Production of microcapsules of water-soluble drugs

• US 5,611,971 A
• Filed: 08/06/1993
• Issued: 03/18/1997
• Est. Priority Date: 08/07/1992
• Status: Expired due to Term

• Current Assignee: Takeda Pharmaceutical Company Limited
• Original Assignee: Takeda Chemical Industries, Ltd. (Takeda Pharmaceutical Company Limited)
• Inventors: Futo, Tomomichi, Hori, Masuhisa, Maedera, Koichi
• Primary Examiner(s): Nutter, Nathan M.
• Application Number:
  US08/102,790
• Time in Patent Office: 1,320 Days
• Field of Search: 264/4.6, 264/4.1
• US Class Current: 264/4.1
• CPC Class Codes: A61K 9/1647 Polyesters, e.g. poly(lactide-co-glycolide)
• CPC Class Codes: A61K 9/1694 resulting in granules or microspheres of the matrix type containing more than 5% of excipient

Abstract

There is provided a process for producing microcapsules of a water-soluble drug by in-water drying process, which comprises carrying out the process in the presence of an osmotic pressure adjustor present in the external aqueous phase. This process improves the drug take up into microcapsules.

Claims

1. A process for producing microcapsules of a water-soluble drug by in-water drying process, which comprises carrying out the process in the presence of an osmotic pressure adjustor present in the external aqueous phase, wherein the concentration of the osmotic pressure adjustor in the external aqueous phase is about 0.001 to about 60% (w/w), and wherein the osmotic pressure adjustor is selected from the group consisting of water-soluble polyhydric alcohols, water-soluble monohydric alcohols, water-soluble monosaccharides, water-soluble disaccharides, water-soluble oligosaccharides and their derivatives, and water-soluble amino acids and their salts.

2. A process according claim 1 which comprises (1) preparing a W/O emulsion whose internal aqueous phase is a solution containing a water-soluble drug and whose oil phase is a solution containing a polymer, (2) dispersing the W/O emulsion in a solution or suspension for the aqueous phase containing an osmotic pressure adjustor to prepare a (W/O)/W emulsion, and (3) subjecting the (W/O)/W emulsion to in-water drying process.

3. A process according to claim 1 which comprises (1) dispersing a solution or suspension for the oil phase comprising a water-soluble drug and a polymer in a solution or suspension for the aqueous phase containing an osmotic pressure adjustor to prepare an O/W emulsion, and (2) subjecting the O/W emulsion to in-water drying process.

4. A process according to claim 1 wherein the water-soluble drug is a peptide having biological activities.

5. A process according to claim 4, wherein the molecular weight of the polypeptide is about 200 to about 80,000 daltons.

6. A process according to claim 4 wherein the peptide having biological activities is thyrotropin-releasing hormone.

7. A process according to claim 1 wherein the osmotic pressure adjustor is a water-soluble polyhydric alcohol.

8. A process according to claim 1 wherein the osmotic pressure adjustor is a water-soluble hexahydric alcohol.

9. A process according to claim 1 wherein the osmotic pressure adjustor is mannitol.

10. A process according to claim 1 wherein the concentration of the osmotic pressure adjustor in the external aqueous phase is about 0.05 to about 30% (w/w).

11. A process according to claim 10 wherein the concentration of the osmotic pressure adjustor in the external aqueous phase is about 1% (w/w).

12. A process according to claim 2, wherein the weight-average molecular weight of the polymer is about 2,000 to about 800,000 daltons as determined by gel permeation chromatography.

13. A process according to claim 2 wherein the polymer is a biodegradable polymer.

14. A process according to claim 13 wherein the biodegradable polymer is a polymer or a copolymer of hydroxycarboxylic acids, or mixtures thereof.

15. A process according to claim 2 wherein the polymer is lactic acid/glycollic acid copolymer.

16. A process according to claim 1, wherein the osmotic pressure adjustor is one or more water-soluble polyhydric alcohol and derivatives thereof.

17. A process according to claim 1, wherein the osmotic pressure adjustor is one or more water-soluble monohydric alcohol and derivatives thereof.

18. A process according to claim 1, wherein the osmotic pressure adjustor is one or more water-soluble monosaccharide and derivatives thereof.

19. A process according to claim 1, wherein the osmotic pressure adjustor is one or more water-soluble disaccharide and derivatives thereof.

20. A process according to claim 1, wherein the osmotic pressure adjustor is one or more water-soluble oligosaccharide and derivatives thereof.

21. A process according to claim 1, wherein the osmotic pressure adjustor is one or more water-soluble amino acid and salts thereof.