IP Library Granted Patent US 8,318,059
Granted Patent B2
US 8,318,059 · App. 12/456,409 · Granted Nov 27, 2012

Stabilization of poly(oxyalkylene) containing polymeric materials

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Quick Facts
Patent No.
US 8,318,059
App. No.
12/456,409
Granted
Nov 27, 2012
Kind
B2
Abstract

The present invention provides a method for producing a medical device, preferably an ophthalmic device, more preferably a contact lens, made of a stabilized poly(oxyalkylene)-containing polymeric material. The method of the invention comprises the steps of: curing, in a mold, a composition comprising (a) a prepolymer having at least one poly(oxyalkylene) unit, (b) a biocompatible organic multi-acid or biocompatible salt thereof in an amount sufficient to improve the stability of the poly(oxyalkylene)-containing polymer made from the composition, (c) optionally a photoinitiator or a thermal initiator, and (d) optionally one or more vinylic monomers, to form the medical device being less susceptible to oxidative degradation; and removing the medical device from the mold.

Claims (4)

1. A method for sterilizing a medical device having a core material and/or a coating, wherein the core material and the coating, independently of each other, are made of a poly(oxyalkylene)-containing polymeric material, the method comprising: autoclaving the medical device in a solution containing from 10 to 300 millimolar of citric acid or biocompatible salt thereof while decreasing susceptibility to oxidative degradation of the poly(oxyalkylene)-containing polymeric material as characterized by having at least an 1.5-fold reduction of the amount of detectable formic acid and optionally other degradation by-products derived from oxidative degradation of the poly(oxyalkylene)-containing polymeric material relative to that for the poly(oxyalkylene)-containing polymeric material without citric acid or biocompatible salt thereof, wherein the biocompatible salt of citric acid is a sodium, potassium, or ammonium salt.

2. The method of claim 1 , wherein the citric acid or biocompatible salt thereof is present in an amount from 20 millimolar to 60 milimolar.

3. The method of claim 1 , wherein the solution has an osmolarity of from about 200 to 450 milli-osmole in 1000 ml (unit: mOsm/ml).

4. The method of claim 2 , wherein the solution has an osmolarity of from about 200 to 450 milli-osmole in 1000 ml (unit: mOsm/ml).

Assignments (1)
CONFIRMATORY DEED OF ASSIGNMENT EFFECTIVE APRIL 8, 2019 Recorded Dec 10, 2019
From: NOVARTIS AG
To: ALCON INC.
Reel/Frame 051454/0788 →