Preparation of Biodegradable Microcapsules with (W/O/W) Emulsion in Solvent Evaporation

Kagaku Kogaku Ronbunshu

Volumn 23, Issue 2, 1997, Pages 259-265

  Kiyoyama, Shiro ^a   Shiomori, Koichiro ^a   Baba, Yoshinari ^a   Kawano, Yoshinobu ^a   Yoshizawa, Hidekazu ^b   Hatate, Yasuo ^b  

^a UNIVERSITY OF MIYAZAKI   (Japan)

^b KAGOSHIMA UNIVERSITY   (Japan)

Author keywords

(W O W) Emulsion; Biodegradable Microcapsule; Biopol; Solvent Evaporation

Indexed keywords

EID: 21744446940     PISSN: 0386216X     EISSN: 13499203     Source Type: Journal    
DOI: 10.1252/kakoronbunshu.23.259     Document Type: Article

References (20)

1. Bodmeier, R. and J. W. McGinity; “The Preparation and Evaluation of Drug-Containing Poly (dl-lactide) Microspheres Formed by the Solvent Evaporation Method,” Pharmaceutical Research, 4, 465-471 (1987)
2. Ijichi, K., S. Kiyoyama, K. Shiomori, Y. Baba, Y. Kawano and Y. Hatate; “Preparation of Cross-Linked Microcapsules with Spherical Pores by in-situ Polymerization in (W/ O/W) Emulsion System,” Kagaku Kogaku Ronbunshu, in press (1996)
3. Ikada, Y.; Seibunkaiseikoubunsi, p. 125-134, Koubunsikan-koukai, Kyoto, Japan (1994)
4. Leelarasamee, N., S. A. Howard and J. K. H. Ma; “Effect of Surface Active Agents on Drug Release from Polylactic Acid-Hydrocortisone Microcapsules,” J. Microencapsulation, 5, 37-46 (1988)
5. Mathiowitz, E., W. M. Saltzman, A. Domb, Ph. Dor and R. Langer; “Polyanhydride Microspheres as Drug Carriers. II. Microencapsulation by Solvent Removal,” J. Appli. Polym. Sci., 35, 755-774 (1988)
6. Maulding, H. V. T. R. Tice, D. R. Cowsar, J. W. Fong, J. E. Peason and J. P. Nazareno; “Biodegradable Microcapsules; Acceleration of Polymeric Excipient Hydrolytic Rate by Incorporation of a Basic Medication,” J. Controlled Release, 3, 103-117 (1986)
7. Nihant, N., C. Schugens, C. Grandfils, R. Jerome,and P. Teyssie,; “Polylactide microparticles prepared by Double Emulsion-Evaporation. II. Effect of the Poly (Lactide-co-Glycolide) Composition on the Stability of the Primary and Secondary Emulsions,” J. Colloid and interface Sci., 173, 55-65 (1995)
8. Ogawa, Y., M. Tamamoto, H. Okada, T. Yashiki and T. Shimamoto; “A New Technique to Efficiently Entrap Leuprolide Acetate into Microcapsules of Polylactic Acid or Copoly (lactic/glycolic) Acid,” Chem. Pharm. Bull., 36, 1095-1103 (1988)
9. Vasscher, G. E., J. E. Peason, J. W. Fong, G. S. Argentieri, R. L. Robinson and H. V. Maulding; “Effect of Particle Size on the in vitro and in vivo Degradation Rates of Poly (DL-lactide-co-glycolide) Microcapsules,” J. Biomed. Mater. Res., 22, 73-746 (1988)
10. Zhou, M. X. and T. M. S. Chang; “Control Release of Prostaglandin E 2 from Polylactic Acid Microcapsules, Microparticles and Modified Microparticles,” J. Microencapsulation, 5, 27-36 (1988)
11. Bodmeier, R. and J. W. McGinity; “The Preparation and Evaluation of Drug-Containing Poly (dl-lactide) Microspheres Formed by the Solvent Evaporation Method,” Pharmaceutical Research, 4, 465-471 (1987)
12. Ijichi, K., S. Kiyoyama, K. Shiomori, Y. Baba, Y. Kawano and Y. Hatate; “Preparation of Cross-Linked Microcapsules with Spherical Pores by in-situ Polymerization in (W/ O/W) Emulsion System,” Kagaku Kogaku Ronbunshu, in press (1996)
13. Ikada, Y.; Seibunkaiseikoubunsi, p. 125-134, Koubunsikan-koukai, Kyoto, Japan (1994)
14. Leelarasamee, N., S. A. Howard and J. K. H. Ma; “Effect of Surface Active Agents on Drug Release from Polylactic Acid-Hydrocortisone Microcapsules,” J. Microencapsulation, 5, 37-46 (1988)
15. Mathiowitz, E., W. M. Saltzman, A. Domb, Ph. Dor and R. Langer; “Polyanhydride Microspheres as Drug Carriers. II. Microencapsulation by Solvent Removal,” J. Appli. Polym. Sci., 35, 755-774 (1988)
16. Maulding, H. V. T. R. Tice, D. R. Cowsar, J. W. Fong, J. E. Peason and J. P. Nazareno; “Biodegradable Microcapsules; Acceleration of Polymeric Excipient Hydrolytic Rate by Incorporation of a Basic Medication,” J. Controlled Release, 3, 103-117 (1986)
17. Nihant, N., C. Schugens, C. Grandfils, R. Jerome,and P. Teyssie,; “Polylactide microparticles prepared by Double Emulsion-Evaporation. II. Effect of the Poly (Lactide-co-Glycolide) Composition on the Stability of the Primary and Secondary Emulsions,” J. Colloid and interface Sci., 173, 55-65 (1995)
18. Ogawa, Y., M. Tamamoto, H. Okada, T. Yashiki and T. Shimamoto; “A New Technique to Efficiently Entrap Leuprolide Acetate into Microcapsules of Polylactic Acid or Copoly (lactic/glycolic) Acid,” Chem. Pharm. Bull., 36, 1095-1103 (1988)
19. Vasscher, G. E., J. E. Peason, J. W. Fong, G. S. Argentieri, R. L. Robinson and H. V. Maulding; “Effect of Particle Size on the in vitro and in vivo Degradation Rates of Poly (DL-lactide-co-glycolide) Microcapsules,” J. Biomed. Mater. Res., 22, 73-746 (1988)
20. Zhou, M. X. and T. M. S. Chang; “Control Release of Prostaglandin E 2 from Polylactic Acid Microcapsules, Microparticles and Modified Microparticles,” J. Microencapsulation, 5, 27-36 (1988)