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US4414375A Expired / Lapsed US ⏱️ 0.0 years remaining

Oxygen permeable contact lens material comprising copolymers of multifunctional siloxanyl alkylesters

Assignee: DOME PATENT LP A CA PARTNERSHIP
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Filing: 1981-09-08
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Granted: 1983-11-08
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Expires: 2001-09-08
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Abstract

Abstract An oxygen permeable contact lens fabricated from a copolymer of a multifunctional siloxanyl alkylester a monomer selected from the group consisting of, an ester of acrylic or methacrylic acid and from an ester of itaconic acid or mixture thereof. The copolymer can be made either hard, soft, or elasticmeric with improved oxygen permeability.

Inventors

  • 👤 Russell A. Neefe

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-27 08:55
CPC Classifications
C; C08; C08F; C08F30/00; C08F30/04; C08F30/08; G; G02; G02B; G02B1/00; G02B1/04

Claims Analysis

Total Claims: 7
Claim 1
Independent Claim 124 words
An oxygen permeable material for the manufacture of contact lenses formed by copolymerizing (a) from 5 to 90% by weight of a multifunctional siloxanyl alkyl ester, monomer having two or more α, ω terminally bonded through divalent hydrocarbon groups to an activated unsaturated group, (b) an effective amount of a copolymerizable monomer up to 90% by weight of an ester of acrylic or methacrylic acid or mixture thereof, or from (c) an effective amount of a copolymerizable monomer up an ester of itaconic acid, (d) from 0.5 to 40% by weight of a hydrophilic monomer for a surface wetting agent, and (e) from 0 to 20% by weight of an ester crosslinking agent in the presence of a free radical or a photo initiator.
Claim 2
Dependent Claim 124 words
An oxygen permeable material for the manufacture of contact lenses formed by copolymerizing (a) from 5 to 90% by weight of a multifunctional siloxanyl alkyl ester, monomer having two or more α, ω terminally bonded through divalent hydrocarbon groups to an activated unsaturated group, (b) an effective amount of a copolymerizable monomer up to 90% by weight of an ester of acrylic or methacrylic acid or mixture thereof, or from (c) an effective amount of a copolymerizable monomer up an ester of itaconic acid, (d) from 0.5 to 40% by weight of a hydrophilic monomer for a surface wetting agent, and (e) from 0 to 20% by weight of an ester crosslinking agent in the presence of a free radical or a photo initiator.
Claim 3
Dependent Claim 47 words
A composition as defined in claim 1 wherein said multifunctional siloxanyl alkyl ester monomer having two or more α, ω terminally bonded through divalent hydrocarbon groups to an activated unsaturated groups; includes at least one of the following group: tetrakis-(trimethylsiloxy)bis(methacryloxypropyl)disiloxane tetrakis-(trimethylsiloxy)bis(methacryloxypropyl)dimethyltrisiloxane pentakis-(trimethylsiloxy)tris(methacryoxypropyl)tetramethyl-pentasiloxane hexakis-(trimethylsiloxy)tetrakis-(methacryloxpropyl)-hexamethyl heptasiloxane tris-(methacryloxymethyldimethylsiloxy)methacryloxypropylsiloxane tetrakis-(methacryloxymethyldimethylsiloxy)tetramethylcyclotetra-siloxane tetrakis-(methacryloxymethyldimethylsiloxy)siloxane.
Claim 4
Dependent Claim 53 words
A composition as defined in claim 1 wherein said ester of acrylic or methacrylic acid include at least one of the following group: butyl acrylate, butyl methacrylate cyclohexyl acrylate, cyclohexyl methacrylate 2-ethylacrylate, 2-ethylmethacrylate glycidyl acrylate, glycidyl methacrylate hexyl acrylate, hexyl methacrylate lauryl acrylate, lauryl methacrylate methyl acrylate, methyl methacrylate stearyl acrylate, stearyl methacrylate.
Claim 5
Dependent Claim 33 words
A composition as defined in claim 1 wherein said ester of itaconic acid include at least one of the following group: butyl itaconate dibutyl itaconate methyl itaconate dimethyl itaconate phenyl itaconate diphenyl itaconate.
Claim 6
Dependent Claim 76 words
A composition as defined in claim 1 wherein said a hydrophiliomonomer for a surface wetting agent include at least one of the following group: acrylamide 2-acrylamido-2 methyl propane sulfonic acid t-butylaminoethyl methacrylate dimethylaminoethylacrylate, dimethylaminoethylmethacrylate N-(1,1-dimethyl-3-oxobutyl)acrylamide glacial acrylic acid, glacial methacrylic acid glyceryl acrylate, glyceryl methacrylate itaconic acid propylene glycolmonoacrylate, propylene glycol monomethacrylate ethylene glycol monoacrylate, ethylene glycol monomethacrylate methacrylamide morpholinoethyl acrylate, morphilinoethyl methacrylate piperidinoethyl acrylate, piperidinoethyl methacrylate triethylene glycol methacrylate N-vinyl pyrrolidone dihydroxypropyl acrylate, dihydroxypropyl methacrylate.
Claim 7
Dependent Claim 55 words
A composition as defined in claim 1 wherein said an ester crosslinking agent include at least one of the following group: bis(methacryloxypropyl)tetramethyldisiloxane 1,3 bis(glycidoxypropyl)tetramethyldisiloxane divinyl diphenyl silane ethylene glycol diacrylate, ethylene glycol dimethacrylate diethylene glycol dicacrylate, diethylene glycol dimethacrylate trimethylpropane triacrylate, trimethylpropane trimethacrylate triethylene glycol diacrylate, triethylene glycol dimethacrylate tetraethylene glycol diacrylate, tetraethylene glycol dimethacrylate.

References Cited (Backward Citations)

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USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1986-11-07 1987-05-09 1987-11-08 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1990-11-07 1991-05-09 1991-11-08 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1994-11-07 1995-05-09 1995-11-08 $7700.00 Window Closed / Lapsed

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