IP Library Granted Patent US 8,987,403
Granted Patent B2
US 8,987,403 · App. 14/014,631 · Granted Mar 24, 2015

Amphiphilic polysiloxane prepolymers and uses thereof

View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 8,987,403
App. No.
14/014,631
Granted
Mar 24, 2015
Kind
B2
Abstract

The present invention provides an amphiphilic polysiloxane prepolymer which comprises hydrophilic monomeric units derived from at least one hydrophilic vinylic monomer, polysiloxane crosslinking units derived from at least one polysiloxane crosslinker having at least two terminal ethylenically-unsaturated groups, dangling polysiloxane chains each of which is terminated with one ethylenically unsaturated group, and chain-transfer units derived from a chain transfer agent other than a RAFT agent. A prepolymer of the invention is suitable for making hydrogel contact lenses. The present invention is also related to hydrogel contact lenses made from an amphiphilic polysiloxane prepolymer of the invention and to processes for preparing an amphiphilic polysiloxane prepolymer of the invention and for making silicone hydrogel contact lenses.

Claims (17)

1. A partially ethylenically-functionalized polysiloxane, which is a mixture of reaction products obtained by reacting an ethylenically functionalizing vinylic monomer having a first reactive functional group with a linear functional polysiloxane compound having two terminal second reactive functional groups at a molar equivalent ratio, R Equivalent , of from about 40% to about 97%, wherein each first reactive functional group reacts with one second reactive functional group in the presence or absence of a coupling agent to form a covalent bond or linkage, wherein the mixture of reaction product comprises (R Equivalent ) 2 ×100% by mole of a linear polysiloxane crosslinkers having two terminal ethylenically-unsaturated groups, 2×R Equivalent ×(1−R Equivalent )×100% by mole of a polysiloxane vinylic monomer or macromer having one terminal second reactive functional group and one terminal ethylenically-unsaturated group, and (1−R Equivalent )×(1−R Equivalent )×100% by mole of unreacted linear polysiloxane compound with two terminal second reactive functional groups.

2. The partially ethylenically-functionalized polysiloxane of claim 1 , wherein R Equivalent is from about 50% to about 95%.

3. The partially ethylenically-functionalized polysiloxane of claim 1 , wherein R Equivalent is from about 60% to about 92%.

4. The partially ethylenically-functionalized polysiloxane of claim 1 , wherein R Equivalent is from about 70% to about 90%.

5. The partially ethylenically-functionalized polysiloxane of claim 1 , wherein the linear functional polysiloxane compound is defined by formula (1)

FG-G 1 -PDMS-G 2 -FG  (1)

CR(-G 1 -PDMS-G 2 -FG) a1   (2)

in which

G 1 and G 2 independent of each other are a linear or branched C 1 -C 10 alkylene divalent radical, a divalent radical of alk′-O q alk- in which q is an integer of from 1 to 5 and alk and alk′ independent of each other is a C 1 -C 6 alkylene divalent radical, or a divalent radical of -R′ 1 -X 1 -E-X 2 -R′ 2 -in which R′ 1 and R′ 2 independent of each other is a linear or branched C 1 -C 10 alkylene divalent radical or a divalent radical of alk′-O q alk- as defined above, X 1 and X 2 independent of each other are a linkage selected from the group consisting of

 in which R′ is H or C 1 -C 8 alkyl, E is an alkyl diradical, a cycloalkyl diradical, an alkylcycloalkyl diradical, an alkylaryl diradical, or an aryl diradical with up to 40 carbon atoms which may have ether, thio, or amine linkages in the main chain;

PDMS is a polysiloxane divalent radical of formula (3)

in which ν is 0 or 1, ω is an integer of from 0 to 5, U 1 and U 2 independent of each other represent a divalent radical of -R′ 1 -X 1 -E-X 2 -R′ 2 - as defined above or a divalent radical of alk′-O q alk- as defined above, D 1 , D 2 and D 3 independently of each other are a divalent radical selected from the group consisting of —(CH 2 CH 2 O) t —CH 2 CH 2 — in which t is an integer of 3 to 40, —CF 2 —(OCF 2 ) a —(OCF 2 CF 2 ) b —OCF 2 — in which a and b independent of each other is an integer of 0 to 10 provided that a+b is a number in the range of 10 to 30, and a divalent group of formula (4)

in which R 3 , R 4 , R 5 ′, R 6 , R 7 , R 8 , R 9 and R 10 , independently of one another, are C 1 -C 10 alkyl, C 1 -C 10 aminoalkyl, C 1 -C 10 hydroxyalkyl, C 1 -C 10 ether, C 1 -C 4 alkyl- or C 1 -C 4 -alkoxy-substituted phenyl, C 1 -C 10 fluoroalkyl, C 1 -C 10 fluoroether, C 6 -C 18 aryl radical, cyano(C 1 -C 12 -alkyl), -alk-(OCH 2 CH 2 ) n —OR 11 , in which alk is C 1 -C 6 alkylene divalent radical, R 11 is hydrogen or C 1 -C 6 alkyl, and n is an integer of from 1 to 10; m and p independently of each other are an integer of from 0 to 350 and (m+p) is from 1 to 700, provided that at least one of D 1 , D 2 and D 3 is represented by formula (4);

CR is a multivalent organic radical having a valence of a1;

a1 is an integer of 3, 4 or 5; and

FG is selected from the group consisting of amino group (—NHR′ as defined above), hydroxyl group, carboxylic acid group, acid halide groups (—COX, X═Cl, Br, or I), acid anhydrate group, aldehyde group, azlactone group, isocyanate group, epoxy group, aziridine group, thiol (—SH), and amide groups (—CONH 2 ).

6. The partially ethylenically-functionalized polysiloxane of claim 5 , wherein the ethylenically functionalizing vinylic monomer is selected from the group consisting of C 1 to C 6 hydroxylalkyl (meth)acrylate, C 1 to C 6 hydroxyalkyl (meth)acrylamide, C 1 to C 6 aminoalkyl (meth)acrylate, allylalcohol, allylamine, C 1 to C 6 aminoalkyl (meth)acrylamide, aziridinyl C 1 -C 12 alkyl (meth)acrylate (e.g., 2-(1-aziridinyl) ethyl (meth)acrylate, 3-(1-aziridinyl) propyl (meth)acrylate, 4-(1-aziridinyl) butyl (meth)acrylate, 6-(1-aziridinyl) hexyl (meth)acrylate, or 8-(1-axiridinyl) octyl (meth)acrylate), glycidyl (meth)acrylate, C 1 to C 6 alkyl (meth)acrylic acid, (meth)acrylic acid halide (—COX, X═Cl, Br, or I), C 1 to C 6 isocyanatoalkyl (meth)acrylate, 2-vinyl-4,4-dimethyl-1,3-oxazolin-5-one, 2-isopropenyl-4,4-dimethyl-1,3-oxazolin-5-one, 2-vinyl-4-methyl-4-ethyl-1,3-oxazolin-5-one, 2-isopropenyl-4-methyl-4-butyl-1,3-oxazolin-5-one, 2-vinyl-4,4-dibutyl-1,3-oxazolin-5-one, 2-isopropenyl-4-methyl-4-dodecyl-1,3-oxazolin-5-one, 2-isopropenyl-4,4-diphenyl-1,3-oxazolin-5-one, 2-isopropenyl-4,4-pentamethylene-1,3-oxazolin-5-one, 2-isopropenyl-4,4-tetramethylene-1,3-oxazolin-5-one, 2-vinyl-4,4-diethyl-1,3-oxazolin-5-one, 2-vinyl-4-methyl-4-nonyl-1,3-oxazolin-5-one, 2-isopropenyl-4-methyl-4-phenyl-1,3-oxazolin-5-one, 2-isopropenyl-4-methyl-4-benzyl-1,3-oxazolin-5-one, 2-vinyl-4,4-pentamethylene-1,3-oxazolin-5-one, and 2-vinyl-4,4-dimethyl-1,3-oxazolin-6-one, with 2-vinyl-4,4-dimethyl-1,3-oxazolin-5-one (VDMO), 2-isopropenyl-4,4-dimethyl-1,3-oxazolin-5-one (IPDMO), and combinations thereof.

Assignments (3)
CONFIRMATORY DEED OF ASSIGNMENT EFFECTIVE APRIL 8, 2019 Recorded Dec 10, 2019
From: NOVARTIS AG
To: ALCON INC.
Reel/Frame 051454/0788 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 9, 2015
From: CHANG, FRANK; SCOTT, ROBERT; HUANG, JINYU; MEDINA, ARTURO N.; SMITH, DAWN A.; SANDERS, LAURA ANN; PRUITT, JOHN DALLAS
To: NOVARTIS AG
Reel/Frame 034915/0626 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 15, 2014
From: CHANG, FRANK; SCOTT, ROBERT; HUANG, JINYU; MEDINA, ARTURO N; SMITH, DAWN A.; SANDERS, LAURA ANN; PRUITT, JOHN DALLAS
To: NOVARTIS AG
Reel/Frame 032674/0339 →