Liposomal formulation for ocular drug delivery

Patent metadata

Field	Value
Publication number	US-10272040-B2
Application number	US-201113816640-A
Country	US
Kind code	B2
Filing date	Aug 12, 2011
Priority date	Aug 12, 2010
Publication date	Apr 30, 2019
Grant date	Apr 30, 2019

Abstract

The present invention is directed to a liposomal formulation for ocular drug delivery comprising (i) liposomes comprising at least one lipid bilayer, and (ii) a prostaglandin drug and/or a prostaglandin derivative associated in the liposomes, wherein the liposomes have a mean diameter of less than 2μπι. The present invention is also directed to a pharmaceutical comprising the liposomal formulation and a method of producing the liposomal formulation for ocular drug delivery. Additionally, the present invention is directed to a method of treating or preventing an ocular disease, comprising administering the liposomal formulation or the pharmaceutical composition to a subject in need thereof.

First claim

The Invention claimed is:

1. A liposomal formulation for ocular drug delivery comprising:
(i) liposomes comprising at least one lipid bilayer; and
(ii) latanoprost encapsulated in the liposomes,

wherein the liposomes have a mean diameter of 100 nm to 300 nm, the liposomes comprise phosphatidylcholine, the liposomal formulation is a sustained release formulation having a latanoprost to lipid mole ratio of 0.01:1 to 0.50:1, less than 60% of the latanoprost encapsulated in the liposomes is released from the liposomes in 10 days, as measured by an in vitro release assay, and egg phosphatidylcholine is the only phosphatidylcholine in the liposomal formulation.

2. The liposomal formulation as claimed in claim 1 , wherein the liposomal formulation has a latanoprost to lipid mole ratio of 0.01:1 to 0.37:1.

3. The liposomal formulation as claimed in claim 2 , wherein the liposomal formulation has a latanoprost to lipid mole ratio of 0.015:1 to 0.37:1.

4. The liposomal formulation as claimed in claim 3 , wherein the liposomal formulation has a latanoprost to lipid mole ratio of 0.04:1 to 0.37:1.

5. The liposomal formulation as claimed in claim 1 , wherein the liposomes further comprise at least one sphingolipid, sterol lipid, saccharolipid, or polyketide lipid.

6. The liposomal formulation as claimed in claim 5 , wherein the sphingolipid comprises at least one unsaturated fatty acid moiety.

7. The liposomal formulation as claimed in claim 6 , wherein the sphingolipid comprises hexadecanoylsphingomyelin or egg sphingomyelin.

8. The liposomal formulation as claimed in claim 1 , wherein the liposomal formulation has a latanoprost to lipid mole ratio of 0.50:1.

9. The liposomal formulation as claimed in claim 1 , wherein the liposomal formulation has a latanoprost to lipid mole ratio of 0.18:1.

10. The liposomal formulation as claimed in claim 1 , wherein the liposomal formulation has a polydispersity index of less than or equal to 0.25.

11. The liposomal formulation as claimed in claim 1 , wherein the liposomes further comprise cholesterol.

12. The liposomal formulation as claimed in claim 11 , wherein the cholesterol is of an amount of about 10% to about 40% by weight of the liposomes.

13. The liposomal formulation as claimed in claim 1 , wherein the liposomes further comprise a linear C 8 -C 20 alkyl or alkenyl amine.

14. The liposomal formulation as claimed in claim 13 , wherein the linear C 8 -C 20 alkyl or alkenyl amine is stearyl amine.

15. The liposomal formulation as claimed in claim 14 , wherein the stearyl amine is present at 5% to 25% by weight of the liposomes.

16. The liposomal formulation as claimed in claim 15 , wherein the stearyl amine is present at 10% to 20% by weight of the liposomes.

17. A pharmaceutical composition comprising a sustained release liposomal formulation comprising:
(i) liposomes comprising at least one lipid bilayer; and
(ii) latanoprost encapsulated in the liposomes,

wherein the liposomes have a mean diameter of 100 nm to 300 nm, the liposomes comprise phosphatidylcholine, the liposomal formulation has a latanoprost to lipid mole ratio of 0.01:1 to 0.50:1, less than 60% of the latanoprost encapsulated in the liposomes is released from the liposomes in 10 days, as measured by an in vitro release assay, and egg phosphatidylcholine is the only phosphatidylcholine in the liposomal formulation.

18. The pharmaceutical composition as claimed in claim 17 , wherein the liposomal formulation has a latanoprost to lipid mole ratio of 0.01:1 to 0.37:1.

19. The pharmaceutical composition as claimed in claim 17 , wherein the liposomal formulation has a latanoprost to lipid mole ratio of 0.015:1 to 0.37:1.

20. The pharmaceutical composition as claimed in claim 19 , wherein the liposomal formulation has a latanoprost to lipid mole ratio of 0.04:1 to 0.37:1.

21. The pharmaceutical composition as claimed in claim 17 , wherein the pharmaceutical composition is in the form of an ophthalmic solution.

22. The pharmaceutical composition as claimed in claim 17 , wherein the pharmaceutical composition is formulated for ocular drug delivery as an injection solution or a viscous aqueous vehicle.

23. The pharmaceutical composition as claimed in claim 17 , wherein the pharmaceutical composition is formulated for ocular drug delivery as a viscous aqueous vehicle, wherein the viscous aqueous vehicle comprises an aqueous solution of a polysaccharide.

24. The pharmaceutical composition as claimed in claim 23 , wherein the polysaccharide is hyaluronic acid.

25. A method for treating an ocular disease, comprising administering a sustained release liposomal formulation to the eye of a subject in need thereof, the liposomal formulation comprising:
(i) liposomes comprising at least one lipid bilayer; and
(ii) latanoprost encapsulated in the liposomes,

wherein the ocular disease is glaucoma, the liposomes have a mean diameter of 100 nm to 300 nm, the liposomes comprise phosphatidylcholine, the liposomal formulation has a latanoprost to lipid mole ratio of 0.01:1 to 0.50:1, less than 60% of the latanoprost encapsulated in the liposomes is released from the liposomes in 10 days, as measured by an in vitro release assay, and egg phosphatidylcholine is the only phosphatidylcholine in the liposomal formulation.

26. The method as claimed in claim 25 , wherein the liposomal formulation is administered by subconjunctival injection.

Assignees

• Venkatraman Subramanian
• Natarajan Jayaganesh V
• Wong Tina
• Boey Yin Chiang Freddy
• Univ Nanyang Tech
• Singapore Health Serv Pte Ltd

Inventors

• Venkatraman Subramanian
• Natarajan Jayaganesh V
• Wong Tina
• Boey Yin Chiang Freddy

Classifications

• A61K31/5575

  having a cyclopentane, e.g. prostaglandin E2, prostaglandin F2-alpha · CPC title

• A61K31/215

  of carboxylic acids · CPC title

• A61K9/127 Primary

  Synthetic bilayered vehicles, e.g. liposomes or liposomes with cholesterol as the only non-phosphatidyl surfactant · CPC title

• A61K9/0048

  Eye, e.g. artificial tears · CPC title