JP2009542856A - 重合可能なカチオン親水基でエンドキャップされたフッ素化ポリ（エーテル） - Google Patents
重合可能なカチオン親水基でエンドキャップされたフッ素化ポリ（エーテル） Download PDFInfo
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- JP2009542856A JP2009542856A JP2009518435A JP2009518435A JP2009542856A JP 2009542856 A JP2009542856 A JP 2009542856A JP 2009518435 A JP2009518435 A JP 2009518435A JP 2009518435 A JP2009518435 A JP 2009518435A JP 2009542856 A JP2009542856 A JP 2009542856A
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- 125000004619 benzopyranyl group Chemical group O1C(C=CC2=C1C=CC=C2)* 0.000 description 1
- 125000001164 benzothiazolyl group Chemical group S1C(=NC2=C1C=CC=C2)* 0.000 description 1
- 125000004196 benzothienyl group Chemical group S1C(=CC2=C1C=CC=C2)* 0.000 description 1
- 125000004541 benzoxazolyl group Chemical group O1C(=NC2=C1C=CC=C2)* 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 210000001124 body fluid Anatomy 0.000 description 1
- 239000010839 body fluid Substances 0.000 description 1
- 210000000988 bone and bone Anatomy 0.000 description 1
- 239000003618 borate buffered saline Substances 0.000 description 1
- 239000007853 buffer solution Substances 0.000 description 1
- 239000007975 buffered saline Substances 0.000 description 1
- 238000004364 calculation method Methods 0.000 description 1
- 150000004657 carbamic acid derivatives Chemical class 0.000 description 1
- 125000000609 carbazolyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3NC12)* 0.000 description 1
- 239000011203 carbon fibre reinforced carbon Substances 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
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- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 125000003016 chromanyl group Chemical group O1C(CCC2=CC=CC=C12)* 0.000 description 1
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- 125000002433 cyclopentenyl group Chemical group C1(=CCCC1)* 0.000 description 1
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- 125000000298 cyclopropenyl group Chemical group [H]C1=C([H])C1([H])* 0.000 description 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
- 125000004186 cyclopropylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C1([H])[H] 0.000 description 1
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- 125000005507 decahydroisoquinolyl group Chemical group 0.000 description 1
- 238000000502 dialysis Methods 0.000 description 1
- WZMKPWYXKROFBY-UHFFFAOYSA-N diazanium 2-methylprop-2-enoate bromide Chemical compound [Br-].[NH4+].C(C(=C)C)(=O)[O-].[NH4+] WZMKPWYXKROFBY-UHFFFAOYSA-N 0.000 description 1
- SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 description 1
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- 125000005879 dioxolanyl group Chemical group 0.000 description 1
- PYBNTRWJKQJDRE-UHFFFAOYSA-L dodecanoate;tin(2+) Chemical compound [Sn+2].CCCCCCCCCCCC([O-])=O.CCCCCCCCCCCC([O-])=O PYBNTRWJKQJDRE-UHFFFAOYSA-L 0.000 description 1
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- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- ZHPNWZCWUUJAJC-UHFFFAOYSA-N fluorosilicon Chemical compound [Si]F ZHPNWZCWUUJAJC-UHFFFAOYSA-N 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000012634 fragment Substances 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 125000002541 furyl group Chemical group 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 150000002357 guanidines Chemical class 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 125000002883 imidazolyl group Chemical group 0.000 description 1
- 125000003392 indanyl group Chemical group C1(CCC2=CC=CC=C12)* 0.000 description 1
- 125000003454 indenyl group Chemical group C1(C=CC2=CC=CC=C12)* 0.000 description 1
- 125000003387 indolinyl group Chemical group N1(CCC2=CC=CC=C12)* 0.000 description 1
- 125000003406 indolizinyl group Chemical group C=1(C=CN2C=CC=CC12)* 0.000 description 1
- 125000001041 indolyl group Chemical group 0.000 description 1
- 125000003010 ionic group Chemical group 0.000 description 1
- 230000007794 irritation Effects 0.000 description 1
- 125000003384 isochromanyl group Chemical group C1(OCCC2=CC=CC=C12)* 0.000 description 1
- 125000004594 isoindolinyl group Chemical group C1(NCC2=CC=CC=C12)* 0.000 description 1
- 125000000904 isoindolyl group Chemical group C=1(NC=C2C=CC=CC12)* 0.000 description 1
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- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
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- 150000002894 organic compounds Chemical class 0.000 description 1
- 125000005375 organosiloxane group Chemical group 0.000 description 1
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- 125000001791 phenazinyl group Chemical group C1(=CC=CC2=NC3=CC=CC=C3N=C12)* 0.000 description 1
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- 230000035479 physiological effects, processes and functions Effects 0.000 description 1
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- 238000005498 polishing Methods 0.000 description 1
- 229920000233 poly(alkylene oxides) Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920006254 polymer film Polymers 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 239000004810 polytetrafluoroethylene Substances 0.000 description 1
- 229920000166 polytrimethylene carbonate Polymers 0.000 description 1
- 125000001042 pteridinyl group Chemical group N1=C(N=CC2=NC=CN=C12)* 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000008213 purified water Substances 0.000 description 1
- 125000000561 purinyl group Chemical group N1=C(N=C2N=CNC2=C1)* 0.000 description 1
- 125000003373 pyrazinyl group Chemical group 0.000 description 1
- 125000002098 pyridazinyl group Chemical group 0.000 description 1
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- 125000000168 pyrrolyl group Chemical group 0.000 description 1
- 125000002294 quinazolinyl group Chemical group N1=C(N=CC2=CC=CC=C12)* 0.000 description 1
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- 125000001567 quinoxalinyl group Chemical group N1=C(C=NC2=CC=CC=C12)* 0.000 description 1
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- 125000003107 substituted aryl group Chemical group 0.000 description 1
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- 125000006090 thiamorpholinyl sulfone group Chemical group 0.000 description 1
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- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 125000001425 triazolyl group Chemical group 0.000 description 1
- 150000003673 urethanes Chemical class 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/32—Polymers modified by chemical after-treatment
- C08G65/329—Polymers modified by chemical after-treatment with organic compounds
- C08G65/333—Polymers modified by chemical after-treatment with organic compounds containing nitrogen
- C08G65/33303—Polymers modified by chemical after-treatment with organic compounds containing nitrogen containing amino group
- C08G65/33306—Polymers modified by chemical after-treatment with organic compounds containing nitrogen containing amino group acyclic
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/002—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from unsaturated compounds
- C08G65/005—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from unsaturated compounds containing halogens
- C08G65/007—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from unsaturated compounds containing halogens containing fluorine
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G2650/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G2650/28—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule characterised by the polymer type
- C08G2650/46—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule characterised by the polymer type containing halogen
- C08G2650/48—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule characterised by the polymer type containing halogen containing fluorine, e.g. perfluropolyethers
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Eyeglasses (AREA)
- Materials For Medical Uses (AREA)
- Macromonomer-Based Addition Polymer (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US11/480,170 US8105623B2 (en) | 2006-06-30 | 2006-06-30 | Fluorinated poly(ether)s end-capped with polymerizable cationic hydrophilic groups |
| PCT/US2007/070754 WO2008005652A1 (en) | 2006-06-30 | 2007-06-08 | Fluorinated poly (ether)s end-capped with polymerizable cationic hydrophilic groups |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2009542856A true JP2009542856A (ja) | 2009-12-03 |
| JP2009542856A5 JP2009542856A5 (enExample) | 2010-12-24 |
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| US (2) | US8105623B2 (enExample) |
| EP (1) | EP2035480B1 (enExample) |
| JP (1) | JP2009542856A (enExample) |
| CN (1) | CN101479318A (enExample) |
| AT (1) | ATE458020T1 (enExample) |
| DE (1) | DE602007004850D1 (enExample) |
| ES (1) | ES2339610T3 (enExample) |
| WO (1) | WO2008005652A1 (enExample) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
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| US8105623B2 (en) * | 2006-06-30 | 2012-01-31 | Bausch & Lomb Incorporated | Fluorinated poly(ether)s end-capped with polymerizable cationic hydrophilic groups |
| US9486311B2 (en) | 2013-02-14 | 2016-11-08 | Shifamed Holdings, Llc | Hydrophilic AIOL with bonding |
| AU2014236688B2 (en) | 2013-03-21 | 2019-07-25 | Shifamed Holdings, Llc | Accommodating intraocular lens |
| US10195018B2 (en) | 2013-03-21 | 2019-02-05 | Shifamed Holdings, Llc | Accommodating intraocular lens |
| AU2015306613B2 (en) | 2014-08-26 | 2018-01-25 | Shifamed Holdings, Llc | Accommodating intraocular lens |
| CN108472129B (zh) | 2015-11-18 | 2021-09-24 | 施菲姆德控股有限责任公司 | 组合的调节性人工晶状体 |
| US11141263B2 (en) | 2015-11-18 | 2021-10-12 | Shifamed Holdings, Llc | Multi-piece accommodating intraocular lens |
| KR101738306B1 (ko) | 2016-07-27 | 2017-06-09 | 포항공과대학교 산학협력단 | 플루오르카본이 도입된 비휘발성 메모리 특성 자기조립성 브러쉬 블록 공중합체, 이의 제조방법 및 이를 이용하는 메모리 소자 |
| WO2018029131A1 (en) * | 2016-08-09 | 2018-02-15 | Solvay Specialty Polymers Italy S.P.A. | Porous membranes |
| JP6954679B2 (ja) | 2016-12-23 | 2021-10-27 | シファメド・ホールディングス・エルエルシー | マルチピース調節式眼内レンズ、及び同を作成し、使用するための方法 |
| US10350056B2 (en) | 2016-12-23 | 2019-07-16 | Shifamed Holdings, Llc | Multi-piece accommodating intraocular lenses and methods for making and using same |
| KR101940281B1 (ko) * | 2017-03-21 | 2019-01-22 | 주식회사 쎄코 | 강유전성 브러쉬-고분자, 이를 이용한 강유전체 메모리 소자 및 이의 제조방법 |
| JP7370052B2 (ja) | 2017-05-30 | 2023-10-27 | シファメド・ホールディングス・エルエルシー | 調節眼内レンズのための表面処理ならびに関連する方法およびデバイス |
| JP7082822B2 (ja) | 2017-06-07 | 2022-06-09 | シファメド・ホールディングス・エルエルシー | 調整可能な屈折力の眼内レンズ |
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| JPS617312A (ja) * | 1984-06-22 | 1986-01-14 | Toyo Soda Mfg Co Ltd | フルオロカ−ボン重合体 |
| JPS6198708A (ja) * | 1984-06-22 | 1986-05-17 | Toyo Soda Mfg Co Ltd | 含フツ素アンモニウム型重合体 |
| JPH0667122A (ja) * | 1992-08-18 | 1994-03-11 | Nippon Oil & Fats Co Ltd | ソフトコンタクトレンズ |
| JPH10218988A (ja) * | 1997-02-07 | 1998-08-18 | Kao Corp | 反応型含フッ素ポリエーテル及びその製造方法 |
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| EP0379462B1 (en) | 1989-01-11 | 1995-02-22 | Ciba-Geigy Ag | Vinylic macromers containing perfluoropolyalkylether and polyalkylether segments, polymers, copolymers and ophthalmic devices made therefrom |
| US5070215A (en) | 1989-05-02 | 1991-12-03 | Bausch & Lomb Incorporated | Novel vinyl carbonate and vinyl carbamate contact lens material monomers |
| US5034461A (en) | 1989-06-07 | 1991-07-23 | Bausch & Lomb Incorporated | Novel prepolymers useful in biomedical devices |
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| US5374662A (en) | 1993-03-15 | 1994-12-20 | Bausch & Lomb Incorporated | Fumarate and fumaramide siloxane hydrogel compositions |
| US5451651A (en) | 1993-12-17 | 1995-09-19 | Bausch & Lomb Incorporated | Urea and urethane monomers for contact lens materials |
| US6306563B1 (en) * | 1999-06-21 | 2001-10-23 | Corning Inc. | Optical devices made from radiation curable fluorinated compositions |
| IT1318558B1 (it) * | 2000-06-08 | 2003-08-27 | Ausimont Spa | Poliuretani a basso coefficiente di attrito. |
| FR2848563B1 (fr) * | 2002-12-16 | 2006-07-28 | Rhodia Chimie Sa | Composition silicone pour revetement dur, a base de silice colloidale, durcissable par voie cationique, antibuee et/ou antisalissures |
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| US7622512B2 (en) | 2005-12-21 | 2009-11-24 | Bausch & Lomb Incorporated | Cationic hydrophilic siloxanyl monomers |
| US7528208B2 (en) | 2006-01-06 | 2009-05-05 | Bausch & Lomb Incorporated | Siloxane prepolymer containing pendant and end-capping cationic and polymerizable groups |
| US7557231B2 (en) | 2006-06-30 | 2009-07-07 | Bausch & Lomb Incorporated | Carboxylic tris-like siloxanyl monomers |
| US7601766B2 (en) | 2006-06-30 | 2009-10-13 | Bausch & Lomb Incorporated | Carboxylic siloxanyl monomers with pendant polymerizable groups |
| US8105623B2 (en) * | 2006-06-30 | 2012-01-31 | Bausch & Lomb Incorporated | Fluorinated poly(ether)s end-capped with polymerizable cationic hydrophilic groups |
| US7468397B2 (en) | 2006-06-30 | 2008-12-23 | Bausch & Lomb Incorporated | Polymerizable siloxane-quaternary amine copolymers |
| US7837934B2 (en) * | 2008-01-09 | 2010-11-23 | Bausch & Lomb Incorporated | Packaging solutions |
-
2006
- 2006-06-30 US US11/480,170 patent/US8105623B2/en not_active Expired - Fee Related
-
2007
- 2007-06-08 EP EP07798308A patent/EP2035480B1/en not_active Not-in-force
- 2007-06-08 AT AT07798308T patent/ATE458020T1/de not_active IP Right Cessation
- 2007-06-08 WO PCT/US2007/070754 patent/WO2008005652A1/en not_active Ceased
- 2007-06-08 DE DE602007004850T patent/DE602007004850D1/de active Active
- 2007-06-08 JP JP2009518435A patent/JP2009542856A/ja not_active Ceased
- 2007-06-08 CN CNA2007800236934A patent/CN101479318A/zh active Pending
- 2007-06-08 ES ES07798308T patent/ES2339610T3/es active Active
-
2011
- 2011-12-21 US US13/332,637 patent/US20120095177A1/en not_active Abandoned
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS4951384A (enExample) * | 1972-09-14 | 1974-05-18 | ||
| JPS6084313A (ja) * | 1983-10-17 | 1985-05-13 | Toyo Soda Mfg Co Ltd | アンモニウム型重合体及びその製造方法 |
| JPS617312A (ja) * | 1984-06-22 | 1986-01-14 | Toyo Soda Mfg Co Ltd | フルオロカ−ボン重合体 |
| JPS6198708A (ja) * | 1984-06-22 | 1986-05-17 | Toyo Soda Mfg Co Ltd | 含フツ素アンモニウム型重合体 |
| JPH0667122A (ja) * | 1992-08-18 | 1994-03-11 | Nippon Oil & Fats Co Ltd | ソフトコンタクトレンズ |
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| JPH10218988A (ja) * | 1997-02-07 | 1998-08-18 | Kao Corp | 反応型含フッ素ポリエーテル及びその製造方法 |
| JP2007526797A (ja) * | 2003-12-24 | 2007-09-20 | サインコア，リミテッド・ライアビリティ・カンパニー | 液体パーフルオロポリマーおよびこれを組み入れた医学的用途 |
Also Published As
| Publication number | Publication date |
|---|---|
| EP2035480A1 (en) | 2009-03-18 |
| US20120095177A1 (en) | 2012-04-19 |
| US20080003261A1 (en) | 2008-01-03 |
| CN101479318A (zh) | 2009-07-08 |
| US8105623B2 (en) | 2012-01-31 |
| EP2035480B1 (en) | 2010-02-17 |
| ES2339610T3 (es) | 2010-05-21 |
| DE602007004850D1 (de) | 2010-04-01 |
| ATE458020T1 (de) | 2010-03-15 |
| WO2008005652A1 (en) | 2008-01-10 |
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