Claims
- 1. A method for preparing submicron particles of a biologically active agent comprising the steps of:
(a) atomizing using multifluid atomization a dispersed system comprising at least one biologically active agent and at least one solvent at a mass flow ratio of about 0.30 or greater to produce droplets; (b) freezing the droplets to produce frozen droplets; (c) removing the solvent from the frozen droplets to produce friable microstructures; (d) forming a dispersion of the friable microstructures with at least one non-solvent for the biologically active agent; and (e) fragmenting the dispersed friable microstructures into submicron particles of biologically active agent.
- 2. The method of claim 1 wherein freezing is achieved by contacting the droplets with a cryogenic liquid.
- 3. The method of claim 2 wherein the cryogenic liquid is liquid nitrogen.
- 4. The method of claim 1 wherein the solvent is removed by lyophilization.
- 5. The method of claim 4 wherein lyophilization is conducted at a temperature below the lowest Tg of the frozen droplets.
- 6. The method of claim 1 wherein fragmentation is accomplished by homogenization, milling, sonication or a combination thereof.
- 7. The method of claim 6 wherein fragmentation is accomplished by sonication.
- 8. The method of claim 1 wherein the dispersion of friable microstructures further comprises at least one biocompatible polymer dissolved therein.
- 9. The method of claim 1 wherein the submicron particles have a volume median particle size of less than 1 micron, measured by laser diffraction.
- 10. The method of claim 1 wherein the biologically active agent is a protein or peptide.
- 11. The method of claim 10 wherein the protein is complexed to a stabilizing metal cation.
- 12. The method of claim 11 wherein said stabilizing metal cation is selected from the group consisting of Zn+2, Ca+2, Cu+2, Mg+2, K+ and any combination thereof.
- 13. The method of claim 12 wherein the stabilizing metal cation is Zn+2.
- 14. The method of claim 13 wherein the protein is recombinant human growth hormone.
- 15. The method of claim 1 wherein the dispersed system further comprises a metal cation component.
- 16. The method of claim 15 wherein the metal cation component is selected from the group consisting of Mg(OH)2, MgCO3, CaCO3, ZnCO3, Mg(OAc)2, Zn(OAc)2, ZnSO4, MgCl2, ZnCl2, MgSO4, zinc citrate and magnesium citrate.
- 17. A method for preparing a composition for the sustained release of biologically active agent comprising the steps of:
a) atomizing using multifluid atomization a dispersed system comprising at least one biologically active agent and at least one solvent at a mass flow ratio of about 0.30 or greater to produce droplets; b) freezing the droplets to produce frozen droplets; c) removing the solvent from the frozen droplets to produce friable micro structures; d) dispersing the friable microstructures in at least one non-solvent for the biologically active agent; e) fragmenting the dispersed friable microstructures to produce submicron particles of the biologically active agent; f) providing a suspension comprising the submicron particles of the biologically active agent, at least one biocompatible polymer and at least one polymer solvent; and g) removing the polymer solvent to form a solid polymer/active agent matrix.
- 18. The method of claim 17 further comprising the steps of:
a) forming droplets of the polymer/active agent suspension; b) freezing the droplets of the polymer/active agent suspension wherein steps a) and b) are performed prior to removing the polymer solvent; and c) removing the polymer solvent by extraction with an extraction solvent.
- 19. The method of claim 17 wherein the submicron particles have a volume median particle size of less than 1 micron, measured by laser diffraction.
- 20. The method of claim 17 wherein the biologically active agent is present in the suspension at a concentration of from about 0.01 to about 50% w/w of the combined weight of polymer and biologically active agent.
- 21. The method of claim 20 wherein the biologically active agent is present at a concentration of about 0.01 to 30% w/w of the combined weight of the polymer and biologically active agent.
- 22. The method of claim 17 wherein the biologically active agent is a protein or peptide.
- 23. The method of claim 22 wherein the biologically active agent is complexed to a stabilizing metal cation.
- 24. The method of claim 23 wherein said stabilizing metal cation is selected from the group consisting of Zn+2, Ca+2, Cu+2, Mg+2, K+ and any combination thereof.
- 25. The method of claim 24 wherein said stabilizing metal cation is Zn+2.
- 26. The method of claim 22 wherein the protein is human growth hormone.
- 27. The method of claim 26 wherein the human growth hormone is complexed to Zn+2.
- 28. The method of claim 17 wherein the biocompatible polymer is biodegradable.
- 29. The method of claim 28 wherein the biodegradable polymer is selected from the group consisting of poly(lactide)s, poly(glycolide)s, poly(lactide-coglycolide)s, poly(lactic acid)s, poly(glycolic acid)s, poly(lactic acid-co-glycolic acid)s, poly(caprolactone), polycarbonates, polyesteramides, polyanhydrides, poly(amino acid)s, poly(ortho ester)s, polycyanoacrylates, polyamides, polyacetals, poly(ether ester)s, copolymers of poly(ethylene glycol) and poly(ortho ester)s, poly(dioxanone)s, poly(alkylene alkylate)s, biodegradable polyurethanes, blends and copolymers thereof.
- 30. The method of claim 29 wherein said polymer is poly(lactide-co-glycolide).
- 31. The method of claim 17 wherein the biocompatible polymer is non-biodegradable.
- 32. The method of claim 17 wherein the polymer solvent is methylene chloride, chloroform, acetone, ethyl acetate, methyl acetate, dimethylsulfoxide, hexafluoroisopropanol or any combinations thereof.
- 33. The method of claim 17 wherein the dispersed system further comprises a metal cation component which modulates the release of the biologically active agent from the composition for sustained release.
- 34. The method of claim 33 wherein the metal cation component is selected from the group consisting of Mg(OH)2, MgCO3, CaCO3, ZnCO3, Mg(OAc)2, Zn(OAc)2, ZnSO4, MgCl2, ZnCl2, MgSO4, zinc citrate and magnesium citrate.
- 35. The method of claim 17 wherein the suspension further comprises a metal cation component which modulates the release of the biologically active agent from the composition for sustained release.
- 36. A method for providing a therapeutically, prophylactically or diagnostically effective amount of a biologically active agent to a subject in need thereof for a sustained period comprising administering to the subject a dose of the sustained release composition prepared according to claim 17.
- 37. Submicron particles of biologically active agent prepared according to a method comprising the steps of:
(a) atomizing using multifluid atomization a dispersed system comprising at least one biologically active agent and at least one solvent at a mass flow ratio of about 0.30 or greater to produce droplets; (b) freezing the droplets to produce frozen droplets; (c) removing the solvent from the frozen droplets to produce friable microstructures; (d) forming a dispersion of the friable microstructures with at least one non-solvent for the biologically active agent; and (e) fragmenting the dispersed friable microstructures into submicron particles of biologically active agent.
- 38. The submicron particles of claim 37 wherein freezing is achieved by contacting the droplets with a cryogenic liquid.
- 39. The submicron particles of claim 38 wherein the cryogenic liquid is liquid nitrogen.
- 40. The submicron particles of claim 37 wherein the solvent is removed by lyophilization.
- 41. The submicron particles of claim 40 wherein lyophilization is conducted at a temperature below the lowest Tg of the frozen droplets.
- 42. The submicron particles of claim 37 wherein fragmentation is accomplished by homogenization, milling, sonication or a combination thereof.
- 43. The submicron particles of claim 42 wherein fragmentation is accomplished by sonication.
- 44. The method of claim 37 wherein the dispersion of friable microstructures further comprises at least one biocompatible polymer dissolved therein.
- 45. The submicron particles of claim 37 wherein the submicron particles have a volume median particle size of less than 1 micron, measured by laser diffraction.
- 46. The submicron particles of claim 37 wherein the biologically active agent is a protein or peptide.
- 47. The submicron particles of claim 46 wherein protein is complexed to a stabilizing metal cation.
- 48. The submicron particles of claim 47 wherein said stabilizing metal cation is selected from the group consisting of Zn+2, Ca+2, Cu+2, Mg+2, K+ and any combination thereof.
- 49. The submicron particles of claim 48 wherein the stabilizing metal cation is zinc.
- 50. The submicron particles of claim 49 wherein the protein is recombinant human growth hormone.
- 51. The submicron particles of claim 37 wherein the dispersed system further comprises a metal cation component.
- 52. The submicron particles of claim 51 wherein the metal cation component is selected from the group consisting of Mg(OH)2, MgCO3, CaCO3, ZnCO3, Mg(OAc)2, Zn(OAc)2, ZnSO4, MgCl2, ZnCl2, MgSO4, zinc citrate and magnesium citrate.
RELATED APPLICATION(S)
[0001] This application is a continuation of application Ser. No. 09/422,751, filed Oct. 21, 1999. The entire teachings of the above application are incorporated herein by reference.
Continuations (1)
|
Number |
Date |
Country |
Parent |
09422751 |
Oct 1999 |
US |
Child |
09898524 |
Jul 2001 |
US |