Contact lens packaging solutions containing hydrophilic polymers endcapped with a hydrophilic and a hydrophobic group
A packaging system for the storage of an ophthalmic device is disclosed. The packaging system comprises a sealed container containing one or more unused ophthalmic devices immersed in an aqueous packaging solution comprising one or more hydrophilic polymers or copolymers comprising hydrophilic units and endcapped with a hydrophobic end group and a hydrophilic end group, wherein the solution has an osmolality of at least about 200 mOsm/kg, a pH of about 6 to about 9 and is heat sterilized.
1. A packaging system for the storage of an ophthalmic device comprising a sealed container containing one or more unused ophthalmic devices immersed in an aqueous packaging solution comprising one or more hydrophilic polymers or copolymers comprising hydrophilic units, the one or more hydrophilic polymers or copolymers having a hydrophobic terminal end group and a hydrophilic terminal end group, wherein the aqueous packaging solution has an osmolality of at least about 200 mOsm/kg, a pH of about 6 to about 9 and is heat sterilized.
2. The packaging system of claim 1 , wherein the ophthalmic device is a contact lens.
3. The packaging system of claim 1 , wherein the hydrophilic units are derived from at least one ethylenically unsaturated polymerizable hydrophilic monomer.
4. The packaging system of claim 3 , wherein the at least one ethylenically unsaturated polymerizable hydrophilic monomer is selected from the group consisting of an acrylamide, an acetamide, a formamide, a cyclic lactam, a (meth)acrylated alcohol, a (meth)acrylated poly(alkyleneoxy), an ethylenically unsaturated carboxylic acid, a hydrophilic vinyl carbonate, a hydrophilic vinyl carbamate, a hydrophilic oxazolone monomer, and mixtures thereof.
5. The packaging system of claim 1 , wherein the hydrophilic terminal end group of the one or more hydrophilic polymers or copolymers is —OH or —CN.
6. The packaging system of claim 1 , wherein the hydrophilic terminal end group of the one or more hydrophilic polymers or copolymers is an end hydrophilic unit of the hydrophilic units.
7. The packaging system of claim 1 , wherein the hydrophilic units comprise from about 10 to about 3000 units.
8. The packaging system of claim 1 , wherein the one or more hydrophilic polymers or copolymers are derived from reversible addition fragmentation chain transfer (RAFT) polymerization.
9. The packaging system of claim 1 , wherein the hydrophobic terminal end group is selected from the group consisting of a straight or branched C 3 to C 18 alkyl group, a C 3 to C 30 cycloalkyl group, a C 6 to C 30 aryl group, a C 7 to C 30 arylalkyl group, a fluorine substituted straight or branched C 3 to C 18 alkyl group, a fluorine substituted C 3 to C 30 cycloalkyl group, a fluorine substituted C 6 to C 30 aryl groups, a fluorine substituted C 7 to C 30 arylalkyl group, a polydimethylsiloxane and an organosilicon-containing monomer.
10. The packaging system of claim 1 , wherein the one or more hydrophilic polymers or copolymers have a number average molecular weight ranging from about 1,500 Da to about 75,000 Da.
11. The packaging system of claim 1 , wherein a concentration of the one or more hydrophilic polymers or copolymers in the aqueous packaging solution ranges from about 0.01% to about 10% w/w.
12. The packaging system of claim 1 , wherein a concentration of the one or more hydrophilic polymers or copolymers in the aqueous packaging solution ranges from about 0.1 to about 5% w/w.
13. The packaging system of claim 1 , wherein the aqueous packaging solution further comprises a buffer agent, a tonicity adjusting agent, a cleaning agent, a wetting agent, a nutrient agent, a sequestering agent, a viscosity builder, a contact lens conditioning agent, an antioxidant, and mixtures thereof.
14. The packaging system of claim 1 , wherein the sealed container is heat sterilized subsequent to sealing of the container and the aqueous packaging solution does not contain an effective disinfecting amount of a disinfecting agent or a germicide compound.
15. The packaging system of claim 1 , wherein the aqueous packaging solution does not contain an effective disinfecting amount of a disinfecting agent.
16. The packaging system of claim 1 , wherein the aqueous packaging solution does not contain a germicide compound.
17. A method of preparing a packaging system comprising a storable, sterile ophthalmic device, the method comprising:
(a) providing an ophthalmic device;
(b) immersing the ophthalmic device in an aqueous packaging solution comprising one or more hydrophilic polymers or copolymers comprising hydrophilic units, the one or more hydrophilic polymers or copolymers having a hydrophobic terminal end group and a hydrophilic terminal end group, wherein the aqueous packaging solution has an osmolality of at least about 200 mOsm/kg and a pH in the range of about 6 to about 9;
(c) packaging the aqueous packaging solution and the ophthalmic device in a manner preventing contamination of the ophthalmic device by microorganisms; and
(d) sterilizing the packaged solution and the ophthalmic device.
18. The method of claim 17 , wherein the ophthalmic device is a contact lens.
19. The method of claim 17 , wherein the hydrophilic units are derived from at least one ethylenically unsaturated polymerizable hydrophilic monomer selected from the group consisting of an acrylamide, an acetamide, a formamide, a cyclic lactam, a (meth)acrylated alcohol, a (meth)acrylated poly(alkyleneoxy), an ethylenically unsaturated carboxylic acid, a hydrophilic vinyl carbonate, a hydrophilic vinyl carbamate, a hydrophilic oxazolone monomer, and mixtures thereof.
20. The method of claim 17 , wherein the hydrophilic terminal end group of the one or more hydrophilic polymers or copolymers is —OH and —CN.
21. The method of claim 17 , wherein the hydrophilic terminal end group of the one or more hydrophilic polymers or copolymers is an end hydrophilic unit of the hydrophilic units.
22. The method of claim 17 , wherein the hydrophilic units comprise from about 10 to about 3000 units.
23. The method of claim 17 , wherein the one or more hydrophilic polymers or copolymers are derived from reversible addition fragmentation chain transfer (RAFT) polymerization.
24. The method of claim 17 , wherein the hydrophobic terminal end group is selected from the group consisting of a straight or branched C 3 to C 18 alkyl group, a C 3 to C 30 cycloalkyl group, a C 6 to C 30 aryl group, a C 7 to C 30 arylalkyl group, a fluorine substituted straight or branched C 3 to C 18 alkyl group, a fluorine substituted C 3 to C 30 cycloalkyl group, a fluorine substituted C 6 to C 30 aryl groups, a fluorine substituted C 7 to C 30 arylalkyl group, a polydimethylsiloxane and an organosilicon-containing monomer.
25. The method of claim 17 , wherein the one or more hydrophilic polymers or copolymers have a number average molecular weight ranging from about 1,500 Da to about 75,000 Da.
26. The method of claim 17 , wherein a concentration of the one or more hydrophilic polymers or copolymers in the aqueous packaging solution ranges from about 0.01% to about 10% w/w.
27. The method of claim 17 , wherein the aqueous packaging solution further comprises a buffer agent, a tonicity adjusting agent, a cleaning agent, a wetting agent, a nutrient agent, a sequestering agent, a viscosity builder, a contact lens conditioning agent, an antioxidant, and mixtures thereof.
28. The method of claim 17 , wherein sterilizing the packaged solution and the ophthalmic device comprises heat sterilizing the packaged solution and the ophthalmic device, and the aqueous packaging solution does not contain an effective disinfecting amount of a disinfecting agent or a germicide compound.