Controlled release microencapsulated NGF formulation

• US 6,663,899 B2
• Filed: 06/11/1998
• Issued: 12/16/2003
• Est. Priority Date: 06/13/1997
• Status: Expired due to Term

• Current Assignee: Genentech, Inc. (Roche Holding AG)
• Original Assignee: Genentech, Inc. (Roche Holding AG)
• Inventors: Duenas, Eileen T., Lam, Xanthe M., Cleland, Jeffrey L.
• Primary Examiner(s): Kunz, Gary
• Assistant Examiner(s): HAYES, ROBERT CLINTON
• Application Number:
  US09/095,911
• Publication Number:
  US 20020004481A1
• Time in Patent Office: 2,014 Days
• Field of Search: 514/2, 514/12, 514/773, 424/600, 424/641, 424/625, 424/630, 424/646, 424/650, 424/610, 424/611, 424/602, 424/682, 424/489, 424/491, 530/399
• US Class Current: 424/491
• CPC Class Codes: A61K 38/185 Nerve growth factor [NGF]; Brain derived neurotrophic factor [BDNF]; Ciliary neurotrophic factor [CNTF]; Glial derived neurotrophic factor [GDNF]; Neurotrophins, e.g. NT-3
• CPC Class Codes: A61K 9/1647 Polyesters, e.g. poly(lactide-co-glycolide)
• CPC Class Codes: C07K 14/48 Nerve growth factor [NGF]

Abstract

NGF microencapsulation compositions having controlled release characteristics, preferably with increased stability, for the NGF component, particularly human recombinant NGF (“rhNGF”) are provided that yield enhanced stability of NGF for use in promoting nerve cell growth, repair, survival, differentiation, maturation or function. Methods for making and using such compositions are also provided.

Claims

1. A method of making a biodegradable polymeric microsphere device for controlled sustained release of NGF, comprising mixing NGF in solution with an NGF-stabilizing metal salt, a biodegradable polymer, and microencapsulating the NGF-metal mixture to form a metal salt stabilized microsphere with a particle size from about 0.1 to about 300 μ

m, wherein said microsphere contains NGF and metal capable of controlled sustained release of NGF for a period of time greater than one day, and wherein said NGF promotes basal forebrain cholinergic neuron outgrowth.

2. The method of claim 1, wherein the molar ratio of NGF to metal in the solution is 1 to 6 to 1 to 20.

3. The method of claim 2, wherein the molar ratio of NGF to metal in the solution is 1 to 8 to 1 to 14.

4. The method of claim 2, wherein the metal is an alkali metal, alkaline earth metal, or polyvalent metal.

5. The method of claim 4, wherein the metal is sodium, potassium, calcium, magnesium, iron II, iron III, copper II, tin II, tin IV, aluminum II, aluminum III, or zinc.

6. The method of claim 4, wherein the metal is zinc.

7. The method of claim 1, wherein the metal is in an aliphatic carboxylic acid salt form.

8. The method of claim 7, wherein the salt is a carbonate or acetate salt.

9. The method of claim 1, wherein the metal salt is zinc chloride, zinc bromide, zinc iodide, zinc fluoride, zinc sulfate, zinc nitrate, zinc thiocyanate, zinc carbonate, zinc acetate, zinc glycolate, zinc lactate, zinc tartrate, zinc benzoate, zinc salicylate, zinc phenolsulfonate, calcium chloride, calcium bromide, calcium iodide, calcium fluoride, calcium sulfate, calcium nitrate, calcium thiocyanate, calcium carbonate, calcium acetate, calcium propionate, calcium oxalate, calcium tartrate, calcium lactate, calcium citrate, calcium gluconate, calcium benzoate, or calcium salicylate.

10. The method of claim 9, wherein the metal salt is zinc acetate, zinc carbonate, calcium acetate, or calcium carbonate.

11. The method of claim 1, wherein the NGF is human 118 NGF.

12. The method of claim 1 wherein the mixture is pH 6 to 8.

13. The method of claim 1, further comprising admixing a polyol stabilizer having a molecular weight of less than about 70,000 kD.

14. The method of claim 13, wherein the polyol is a sugar alcohol.

15. The method of claim 14, wherein the sugar is trehalose, mannitol, or sucrose.

16. The method of claim 1, further comprising drying the NGF-metal solution prior to admixing with the biodegradable polymer.

17. The method of claim 1, further comprising admixing a release modifier into the dried NGF-metal mixture or NGF-biodegradable polymer mixture.

18. The method of claim 1, wherein the microencapsulation comprises drying the NGF-metal solution, dispersing the biodegradable polymer in an organic solvent, admixing the dried NGF mixture with the biodegradable polymer organic solvent mixture, spraying the NGF-biodegradable polymer mixture to form droplets, removing the organic solvent from the droplets to form microspheres containing NGF.

19. The method of claim 18, which further comprises admixing a release modifier with the dried NGF-metal mixture.

20. The method of claim 18, wherein the organic solvent is ethyl acetate or methylene chloride.

21. The method of claim 1, wherein the NGF is 5 to 20% by weight in the microsphere.

22. The method of claim 1, wherein the biodegradable polymer is polylactide or poly(lactide-co-glycolide).

23. The method of claim 1, further comprising compressing the microspheres to form a pellet.

24. A biodegradable polymeric microsphere device having a diameter of about 0.1 to about 300 μ

m for sustained controlled release of NGF for a period of time greater than one day, comprising a biodegradable polymeric microsphere containing 0.1 to 50% NGF by weight made by the method of claim 1, and wherein said NGF promotes basal forebrain cholinergic neuron outgrowth.

26. The method of claim 1, wherein the molar ratio of NGF to metal is 1 to 4 to 1 to 50.

27. The method of claim 1, wherein said period of time is at least 1 week.

28. The method of claim 1, wherein said particle size is from about 1 to about 150 μ

m.

29. The method of claim 1, wherein said particle size is from about 2 to about 100 μ

m.

30. The method of claim 1, wherein said particle size is from about 20 to about 90 μ

m.

31. The device of claim 24, wherein said period of time is at least 1 week.

25. A method of increasing the stability of NGF in a biodegradable microencapsulated composition, comprising incorporating an NGF-stabilizing metal salt into an NGF aqueous biodegradable polymer-containing solution prior to drying the solution for microencapsulation, whereby microspheres capable of releasing NGF over a period of time in excess of one day are produced, and wherein said NGF promotes basal forebrain cholinergic neuron outgrowth.