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US4440919A Expired / Lapsed US ⏱️ 0.0 years remaining

Low N-vinyl lactam content based biomedical devices

Assignee: Bausch and Lomb Inc
•
Filing: 1981-11-12
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Granted: 1984-04-03
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Expires: 2001-11-12
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Abstract

Abstract Low N-vinyl lactam content copolymers are cross-linked with resonance free di(alkene tertiary amine) cyclic compounds to obtain biomedical devices, including soft contact lenses, which have good oxygen permeability and mechanical properties.

Inventors

  • 👤 Richard C. Chromecek
  • 👤 Gary D. Friends
  • 👤 Lawrence Y. Wissman
  • 👤 Raymond A. Yourd, III

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-23 20:16
CPC Classifications
G; G02; G02B; G02B1/00; G02B1/04; G02B1/041; G02B1/043; A; A61; A61L; A61L27/00; A61L27/14; A61L27/16; A61L33/00; A61L33/06; A61L33/064; B; B01; B01D; B01D71/00; B01D71/06; B01D71/44; B01D71/441; C; C08; C08F; C08F226/00; C08F226/06

Claims Analysis

Total Claims: 22
Claim 1
Independent Claim 230 words
As a new article of manufacture a contact lens formed from a hydrophilic polymer formed by polymerizing (a) one or more N-vinyl lactams and/or heterocyclic N-vinyl monomers, said N-vinyl lactams being selected from the group consisting of N-vinyl-2-pyrrolidinone, N-(1-methyl) vinyl pyrrolidinone, N-vinyl-2-piperidone and N-vinyl-2-caprolactam which may be substituted in the lactam ring by one or more lower alkyl groups, said heterocyclic N-vinyl monomers being selected from the group consisting of N-vinyl imidazole, N-vinyl succinimide, N-vinyl diglycolylimide, N-vinyl glutarimide, N-vinyl-3-morpholinone and N-vinyl-5-methyl-3-morpholinone, (b) one or more hydrophilic comonomers selected from the group consisting of hydroxyesters, free acids, amides and amines of acrylates, methacrylates, or itaconates, said hydrophilic monomer(s) being at least 50% of the total monomer of (a) and (b) present and (c) a resonance free di(alkene tertiary amine) cyclic crosslinking agent, said cyclic compound having the formula CH 2 :CG(CH 2 ) x N˜J˜N (CH 2 ) x CG:CH 2 wherein x is 0 or 1, G is hydrogen or methyl and J is the balance of a structure forming cyclic dialkene urea, said agent being present in an amount from 0.01 to 10 weight percent of the total monomers of (a) and (b) present to form a crosslinked 3-dimensional polymeric network, said polymer having an oxygen permeability of at least 8×10 -11 cm 2 cm/sec.cm 2 mmHg) and a tear initiation strength of at least 2 g/mm of thickness.
Claim 2
Dependent Claim 230 words
As a new article of manufacture a contact lens formed from a hydrophilic polymer formed by polymerizing (a) one or more N-vinyl lactams and/or heterocyclic N-vinyl monomers, said N-vinyl lactams being selected from the group consisting of N-vinyl-2-pyrrolidinone, N-(1-methyl) vinyl pyrrolidinone, N-vinyl-2-piperidone and N-vinyl-2-caprolactam which may be substituted in the lactam ring by one or more lower alkyl groups, said heterocyclic N-vinyl monomers being selected from the group consisting of N-vinyl imidazole, N-vinyl succinimide, N-vinyl diglycolylimide, N-vinyl glutarimide, N-vinyl-3-morpholinone and N-vinyl-5-methyl-3-morpholinone, (b) one or more hydrophilic comonomers selected from the group consisting of hydroxyesters, free acids, amides and amines of acrylates, methacrylates, or itaconates, said hydrophilic monomer(s) being at least 50% of the total monomer of (a) and (b) present and (c) a resonance free di(alkene tertiary amine) cyclic crosslinking agent, said cyclic compound having the formula CH 2 :CG(CH 2 ) x N˜J˜N (CH 2 ) x CG:CH 2 wherein x is 0 or 1, G is hydrogen or methyl and J is the balance of a structure forming cyclic dialkene urea, said agent being present in an amount from 0.01 to 10 weight percent of the total monomers of (a) and (b) present to form a crosslinked 3-dimensional polymeric network, said polymer having an oxygen permeability of at least 8×10 -11 cm 2 cm/sec.cm 2 mmHg) and a tear initiation strength of at least 2 g/mm of thickness.
Claim 3
Dependent Claim 51 words
The article according to claim 1 wherein the resonance free di(alkene tertiary amine) cyclic compound is selected from the group consisting of cyclic dialkene urea, dialkene amides, dialkene hydrazides, dialkene hydantoins, dialkene hydrouracils, dialkene 2,2'-bis-imidazolin and mixtures thereof, said alkene being either vinyl, alpha methyl vinyl, alpha methyl allyl or allyl.
Claim 4
Dependent Claim 20 words
The article according to claim 1 wherein the resonance free di(alkene tertiary amine) cyclic compound is a cyclic divinyl urea.
Claim 5
Dependent Claim 15 words
The article according to claim 3 wherein the cyclic divinyl urea is divinyl ethylene urea.
Claim 6
Dependent Claim 14 words
The article according to claim 2 wherein the cyclic compound is a dialkene 2,2'-bis-imidazolin.
Claim 7
Dependent Claim 12 words
The article according to claim 5 wherein the dialkene 2,2'-bis-imidazolin is 1,1'-divinyl-2,2'-bis-imidazolin.
Claim 8
Dependent Claim 11 words
The article according to claim 5 wherein the 2,2'-bis-imidazolin is 1,1'-diallyl-2,2'-bis-imidazolin.
Claim 9
Dependent Claim 20 words
The article according to claim 2 wherein the resonance free di(alkene tertiary amine) cyclic compound is a cyclic allyl urea.
Claim 10
Dependent Claim 15 words
The article according to claim 8 wherein the cyclic allyl urea is diallyl ethylene urea.
Claim 11
Dependent Claim 21 words
The article according to claim 1 wherein the crosslinking agent is present in an amount from 0.1 to 3.0 weight percent.
Claim 12
Dependent Claim 18 words
The article according to claim 1 wherein the N-vinyl lactam and/or heterocyclic N-vinyl monomer is an N-vinyl lactam.
Claim 13
Dependent Claim 12 words
The article according to claim 11 wherein the N-vinyl lactam is N-vinyl-2-pyrrolidinone.
Claim 14
Dependent Claim 12 words
The article according to claim 11 wherein the N-vinyl lactam is N-vinyl-2-caprolactam.
Claim 15
Dependent Claim 19 words
The article according to claim 1 wherein the N-vinyl lactam and/or heterocyclic N-vinyl monomer is a heterocyclic N-vinyl monomer.
Claim 16
Dependent Claim 13 words
The article according to claim 14 wherein the heterocyclic N-vinyl monomer is N-vinyl-5-methyl-3-morpholinone.
Claim 17
Dependent Claim 14 words
The article according to claim 14 wherein the heterocyclic N-vinyl monomer is N-vinyl glutarimide.
Claim 18
Dependent Claim 47 words
The article according to claim 1 wherein from 15% to 40% by weight of the total monomers employed is the N-vinyl lactam or a mixture of the N-vinyl lactams and from 60% to 85% by weight is the hydrophilic comonomer or a mixture of the hydrophilic comonomers.
Claim 19
Dependent Claim 20 words
The article according to claim 17 wherein the N-vinyl lactam is N-vinyl pyrrolidinone and the hydrophilic comonomer is hydroxyethyl methacrylate.
Claim 20
Dependent Claim 20 words
The article according to claim 17 wherein the N-vinyl lactam is N-vinyl pyrrolidinone and the hydrophilic comonomer is hydroxypropyl methacrylate.
Claim 21
Dependent Claim 51 words
A process for preparing the article of claim 1 comprising (a) admixing together the monomers and crosslinking agent with a free radical initiator, (b) charging the mixture to a mold and (c) activating and maintaining the activation of the free radical initiator until the desired degree of crosslinking has been obtained.
Claim 22
Dependent Claim 37 words
The process of claim 20 wherein a water soluble or solvent soluble diluent is admixed with the monomer and crosslinking agent and after the article has been formed removing the diluent by washing the article with water.

References Cited (Backward Citations)

US2541152A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1987-04-03 1987-10-03 1988-04-03 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1991-04-03 1991-10-03 1992-04-03 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1995-04-03 1995-10-03 1996-04-03 $7700.00 Window Closed / Lapsed

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