序号 专利名 申请号 申请日 公开(公告)号 公开(公告)日 发明人
201 Lili - to control Deibaisu JP15389884 1984-07-23 JPH0649644B2 1994-06-29 デビツト・アンソニー・ウツド; ニール・ボネツト・グラハム; マリオン・アイリーン・マクニール
202 JPH05505410A - JP51218290 1990-08-14 JPH05505410A 1993-08-12
203 Protein non-adsorptive polyurea-urethane polymer coated device JP7874092 1992-03-02 JPH05103831A 1993-04-27 JIEIMUZU ANSONII BURAATSU; AARON HAAMAN HEIFUETSUTSU; KURIFUTON RIROI KAA; RICHIYAADO ARAN URUFU
PURPOSE: To provide a medical and laboratory device which is coated with a polymer characterized by adaptability to vital organism and a resistance against non-peculiar protein adsorption. CONSTITUTION: A device according to the invention is coated with prepolymers whose terminals are capped with a high molecular weight isocyanate consisting of ethylene oxide unit sustantially or exclusively. The portion at least 75%, preferably over 90%, of the prepolymer unit should be diols or polyols including oxyethylene as radicals having a molecular weight of approx. 7000-30,000 where substantially all hydroxyl groups are capped with polyisocyanate prior to the manufacture of a hydrated polymer coating. COPYRIGHT: (C)1993,JPO
204 JPH0514586B2 - JP50156983 1983-05-06 JPH0514586B2 1993-02-25 HOOTAA UIRIAMU DANKAN; KIAMIRU SHINAAN BEHAEDEIN; HOWAITO NIKORASU DEIBITSUDO
205 Vinylic macromer, polymer and copolymer containing perfluoropolyalkyl ether and polyalkyl ether segment and ophthalmic device prepared of it JP440590 1990-01-11 JPH02258834A 1990-10-19 MERIRU GOORUDENBAAGU
PURPOSE: To obtain a macromer contg. specified perfluoroalkyl ether, polyalkyl ether segment and ethylenic unsatd. part and being suitable for flexible hydrogel contact lens. CONSTITUTION: A macromer contg. a perfluoropolyalkyl ether of formula I, [wherein Z is formula II (wherein a is 1-4 and b is 2-200); X is a direct bonding, -CH 2, carbonyl, etc.; Q is a direct bonding and -CONH-R-NHCO (wherein R is 2-14C divalent aliph. group, etc.); L is formula III (wherein Y is H and a direct bonding; m is 2-4; n is 5-100; A is oxa and imino); T is -CONH-R 5A- (wherein R 5 is a 2-15C alkylene); E is -CO-C(R 1)=CHR 2 (wherein R 1 and R 2 are each H, CH 3, etc.)], formula IV, formula V and formula VI, polyalkyl ether segment and ethylenic unsatd. part, is provided. COPYRIGHT: (C)1990,JPO
206 Chemically modified hydrophilic prepolymer and polymer JP28316389 1989-11-01 JPH02209915A 1990-08-21 JIEIMUZU ANSONII BURAATSU; AARON HAAMAN HAIFUETSUTSU; RICHIYAADO ARAN URUFU; NARENDAA PARU RUUSURA
PURPOSE: To obtain a prepolymer which is hydrophilic, biocompatible, capable of the reversible formation of a hydrogel, the enhancement of cell growth, etc., and desirable for e.g. biomedical use by modifying a specified NCO- terminated prepolymer with a specified compound. CONSTITUTION: This prepolymer is obtained by modifying an NCOterminated prepolymer which has prepolymer units each of which is derived from an oxyethylene-based alcohol and in which all of the hydroxyl groups are blocked with a polyisocyanate with a compound (A) having an NCO-reactive first functional group comprising a sulfhydryl, OH or an amino contained in a monoamine compound and a second functional group less NCO-reactive than the first functional group (e.g. 2-aminoethanol) or a compound (B) having a first functional group comprising COOH or an amino group contained in a polyamine compound or the like and being capable of modifying all of the NCO groups of the prepolymer and having a second functional group less NCO-reactive than the first functional group. COPYRIGHT: (C)1990,JPO
207 JPH01501287A - JP50537087 1987-09-21 JPH01501287A 1989-05-11
208 Grout composition JP21362785 1985-09-26 JPS6195087A 1986-05-13 ARUTON JIYOSEFU GASUPAA; CHIYAARUZU DEIIN RAITO
A grouting composition for sealing structures to inhibit water leakage therethrough and for stabilizing soil is provided. The composition is provided as a two-part system. Part A is an aqueous solution of a hydrophilic, water soluble prepolymer having a polyether backbone and terminal active olefinic groups, the olefinic groups being connected to the polyether backbone by linking groups selected from -NH-, -CONH-, -OCONH-, and -NHCONH-, and tertiary amine catalyst. Part B is an aqueous solution of a peroxy initiator. Parts A and B are mixed and react to form a gel.
209 Method of bridgeing polyalkylene polyamine and manufacture of foamed body JP4033985 1985-03-02 JPS61217A 1986-01-06 HARORUDO EICHI FURIIDOMAN
210 Release control device JP15389884 1984-07-23 JPS6042321A 1985-03-06 NIIRU BONETSUTO GURAHAMU; MARION AIRIIN MAKUNIIRU; DEBITSUTO ANSONII UTSUDO
211 JPS59500751A - JP50156983 1983-05-06 JPS59500751A 1984-05-04
212 Hydrogel modified membrane, manufacture and use as active reagent dispenser JP11236381 1981-07-20 JPS5755967A 1982-04-03 KAARU FURIIDORITSUHI MIYUURAA; SONIA JIYAUORIU HAIBAA
213 JPS56500253A - JP50062480 1980-03-21 JPS56500253A 1981-03-05
214 Fireeproofing polyurethane gel composition* its manufacture and its use JP2745180 1980-03-06 JPS55120621A 1980-09-17 RUISU REONAADO UTSUDO; GUREN ERUTON FURUMAA
A fire-retardant protective coating is produced by dissolving a water-soluble polyisocyanate prepolymer in either an aqueous slurry or solution of fire-retardant materials and/or intumescent materials. After mixing, the gel produced can be applied as a coating which is useful for protecting or holding together surfaces vulnerable to fire, heat, air or minor abrasion. After the water evaporates, the cross-linked polyurethane coating has a large solids content of the fire-retardant and/or intumescent materials uniformly dispersed throughout. Preferred prepolymers are liquid with a molecular weight greater than about 2,000 and are made of a random copolymer of ethylene oxide and other alkylene oxides with isocyanate capping.
215 GEL COMPOSITION US15559743 2017-06-15 US20180346847A1 2018-12-06 Natsu FUKUDA; Masatake JOYABU
A gel composition having high adhesion, high whitening resistance, and high high-temperature stability is provided.The gel composition includes a polyoxyalkylene alkyl ether (A) represented by general formula (1) and water (B). R—O—(PO)m-(EO)n—H   (1) In the formula (1), R is a linear alkyl group having 12 to 22 carbon atoms, PO represents an oxypropylene group, EO represents an oxyethylene group, m and n each represent an average number of moles added, m is a number of 1 to 20, and n is a number of 1 to 80. PO and EO are added in a configuration of block addition.
216 THERMOFORMABLE DUAL NETWORK HYDROGEL COMPOSITIONS US15773643 2016-11-02 US20180311358A1 2018-11-01 Nancy S. Marchant; James R. Baxter; William A. Stansbrey
A thermoformable dual network hydrogel composition formed from a cross-linked polymer derived from one or more olefinically unsaturated polymerizable carboxylic monomers and one or more thermoplastic polyurethane compositions is disclosed. The hydrogel exhibits high elastic modulus and Yield Stress at low shear, and a moderate but significant adhesion force. The hydrogel composition provides useful materials for personal care, health care, medical and pharmaceutical applications, among others.
217 Bone repair material US15476012 2017-03-31 US10098983B2 2018-10-16 Corinna Mauth; Aaldert-Rens Molenberg
Sliceable bone repair material is a porous block-shaped scaffold containing a hydrogel, wherein the hydrogel is formed by Michael type addition of at least two precursor molecules. Said scaffold is made of a synthetic ceramic material and has interconnected macropores having a diameter above 100 μm. In addition said scaffold has a total porosity of 80 to 95%. The total volume of the hydrogel is smaller than the total volume of the interconnected macropores.
218 METHOD FOR PREPARING SUPERABSORBENT POLYMER US15506828 2015-12-14 US20180257059A1 2018-09-13 Seong Beom HEO; Tae Hwan JANG; Mi Young KIM; Jiyoon JEONG; Bhom Ri KIM
The preparation method of superabsorbent polymer according to the present invention can increase suction power without degradation of other properties of superabsorbent polymer, and thus, the prepared superabsorbent polymer may be usefully used as material of hygienic goods such as a diaper.
219 Method for producing hydrogel, method for enveloping envelopment target, and method for releasing envelopment target US15304675 2015-04-16 US10016506B2 2018-07-10 Noriho Kamiya; Kosuke Moriyama; Kosuke Minamihata
Provided is a method for producing a hydrogel, which enables a hydrogel comprising polyethylene glycol to be produced under low peroxidase concentration conditions and physiological conditions. The method for producing a hydrogel involves crosslinking polyethylene glycol having two or more thiol groups using peroxidase in the presence of a phenol compound.
220 Vitamin functionalized gel-forming block copolymers for biomedical applications US15340795 2016-11-01 US09987369B2 2018-06-05 Wei Cheng; Mareva B. Fevre; James L. Hedrick; Nor Lizawati Ibrahim; Ashlynn L. Z. Lee; Victor W. L. Ng; Robert J. Ono; Chuan Yang; Yi Yan Yang
Gel-forming block copolymers were prepared comprising i) a central hydrophilic block consisting essentially of a divalent poly(ethylene oxide) chain and ii) two peripheral monocarbonate or polycarbonate hydrophobic blocks linked to the central block by linking groups bearing one or more hydrogen bond forming *—N(H)—* groups. The hydrophobic blocks comprise one or more vitamin-bearing subunits. The gel-forming block copolymers can be used to prepare various biodegradable and/or biocompatible hydrogel and organogel drug compositions, in particular antimicrobial and/or anti-tumor drug compositions. The hydrogel compositions have utility in depot injections for drug delivery. The hydrogen bonding *—N(H)—* group(s) provide longer in vivo lifetime of the hydrogel before degradation and a more prolonged and controlled release rate of a hydrophobic drug compared to similar hydrogels prepared from poly(ethylene glycol).
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