en)	2001-01-24	2002-07-31	Novartis AG	Process for modifying a surface
US6730366B2 (en)	2001-01-24	2004-05-04	Novartis Ag	Process for modifying a surface
JP2010511375A (ja) *	2005-12-01	2010-04-15	エイジェンシーフォーサイエンス，テクノロジーアンドリサーチ	組織工学の足場としての三次元再構成細胞外マトリクス
JP2014527476A (ja) *	2011-07-18	2014-10-16	セルガードエルエルシー	表面修飾ポリマー材料及びこれを備えた電池セパレータ
CN105189625A (zh) *	2013-01-18	2015-12-23	赛尔格有限责任公司	表面改性剂、改性材料和方法
JP2020105490A (ja) *	2018-11-07	2020-07-09	国立大学法人東京大学	極性基含有オレフィン共重合体、及び極性基含有オレフィン共重合体組成物
JP2020105489A (ja) *	2018-11-07	2020-07-09	国立大学法人東京大学	極性基含有オレフィン重合体の製造方法
CN112175106A (zh) *	2020-10-13	2021-01-05	湖南洋韬材料科技有限公司	一种高活性叠氮壳聚糖抗菌剂及其制备方法
CN112194814A (zh) *	2020-10-13	2021-01-08	湖南洋韬材料科技有限公司	一种医用聚氨酯叠氮抗菌改性方法

1986
- 1986-08-07 JP JP61185805A patent/JPS6341541A/ja active Granted

Cited By (29)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US5240747A (en) *	1989-05-11	1993-08-31	Kanegafuchi Kagaku Kogyo Kabushiki Kaisha	Process for modifying surfaces of materials
GB2371304A (en) *	2001-01-16	2002-07-24	Suisse Electronique Microtech	Surface passivation of organic polymers and elastomers
EP1227120A2 (en)	2001-01-24	2002-07-31	Novartis AG	Process for modifying a surface
EP1227120A3 (en) *	2001-01-24	2003-08-27	Novartis AG	Process for modifying a surface
US6730366B2 (en)	2001-01-24	2004-05-04	Novartis Ag	Process for modifying a surface
JP2010511375A (ja) *	2005-12-01	2010-04-15	エイジェンシーフォーサイエンス，テクノロジーアンドリサーチ	組織工学の足場としての三次元再構成細胞外マトリクス
JP2014527476A (ja) *	2011-07-18	2014-10-16	セルガードエルエルシー	表面修飾ポリマー材料及びこれを備えた電池セパレータ
JP2023181408A (ja) *	2011-07-18	2023-12-21	セルガードエルエルシー	化学修飾基材
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