Claims for Patent: 11,826,347

Summary for Patent: 11,826,347

Title:	Anesthetic composition and method of anesthetizing the eye
Abstract:	A topical ophthalmic anesthetic composition includes a formulation with an amount of articaine to provide anesthetic properties when applied topically to the eye, and a pH, viscosity, osmolality, dissociation constant, and additives such as antioxidants, buffers, methylcellulose, to achieve efficacy and safety. The composition can contain articaine in amounts of about 4.0% w/v to about 12.0% w/v and have a pH of about pH 3.5 to pH 7.0. The buffer can be borate/mannitol complex obtained from boric acid or salt thereof and D-mannitol. The articaine formulations can achieve adequate anesthesia of the internal aspect of the eye wall by topical application, without the use of an injectable anesthetic. Exemplary implementations of the disclosure include formulations include articaine in an amount of at least 7.0% w/v, where the formulation is an aqueous solution, a gel, an ointment, or in an encapsulated form.
Inventor(s):	Martin Uram
Assignee:	American Genomics LLC
Application Number:	US17/381,844
Patent Claims:	1. An aqueous topical ophthalmic anesthetic composition comprising: articaine in an amount of about 4.0% w/v to about 13.0% w/v based on the volume of the composition; and a buffer in an amount to provide a pH of about pH 3.5 to about pH 7.0, where said buffer is non-reactive with and stabilizes articaine to inhibit degradation of said articaine during storage, where said composition has an osmolality of 275 to 1171 mOsm/kg to facilitate topical application for ophthalmic anesthesia, and where said buffer is present in an amount to stabilize and inhibit degradation of said articaine. 2. The composition of claim 1, wherein said composition has a pH of about pH 4.5 to about pH 5.5, and where said buffer comprises a complex obtained from a citrate, acetate or mixture thereof and a sugar alcohol selected from the group consisting of mannitol, sorbitol and mixtures thereof. 3. The composition of claim 1, wherein said composition comprises about 7.5% w/v to 8.5% w/v articaine and said composition has a pH of about pH 4.5 to about pH 5.0. 4. The composition of claim 1, wherein said composition contains at least about 7.0% w/v articaine and has a pH of about pH 4.5 to about pH 5.0. 5. The composition of claim 1, wherein said buffer comprises a borate/mannitol complex obtained from a borate and D-mannitol. 6. The composition of claim 5, wherein said borate/mannitol complex is included in an amount of about 0.5% w/v to about 0.75% w/v based on the volume of the composition. 7. The composition of claim 5, wherein said borate/mannitol complex is included in an amount of about 6.5 parts by weight to about 7.5 parts by weight based on 100 parts by weight of articaine in the composition. 8. The composition of claim 5, wherein said borate/mannitol complex is obtained from a borate/mannitol ratio of about 1:3 to about 1:7 by weight. 9. The composition of claim 5, wherein said composition further includes sodium acetate, acetic acid, and disodium edetate. 10. The composition of claim 1, wherein said composition comprises at least about 7.0% w/v articaine and said buffer comprises a complex of boric acid and D-mannitol in an amount to provide a pH of about pH 4.5 to about pH 5.0 and said composition further comprises sodium acetate, acetic acid, and disodium edetate. 11. The composition of claim 4, wherein said articaine is present in an amount of at least about 7.0% w/v, and said boric acid and D-mannitol complex is obtained from about 0.08% w/v to about 0.10% w/v boric acid and about 0.50% w/v to about 0.6% w/v D-mannitol based on the total volume of the composition. 12. The composition of claim 1, wherein said composition comprises at least about 8.0% w/v articaine, a buffer complex obtained from about 0.08% w/v to about 0.10% w/v boric acid and about 0.5% w/v to about 0.60% w/v D-mannitol, about 0.3 to 0.36% w/v sodium acetate, about 0.05% w/v to about 0.07% w/v disodium edetate, and the balance water, and where said composition has an osmolality of about 280 to 320 mOsm/kg and the amounts are based on the total volume of the composition. 13. The composition of claim 1, wherein said composition comprises about 4% w/v articaine, and said buffer comprises NaOH and HCl, and said composition has a pH of about pH 5.5, a pKa of about 7.8, a viscosity of about 20-25 cp, an osmolality of about 275 to 1171 mOsm/kg, and a tonicity of about 0.5 to 5.0%. 14. The composition of claim 1, wherein said composition comprises 80 mg/g articaine HCl, 1.373 mg/g sodium phosphate monobasic monohydrate, 1.413 mg/g sodium phosphate dibasic anhydrous, 8.1 mg/g hydroxypropylmethyl cellulose, 4 mg/g PEG400, and where said composition has a pH of pH 6.0 to pH 7.0, a viscosity of 743-803 cp, and an osmolality of 517 mOsm/kg. 15. An aqueous topical ophthalmic anesthetic composition comprising: articaine in an amount of about 4.0% to about 13% w/v based on the volume of the composition; and a buffer in an amount to provide a pH of pH 3.5 to 7.0 to inhibit irritation to an ocular surface and to stabilize articaine during storage, and where said buffer is a complex obtained from a boric acid or a boric acid salt and a sugar alcohol in an amount to maintain said articaine in solution or suspension and inhibit degradation of said articaine during storage. 16. The aqueous ophthalmic anesthetic composition of claim 15, wherein said buffer is a borate/mannitol complex in an amount of about 6.5 parts by weight to about 7.5 parts by weight based on 100 parts by weight of articaine in the composition. 17. The aqueous ophthalmic anesthetic composition of claim 16, wherein said borate/mannitol complex is obtained from a borate/mannitol ratio of about 1:3 to about 1:7 by weight. 18. The aqueous ophthalmic anesthetic composition of claim 17, further comprising sodium diacetate, acetic acid, and disodium edetate. 19. A method of providing anesthesia to the eye, the method comprising the step of topically applying the composition of claim 1 to the surface of the eye of a patient in an amount effective to anesthetize the eye of the patient. 20. The method of claim 19, wherein said composition comprises articaine in an amount of at least about 5.0%, said buffer complex obtained from about 0.08% w/v to about 0.10% w/v boric acid and about 0.50% w/v to about 0.6% w/v D-mannitol based on the total volume of the composition. 21. The method of claim 19, wherein said composition comprises at least about 7.5% w/v articaine; a buffer including a complex obtained from boric acid and D-mannitol in an amount that is non-reactive with articaine; sodium acetate; acetic acid; disodium edetate, and the balance water, and where said composition has a pH of about pH 4.5 to about pH 5.5. 22. The method of claim 19, wherein said composition comprises at least about 7% w/v articaine. 23. The method of claim 22, wherein said composition has a pH of about pH 4.5 to about pH 5.0. 24. The method of claim 19, wherein said formulation comprises 4% w/v articaine, has a pH 5.5, a pKa of 7.8, a viscosity of 20-25 cp, an osmolality of 275-1171 mOsms/kg, a tonicity of 0.5%-5.0%, a NaOH buffer, and a HCl buffer. 25. The method of claim 19, wherein said composition comprises 80 mg/g articaine HCl, 1.373 mg/g sodium phosphate monobasic monohydrate, 1.413 mg/g sodium phosphate dibasic anhydrous, 8.1 mg/g hydroxypropylmethyl cellulose, 4 mg/g PEG400, and where said composition has a pH of pH 6.0 to pH 7.0, a viscosity of 743-803 cp, and an osmolality of 517 mOsm/kg. 26. A method of producing the composition of claim 1, comprising the steps of: mixing an acid or salt thereof and a sugar alcohol in a solution to form a buffer complex; adjusting the pH to about 3.5 to about pH 7.0; and adding articaine to the resulting solution in an amount to obtain said composition having about 4.0% w/v to about 13% w/v based on the volume of the composition, and stabilizing said composition by including an amount of said buffer complex to maintain said articaine in solution or suspension and to inhibit degradation of said articaine during storage. 27. The method of claim 26, wherein said acid is selected from the group consisting of acetic acid, citric acid, and mixtures thereof, and said sugar alcohol is selected from the group consisting of D-mannitol, sorbitol, and mixtures thereof. 28. The method of claim 26, wherein said acid or salt thereof is a borate salt and said sugar alcohol is D-mannitol, and said complex is a borate/mannitol complex, and where said composition comprises at least 7.0% articaine, and has a pH of about pH 6.0 to pH 7.0. 29. The method of claim 28, wherein said borate/mannitol complex is obtained from a borate/mannitol ratio of about 1:3 to about 1:7 by weight. 30. The composition of claim 15, wherein said composition has an osmolality of 500 to 700 mOsms/kg. 31. The composition of claim 30, wherein said composition has a pH of 4.5 to 7.0. 32. The composition of claim 31, wherein said composition contains 7.5% to 8.8% w/v articaine. 33. The composition of claim 30, wherein said composition has an osmolality of 580 to 630 mOsms/kg.