IL101035A - Contact lenses made of thermally designed material - Google Patents

Contact lenses made of thermally designed material

Info

Publication number: IL101035A
Authority: IL; Israel
Prior art keywords: lower alkyl; contact lens; carbon atoms; alkylene; hydrogen
Prior art date: 1991-02-28

Application number

IL10103592A

Other languages

English (en)

Hebrew (he)

Other versions

IL101035A0 (en

Original Assignee

Ciba Geigy Ag

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.)

1991-02-28

Filing date

1992-02-21

Publication date

1995-06-29

1992-02-21 Application filed by Ciba Geigy Ag filed Critical Ciba Geigy Ag

1992-11-15 Publication of IL101035A0 publication Critical patent/IL101035A0/xx

1995-06-29 Publication of IL101035A publication Critical patent/IL101035A/en

Links

239000000463 material Substances 0.000 title claims description 11
125000000217 alkyl group Chemical group 0.000 claims abstract description 40
150000002678 macrocyclic compounds Chemical class 0.000 claims abstract description 36
125000004432 carbon atom Chemical group C* 0.000 claims abstract description 29
229920000642 polymer Polymers 0.000 claims abstract description 23
125000002947 alkylene group Chemical group 0.000 claims abstract description 21
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 18
239000001257 hydrogen Substances 0.000 claims abstract description 18
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 17
238000000748 compression moulding Methods 0.000 claims abstract description 15
125000004450 alkenylene group Chemical group 0.000 claims abstract description 8
-1 siloxane acrylates Chemical class 0.000 claims description 23
WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 claims description 15
239000000654 additive Substances 0.000 claims description 15
229920006217 cellulose acetate butyrate Polymers 0.000 claims description 12
239000003431 cross linking reagent Substances 0.000 claims description 12
239000000470 constituent Substances 0.000 claims description 10
229920000191 poly(N-vinyl pyrrolidone) Polymers 0.000 claims description 9
238000004519 manufacturing process Methods 0.000 claims description 7
238000000034 method Methods 0.000 claims description 7
150000001875 compounds Chemical class 0.000 claims description 6
150000002734 metacrylic acid derivatives Chemical class 0.000 claims description 6
239000002253 acid Substances 0.000 claims description 4
125000005250 alkyl acrylate group Chemical group 0.000 claims description 4
150000002148 esters Chemical class 0.000 claims description 4
229930195733 hydrocarbon Natural products 0.000 claims description 4
150000002430 hydrocarbons Chemical class 0.000 claims description 4
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 2
229910052731 fluorine Inorganic materials 0.000 claims description 2
239000011737 fluorine Substances 0.000 claims description 2
125000000524 functional group Chemical group 0.000 claims description 2
125000000623 heterocyclic group Chemical group 0.000 claims description 2
150000002433 hydrophilic molecules Chemical class 0.000 claims description 2
230000002209 hydrophobic effect Effects 0.000 claims description 2
125000004356 hydroxy functional group Chemical group O* 0.000 claims description 2
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 2
150000002431 hydrogen Chemical class 0.000 claims 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract description 7
229910052760 oxygen Inorganic materials 0.000 abstract description 7
239000001301 oxygen Substances 0.000 abstract description 7
230000035699 permeability Effects 0.000 abstract description 6
150000003254 radicals Chemical class 0.000 description 10
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 9
238000004132 cross linking Methods 0.000 description 7
238000000465 moulding Methods 0.000 description 5
229920003245 polyoctenamer Polymers 0.000 description 5
NOBYOEQUFMGXBP-UHFFFAOYSA-N (4-tert-butylcyclohexyl) (4-tert-butylcyclohexyl)oxycarbonyloxy carbonate Chemical compound C1CC(C(C)(C)C)CCC1OC(=O)OOC(=O)OC1CCC(C(C)(C)C)CC1 NOBYOEQUFMGXBP-UHFFFAOYSA-N 0.000 description 4
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
239000000243 solution Substances 0.000 description 4
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 3
238000001035 drying Methods 0.000 description 3
239000003999 initiator Substances 0.000 description 3
239000000203 mixture Substances 0.000 description 3
239000007858 starting material Substances 0.000 description 3
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 3
ZGEGCLOFRBLKSE-UHFFFAOYSA-N 1-Heptene Chemical group CCCCCC=C ZGEGCLOFRBLKSE-UHFFFAOYSA-N 0.000 description 2
BJELTSYBAHKXRW-UHFFFAOYSA-N 2,4,6-triallyloxy-1,3,5-triazine Chemical compound C=CCOC1=NC(OCC=C)=NC(OCC=C)=N1 BJELTSYBAHKXRW-UHFFFAOYSA-N 0.000 description 2
OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 2
XMNIXWIUMCBBBL-UHFFFAOYSA-N 2-(2-phenylpropan-2-ylperoxy)propan-2-ylbenzene Chemical compound C=1C=CC=CC=1C(C)(C)OOC(C)(C)C1=CC=CC=C1 XMNIXWIUMCBBBL-UHFFFAOYSA-N 0.000 description 2
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 2
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
230000006835 compression Effects 0.000 description 2
238000007906 compression Methods 0.000 description 2
ZQMIGQNCOMNODD-UHFFFAOYSA-N diacetyl peroxide Chemical compound CC(=O)OOC(C)=O ZQMIGQNCOMNODD-UHFFFAOYSA-N 0.000 description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
229920001519 homopolymer Polymers 0.000 description 2
238000005649 metathesis reaction Methods 0.000 description 2
229920003229 poly(methyl methacrylate) Polymers 0.000 description 2
239000004926 polymethyl methacrylate Substances 0.000 description 2
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
230000005855 radiation Effects 0.000 description 2
229910052710 silicon Inorganic materials 0.000 description 2
239000010703 silicon Substances 0.000 description 2
238000012360 testing method Methods 0.000 description 2
WRXCBRHBHGNNQA-UHFFFAOYSA-N (2,4-dichlorobenzoyl) 2,4-dichlorobenzenecarboperoxoate Chemical compound ClC1=CC(Cl)=CC=C1C(=O)OOC(=O)C1=CC=C(Cl)C=C1Cl WRXCBRHBHGNNQA-UHFFFAOYSA-N 0.000 description 1
HGXJDMCMYLEZMJ-UHFFFAOYSA-N (2-methylpropan-2-yl)oxy 2,2-dimethylpropaneperoxoate Chemical compound CC(C)(C)OOOC(=O)C(C)(C)C HGXJDMCMYLEZMJ-UHFFFAOYSA-N 0.000 description 1
KDGNCLDCOVTOCS-UHFFFAOYSA-N (2-methylpropan-2-yl)oxy propan-2-yl carbonate Chemical compound CC(C)OC(=O)OOC(C)(C)C KDGNCLDCOVTOCS-UHFFFAOYSA-N 0.000 description 1
OXYKVVLTXXXVRT-UHFFFAOYSA-N (4-chlorobenzoyl) 4-chlorobenzenecarboperoxoate Chemical compound C1=CC(Cl)=CC=C1C(=O)OOC(=O)C1=CC=C(Cl)C=C1 OXYKVVLTXXXVRT-UHFFFAOYSA-N 0.000 description 1
BLKRGXCGFRXRNQ-SNAWJCMRSA-N (z)-3-carbonoperoxoyl-4,4-dimethylpent-2-enoic acid Chemical compound OC(=O)/C=C(C(C)(C)C)\C(=O)OO BLKRGXCGFRXRNQ-SNAWJCMRSA-N 0.000 description 1
ZPOUDMYDJJMHOO-UHFFFAOYSA-N 1-(1-hydroxycyclohexyl)peroxycyclohexan-1-ol Chemical compound C1CCCCC1(O)OOC1(O)CCCCC1 ZPOUDMYDJJMHOO-UHFFFAOYSA-N 0.000 description 1
AFFLGGQVNFXPEV-UHFFFAOYSA-N 1-decene Chemical group CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 1
KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical group CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 1
PFHOSZAOXCYAGJ-UHFFFAOYSA-N 2-[(2-cyano-4-methoxy-4-methylpentan-2-yl)diazenyl]-4-methoxy-2,4-dimethylpentanenitrile Chemical compound COC(C)(C)CC(C)(C#N)N=NC(C)(C#N)CC(C)(C)OC PFHOSZAOXCYAGJ-UHFFFAOYSA-N 0.000 description 1
WYGWHHGCAGTUCH-UHFFFAOYSA-N 2-[(2-cyano-4-methylpentan-2-yl)diazenyl]-2,4-dimethylpentanenitrile Chemical compound CC(C)CC(C)(C#N)N=NC(C)(C#N)CC(C)C WYGWHHGCAGTUCH-UHFFFAOYSA-N 0.000 description 1
WFUGQJXVXHBTEM-UHFFFAOYSA-N 2-hydroperoxy-2-(2-hydroperoxybutan-2-ylperoxy)butane Chemical compound CCC(C)(OO)OOC(C)(CC)OO WFUGQJXVXHBTEM-UHFFFAOYSA-N 0.000 description 1
XYFRHHAYSXIKGH-UHFFFAOYSA-N 3-(5-methoxy-2-methoxycarbonyl-1h-indol-3-yl)prop-2-enoic acid Chemical compound C1=C(OC)C=C2C(C=CC(O)=O)=C(C(=O)OC)NC2=C1 XYFRHHAYSXIKGH-UHFFFAOYSA-N 0.000 description 1
MKTOIPPVFPJEQO-UHFFFAOYSA-N 4-(3-carboxypropanoylperoxy)-4-oxobutanoic acid Chemical compound OC(=O)CCC(=O)OOC(=O)CCC(O)=O MKTOIPPVFPJEQO-UHFFFAOYSA-N 0.000 description 1
239000004342 Benzoyl peroxide Substances 0.000 description 1
OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 1
101100494448 Caenorhabditis elegans cab-1 gene Proteins 0.000 description 1
YIVJZNGAASQVEM-UHFFFAOYSA-N Lauroyl peroxide Chemical compound CCCCCCCCCCCC(=O)OOC(=O)CCCCCCCCCCC YIVJZNGAASQVEM-UHFFFAOYSA-N 0.000 description 1
244000028419 Styrax benzoin Species 0.000 description 1
235000000126 Styrax benzoin Nutrition 0.000 description 1
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
235000008411 Sumatra benzointree Nutrition 0.000 description 1
JUIBLDFFVYKUAC-UHFFFAOYSA-N [5-(2-ethylhexanoylperoxy)-2,5-dimethylhexan-2-yl] 2-ethylhexaneperoxoate Chemical compound CCCCC(CC)C(=O)OOC(C)(C)CCC(C)(C)OOC(=O)C(CC)CCCC JUIBLDFFVYKUAC-UHFFFAOYSA-N 0.000 description 1
230000000996 additive effect Effects 0.000 description 1
150000001336 alkenes Chemical class 0.000 description 1
125000000751 azo group Chemical group [*]N=N[*] 0.000 description 1
229960002130 benzoin Drugs 0.000 description 1
235000019400 benzoyl peroxide Nutrition 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
238000005266 casting Methods 0.000 description 1
229920001577 copolymer Polymers 0.000 description 1
150000001925 cycloalkenes Chemical class 0.000 description 1
URYYVOIYTNXXBN-UPHRSURJSA-N cyclooctene Chemical compound C1CCC\C=C/CC1 URYYVOIYTNXXBN-UPHRSURJSA-N 0.000 description 1
239000004913 cyclooctene Substances 0.000 description 1
XJOBOFWTZOKMOH-UHFFFAOYSA-N decanoyl decaneperoxoate Chemical compound CCCCCCCCCC(=O)OOC(=O)CCCCCCCCC XJOBOFWTZOKMOH-UHFFFAOYSA-N 0.000 description 1
ISAOCJYIOMOJEB-UHFFFAOYSA-N desyl alcohol Natural products C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 description 1
125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
230000000694 effects Effects 0.000 description 1
238000010894 electron beam technology Methods 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
230000002349 favourable effect Effects 0.000 description 1
239000011521 glass Substances 0.000 description 1
235000019382 gum benzoic Nutrition 0.000 description 1
150000008282 halocarbons Chemical class 0.000 description 1
125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 1
125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
239000012442 inert solvent Substances 0.000 description 1
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
238000005259 measurement Methods 0.000 description 1
230000007246 mechanism Effects 0.000 description 1
239000000178 monomer Substances 0.000 description 1
FEZFGASTIQVZSC-UHFFFAOYSA-N nonanoyl nonaneperoxoate Chemical compound CCCCCCCCC(=O)OOC(=O)CCCCCCCC FEZFGASTIQVZSC-UHFFFAOYSA-N 0.000 description 1
125000004430 oxygen atom Chemical group O* 0.000 description 1
125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
150000002978 peroxides Chemical class 0.000 description 1
125000000864 peroxy group Chemical group O(O*)* 0.000 description 1
BWJUFXUULUEGMA-UHFFFAOYSA-N propan-2-yl propan-2-yloxycarbonyloxy carbonate Chemical compound CC(C)OC(=O)OOC(=O)OC(C)C BWJUFXUULUEGMA-UHFFFAOYSA-N 0.000 description 1
KOPQZJAYZFAPBC-UHFFFAOYSA-N propanoyl propaneperoxoate Chemical compound CCC(=O)OOC(=O)CC KOPQZJAYZFAPBC-UHFFFAOYSA-N 0.000 description 1
239000002904 solvent Substances 0.000 description 1
150000003440 styrenes Chemical class 0.000 description 1
229910052717 sulfur Inorganic materials 0.000 description 1
239000011593 sulfur Substances 0.000 description 1
QHDZGOLELSOUFO-UHFFFAOYSA-N tert-butyl butaneperoxoate Chemical compound CCCC(=O)OOC(C)(C)C QHDZGOLELSOUFO-UHFFFAOYSA-N 0.000 description 1
BWSZXUOMATYHHI-UHFFFAOYSA-N tert-butyl octaneperoxoate Chemical compound CCCCCCCC(=O)OOC(C)(C)C BWSZXUOMATYHHI-UHFFFAOYSA-N 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
238000003856 thermoforming Methods 0.000 description 1
239000012815 thermoplastic material Substances 0.000 description 1
230000001960 triggered effect Effects 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1

Classifications

- G—PHYSICS
- G02—OPTICS
- G02C—SPECTACLES; SUNGLASSES OR GOGGLES INSOFAR AS THEY HAVE THE SAME FEATURES AS SPECTACLES; CONTACT LENSES
- G02C7/00—Optical parts
- G02C7/02—Lenses; Lens systems ; Methods of designing lenses
- G02C7/04—Contact lenses for the eyes
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B1/00—Optical elements characterised by the material of which they are made; Optical coatings for optical elements
- G02B1/04—Optical elements characterised by the material of which they are made; Optical coatings for optical elements made of organic materials, e.g. plastics
- G02B1/041—Lenses
- G02B1/043—Contact lenses

Landscapes

Physics & Mathematics (AREA)
General Physics & Mathematics (AREA)
Optics & Photonics (AREA)
Health & Medical Sciences (AREA)
Ophthalmology & Optometry (AREA)
General Health & Medical Sciences (AREA)
Eyeglasses (AREA)
Silicon Polymers (AREA)
Casting Or Compression Moulding Of Plastics Or The Like (AREA)
Macromonomer-Based Addition Polymer (AREA)

IL10103592A 1991-02-28 1992-02-21 Contact lenses made of thermally designed material IL101035A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CH60491		1991-02-28

Publications (2)

Publication Number	Publication Date
IL101035A0 IL101035A0 (en)	1992-11-15
IL101035A true IL101035A (en)	1995-06-29

Family

ID=4190838

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
IL10103592A IL101035A (en)	1991-02-28	1992-02-21	Contact lenses made of thermally designed material

Country Status (11)

Country	Link
US (1)	US5198477A (fr)
EP (1)	EP0501917A3 (fr)
JP (1)	JPH05127134A (fr)
KR (1)	KR920016871A (fr)
AU (1)	AU647880B2 (fr)
CA (1)	CA2061923A1 (fr)
CS (1)	CS58192A3 (fr)
HU (1)	HUT63502A (fr)
IE (1)	IE920632A1 (fr)
IL (1)	IL101035A (fr)
ZA (1)	ZA921454B (fr)

Families Citing this family (28)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
AU2966595A (en) *	1994-07-26	1996-02-22	Bausch & Lomb Incorporated	Method of polymerizing methacrylate-based compositions
US6367929B1 (en)	1998-03-02	2002-04-09	Johnson & Johnson Vision Care, Inc.	Hydrogel with internal wetting agent
US7473738B2 (en) *	2004-09-30	2009-01-06	Johnson & Johnson Vision Care, Inc.	Lactam polymer derivatives
DE102005036520A1 (de) *	2005-04-26	2006-11-09	Osram Opto Semiconductors Gmbh	Optisches Bauteil, optoelektronisches Bauelement mit dem Bauteil und dessen Herstellung
US7858000B2 (en) *	2006-06-08	2010-12-28	Novartis Ag	Method of making silicone hydrogel contact lenses
ES2346812T3 (es)	2006-07-12	2010-10-20	Novartis Ag	Copolimeros actinicamente entrelazables para la fabricacion de lentes de contacto.
AR064286A1 (es) *	2006-12-13	2009-03-25	Quiceno Gomez Alexandra Lorena	Produccion de dispositivos oftalmicos basados en la polimerizacion por crecimiento escalonado fotoinducida
MX2009010109A (es)	2007-03-22	2009-10-12	Novartis Ag	Prepolimeros que contienen silicona con cadenas polimericas hidrofilicas.
EP2129513B1 (fr)	2007-03-22	2016-08-03	Novartis AG	Prépolymères avec chaînes polymères contenant du poly(siloxane) pendillant
TWI551305B (zh) *	2007-08-31	2016-10-01	諾華公司	相對黏稠封裝溶液之用途
KR101535692B1 (ko)	2007-08-31	2015-07-09	노파르티스 아게	콘택트 렌즈 포장 용액
CA2730506A1 (fr)	2008-07-21	2010-01-28	Novartis Ag	Materiaux polymeres contenant de la silicone a groupes pouvant etre hydrolyses
CA2731159A1 (fr)	2008-07-21	2010-01-28	Novartis Ag	Lentilles de contact en hydrogel de silicone a agents de confort convertibles
AR074110A1 (es) *	2008-11-13	2010-12-22	Novartis Ag	Copolimeros de polisiloxano con cadenas de polimero hidrofilicas terminales
TWI506333B (zh)	2008-12-05	2015-11-01	Novartis Ag	用以傳遞疏水性舒適劑之眼用裝置及其製造方法
JP5947723B2 (ja) *	2009-11-17	2016-07-06	ノバルティスアーゲー	コンタクトレンズの消毒のための過酸化水素溶液及びキット
TWI399399B (zh)	2010-03-30	2013-06-21	Taiwan Textile Res Inst	網狀結構纖維素母粒之製備方法與應用
TWI522395B (zh)	2010-07-30	2016-02-21	諾華公司	兩親性聚矽氧烷預聚物及其用途
EP2625216B1 (fr)	2010-10-06	2019-06-05	Novartis AG	Polysiloxanes polymerisables a chaine allongee avec des groupes hydrophiles pendants
WO2012047964A1 (fr)	2010-10-06	2012-04-12	Novartis Ag	Agents de réticulation de polysiloxane à chaîne étendue avec des chaînes de polymère hydrophile pendantes
NZ606787A (en)	2010-10-06	2014-11-28	Novartis Ag	Water-processable silicone-containing prepolymers and uses thereof
WO2012170603A1 (fr)	2011-06-09	2012-12-13	Novartis Ag	Lentilles en silicone hydrogel pourvues de surfaces nanotexturées
JP5452756B1 (ja)	2013-07-02	2014-03-26	Ｈｏｙａ株式会社	親水性表面を有するシリコーン含有共重合体成形品を作製する方法及び親水性表面を有するシリコーンハイドロゲルコンタクトレンズ
MY186090A (en)	2015-12-03	2021-06-21	Alcon Inc	Contact lens packaging solutions
US12072556B2 (en)	2019-11-04	2024-08-27	Alcon Inc.	Contact lenses with surfaces having different softness
TWI859401B (zh)	2020-01-27	2024-10-21	新加坡商科萊博新加坡私人有限公司	光化可交聯的聚矽氧烷－聚甘油嵌段共聚物及其製造和使用方法
US12358247B2 (en)	2020-07-28	2025-07-15	Alcon Inc.	Contact lenses with softer lens surfaces
JP2025525733A (ja)	2022-08-17	2025-08-07	アルコンインク．	ハイドロゲルコーティングをその上に有するコンタクトレンズ

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3445093A1 (de) *	1984-12-11	1986-06-19	Bayer Ag, 5090 Leverkusen	Hydrophile copolymere, deren verwendung als biomedizinische materialien und hieraus hergestellte kontaktoptische gegenstaende
JPH0830106B2 (ja) *	1989-06-24	1996-03-27	日本ゼオン株式会社	成形用材料

1992
- 1992-02-07 AU AU10835/92A patent/AU647880B2/en not_active Ceased
- 1992-02-19 EP EP19920810120 patent/EP0501917A3/de not_active Ceased
- 1992-02-21 IL IL10103592A patent/IL101035A/en not_active IP Right Cessation
- 1992-02-25 US US07/841,920 patent/US5198477A/en not_active Expired - Fee Related
- 1992-02-26 CA CA002061923A patent/CA2061923A1/fr not_active Abandoned
- 1992-02-26 KR KR1019920002960A patent/KR920016871A/ko not_active Withdrawn
- 1992-02-27 IE IE063292A patent/IE920632A1/en not_active Application Discontinuation
- 1992-02-27 HU HU9200657A patent/HUT63502A/hu unknown
- 1992-02-27 CS CS92581A patent/CS58192A3/cs unknown
- 1992-02-27 ZA ZA921454A patent/ZA921454B/xx unknown
- 1992-02-28 JP JP4075972A patent/JPH05127134A/ja active Pending

Also Published As

Publication number	Publication date
JPH05127134A (ja)	1993-05-25
KR920016871A (ko)	1992-09-25
EP0501917A3 (en)	1993-02-03
IE920632A1 (en)	1992-09-09
IL101035A0 (en)	1992-11-15
CS58192A3 (en)	1992-09-16
AU1083592A (en)	1992-09-03
AU647880B2 (en)	1994-03-31
HUT63502A (en)	1993-08-30
CA2061923A1 (fr)	1992-08-29
EP0501917A2 (fr)	1992-09-02
HU9200657D0 (en)	1992-05-28
US5198477A (en)	1993-03-30
ZA921454B (en)	1992-10-28

Legal Events

Date	Code	Title	Description
1999-01-26	RH	Patent void

Publication	Publication Date	Title
US5198477A (en)	1993-03-30	Contact lenses made from thermoformable material
US4343927A (en)	1982-08-10	Hydrophilic, soft and oxygen permeable copolymer compositions
CA2152258C (fr)	2000-05-16	Nouveaux macromonomeres
US4182822A (en)	1980-01-08	Hydrophilic, soft and oxygen permeable copolymer composition
US5244981A (en)	1993-09-14	Silicone-containing contact lens polymers, oxygen permeable contact lenses and methods for making these lenses and treating patients with visual impairment
US5057578A (en)	1991-10-15	Silicone-containing block copolymers and macromonomers
US4954587A (en)	1990-09-04	Dimethylacrylamide-copolymer hydrogels with high oxygen permeability
US4743667A (en)	1988-05-10	Contact lens material
JP3487930B2 (ja)	2004-01-19	架橋させ得る共重合体およびヒドロゲル
CA2027748C (fr)	1998-01-06	Compositions polymeriques pour les lentilles de contact permeables a l'oxygene
JP3441024B2 (ja)	2003-08-25	親水性含フッ素シロキサンモノマー及びその樹脂からなる眼科用レンズ材料
EP2255228A1 (fr)	2010-12-01	Lentilles comprenant des copolymères multiséquencés amphiphiles
CA1338363C (fr)	1996-05-28	Hydrogels formes de copolymeres de dimethylacrylamide, ayant une grande permeabilite a l'oxygene
IL97978A (en)	1994-12-29	Polymers and hard gas-permeable contact lenses made of them
US4788227A (en)	1988-11-29	Contact lens formed from a hydrogel fundamental material
JPH0529091B2 (fr)	1993-04-28
AU662170B2 (en)	1995-08-24	Copolymers comprising propellanes and contact lenses made therefrom
SU1085986A1 (ru)	1984-04-15	Способ получени привитых сополимеров
EP0947857A2 (fr)	1999-10-06	Procédé de fabrication d' un article optique et un article optique obtenu par ce procédé
JPS61141717A (ja)	1986-06-28	ヒドロゲル基材
HK1001590B (en)	1998-06-26	Novel macromonomers