Claims for Patent: 8,921,337
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Summary for Patent: 8,921,337
| Title: | Carboxyvinyl polymer-containing nanoparticle suspensions |
| Abstract: | The present invention generally relates to suspension compositions having a carboxyvinyl polymer such as a carbomer, a galactomannan such as guar, and a borate compound. A sparingly soluble particulate compound such as nepafenac is also included in the compositions. The sparingly soluble particulate compound has a small particle size to enhance bioavailability of the compound. |
| Inventor(s): | Chowhan; Masood A. (Arlington, TX), Ghosh; Malay (Fort Worth, TX), Asgharian; Bahram (Arlington, TX), Han; Wesley Wehsin (Arlington, TX) |
| Assignee: | Alcon Research, Ltd. (Fort Worth, TX) |
| Application Number: | 12/957,864 |
| Patent Litigation and PTAB cases: | See patent lawsuits and PTAB cases for patent 8,921,337 |
| Patent Claims: |
1. A topically administrable aqueous ophthalmic suspension composition comprising: carbomer at a concentration of 0.1 to 0.5 w/v %; guar at a concentration of 0.1 to 0.4
w/v %; borate at a concentration of 0.4 to 2.0 w/v %; and a sparingly soluble particulate compound, said compound having a solubility in water at 25.degree. C. of 0.001 to 0.1 w/v % and a particle size of 50 to 700 nm, and wherein said sparingly
soluble particular compound is nepafenac at a concentration of 0.25 to 0.35 w/v %.
2. A composition according to claim 1, further comprising a pH-adjusting agent in an amount sufficient to cause the composition to have a pH of 5.0 to 7.2. 3. A composition according to claim 1, further comprising a tonicity-adjusting agent in an amount sufficient to cause the composition to have an osmolality of 250 to 350 mOsm/kg. 4. A composition according to claim 1 wherein said carbomer is at a concentration of 0.4 w/v %. 5. A composition according to claim 1 further comprising a milling agent at a concentration of 0.005 to 0.1 w/v %. 6. A composition according to claim 5 wherein said milling agent is a surfactant or polymer. 7. A composition according to claim 6 wherein said milling agent is sodium carboxylmethylcellulose. 8. A composition according to claim 1 further comprising a metal chloride salt tonicity-adjusting agent. 9. A composition according to claim 8 wherein said metal chloride salt is sodium chloride at a concentration of 0.4 w/v %. 10. A composition according to claim 1 further comprising a non-ionic hydroxyl compound as a tonicity-adjusting agent. 11. A composition according to claim 1 further comprising both a preservative and a chelating agent. 12. A composition according to claim 11 wherein the preservative is benzalkonium chloride at a concentration of 0.005 w/v % and the chelating agent is edetate disodium at a concentration of 0.01 w/v %. 13. A composition according to claim 1 comprising 0.4 w/v % carbomer, 0.2 w/v % guar, 0.5 w/v % boric acid, and 0.3 w/v % nepafenac. 14. A composition according to claim 13 wherein said nepafenac has an average particle size of 400 nm. 15. A topically administrable ophthalmic suspension composition consisting essentially of a) 0.3 w/v % nepafenac having a particle size of 50 to 700 nm; b) 0.4 w/v % carbomer; c) 0.2 w/v % guar; d) 0.5 w/v % boric acid; e) 0.06 w/v % sodium carboxymethylcellulose; f) 0.4 w/v % sodium chloride; g) 0.5 w/v % propylene glycol; h) a pH-adjusting agent in an amount sufficient to cause the composition to have a pH of 7.0; i) 0.005% (w/v) benzalkonium chloride; j) 0.01% edetate disodium; and k) purified water. |
