High refractive index, high Abbe compositions
US-12071497-B2 · Aug 27, 2024 · US
US9248928B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9248928-B2 |
| Application number | US-201314109978-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 18, 2013 |
| Priority date | Dec 21, 2012 |
| Publication date | Feb 2, 2016 |
| Grant date | Feb 2, 2016 |
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Contact lenses comprising an ionic component are packaged with a beneficial cationic agent in a temperature-sensitive packaging solution and/or a low ionic strength packaging solution.
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We claim: 1. A method of manufacturing a contact lens, said method comprising: a) polymerizing a monomer mixture comprising at least one carboxylic-acid containing monomer to form a lens-shaped polymerization product comprising carboxylic acid groups; b) placing the lens-shaped polymerization product in a package containing a packaging solution comprising a buffer and a beneficial cationic agent, wherein said packaging solution has an osmolality of about 200 to about 400 mOsm/kg, and wherein said packaging solution i) has an ionic strength of less than about 0.1, or ii) is temperature-sensitive, or iii) has an ionic strength of less than about 0.1 and is temperature-sensitive; and c) sealing and autoclaving the package to provide a sterile packaged contact lens, wherein the beneficial cationic agent ionically binds to the carboxylic acid groups and releases from the contact lens in an in vitro release assay; wherein at least 50% more of the cationic agent is taken up by the lens compared to an identical contact lens packaged in PBS. 2. The method of claim 1 , wherein the carboxylic-acid containing monomer is methacrylic acid. 3. The method of claim 1 , wherein the contact lens comprises from about 0.5 to about 2.5% methacrylic acid. 4. The method of claim 3 , wherein the methacrylic acid is the only ionic monomer in the monomer mixture. 5. The method of claim 1 , wherein the monomer mixture comprises a silicone monomer. 6. The method of claim 1 , wherein the monomer mixture comprises 2-hydroxyethyl methacrylate. 7. The method of claim 1 , wherein the ionic strength of the packaging solution is less than 0.1. 8. The method of claim 1 , wherein the ionic strength of the packaging solution is less than 0.06. 9. The method of claim 1 , wherein in the packaging solution comprises a non-electrolyte tonicity adjusting agent. 10. The method of claim 9 , wherein the tonicity adjusting agent is sorbitol. 11. The method of claim 1 , wherein the packaging solution has an osmolality of about 270 to about 310 mOsm/kg. 12. The method of claim 1 , wherein the cationic agent is a polymer. 13. The method of claim 1 , wherein the cationic agent is an ophthalmic drug. 14. The method of claim 1 , wherein the packaging solution comprises a temperature-sensitive buffer and the cationic agent is autoclave-stable in the packaging solution and is not autoclave-stable in PBS. 15. The method of claim 14 , wherein the temperature-sensitive buffer comprises a buffering agent selected from {[tris(hydroxymethyl)methyl]amino}propanesulfonic acid (TAPS), N,N-bis(21-hydroxyethyl)glycine (Bicine), tris(hycroxymethyl)methylamine (TRIS), N-tris(hydroxymethyl)methylglycine (Tricine), [tris(hydroxymethyl)methyl]amino}ethanesulfonic acid (TES), 3-(N-morpholino)propanesulfonic acid (MOPS), and any combination thereof. 16. The method of claim 14 , wherein the temperature-sensitive buffer comprises a TRIS buffer. 17. The method of claim 14 , wherein the cationic agent comprises a primary amine. 18. The method of claim 14 , wherein the cationic agent is epinastine and/or εPLL. 19. The method of claim 1 , further comprising storing the contact lens after it has been worn by a patient in a multi-purpose contact lens care solution (MPS) that comprises an additional amount of the cationic agent, wherein the storage solution has an osmolality of about 200 to about 400 mOsm/kg and has an ionic strength of less than about 0.1, wherein the additional cationic agent incorporates into the contact lens during the storage. 20. A contact lens made by the method of claim 1 .
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