Drug Release from Nanoparticles of Poly(DL-lactide-co-glycolide)

Korean Journal of Chemical Engineering

Volumn 17, Issue 2, 2000, Pages 230-236

  Nah, Jae Woon ^a   Jeong, Young Il ^b   Koh, Jae Joon ^c  

^a Sunchon National University   (South Korea)

^b KYOTO PHARMACEUTICAL UNIVERSITY   (Japan)

^c Seoul National University   (South Korea)

Author keywords

Clonazepam; Controlled Drug Release; Dialysis Method; Nanoparticles; Poly(DL lactide co glycolide)

Indexed keywords

EID: 0034402954     PISSN: 02561115     EISSN: None     Source Type: Journal    
DOI: 10.1007/BF02707148     Document Type: Article

References (34)

1. Alleman, E., Gurny, R. and Doelker, E., "Drug-Loaded Nanoparticles-Preparation Methods and Drug Targeting Issues," Eur. J. Pharm. Biopharm., 39, 173 (1993).
2. Cho, C. S., Na, J. W., Jeong, Y. I., Kim, S. H., Lee, Y. M. and Sung, Y. M., "Micelle Formation of the Hexablock Copolymer Consisting of Poly(γ-benzyl L-glutamate) as the Hydrophobic Part and Poly(ethylene oxide) as the Hydrophilic Part," Polymer (Korea), 19, 926 (1995).
3. Ciftci, K., Suheyla Kas, H., Atilla Hincal, A., Meral Ercan, T., Guven, O. and Ruacan, S., "In Vitro and In Vivo Evaluation of PLGA (50/50) Microspheres Containing 5-Fluorouracil Prepared by a Solvent Evaporation Method," Int. J. Pharm., 131, 73 (1996).
4. Couvreur, P., Fattal, E. and Andremont, A., "Liposomes and Nanoparticles in the Treatment of Intracellular Bacterial Infections," Pharm. Res., 8, 1079 (1991).
5. Couvreur, P., Fattal, E., Alphandary, H., Puisieux, F. and Andremont, A., "Intracellular Targeting of Antibiotics by Means of Biodegradable Nanoparticles," J. Control. Release, 19, 259 (1992).
6. Davis, S. S., "Colloids as Drug-Delivery Systems," Pharmaceut. Technol., 5, 71 (1981).
7. Kreuter, J., "Nanoparticle-Based Drug Delivery Systems," J. Control. Release, 16, 169 (1991).
8. Davis, S. S., Illum, L., Moghimi, S. M., Davies, M. C., Porter, C. J. H., Muir, I. S., Brindley, A., Christy, N. M., Norman, M. E., Williams, P. and Dunn, S. E., "Microspheres for Targeting Drugs to Specific Body Sites," J. Control. Release, 24, 157 (1993).
9. Dunn, S. E., Brindley, A., Davis, S. S., Davies, M. C. and Illum, L., "Polystyrene-Poly(ethylene glycol) (PS-PEG 2000) Particles as Model Systems for Site Specific Drug Delivery. 2. The Effect of PEG Surface Density on the In Vitro Cell Characterization and In Vivo Biodistribution," Pharm. Res., 11, 1016 (1994).
10. Govender, T., Stolnik, S., Garnett, M. C., Illum, L. and Davis, S. S., "PLGA Nanoparticles Prepared by Nanoprecipitation: Drug Loading and Release Studies of a Water Soluble Drug," J. Control. Release, 57, 171 (1999).
11. Gref, R., Minamitake, Y., Peracchia, M. T., Trubetskoy, V., Torchilin, V. and Langer, R., "Biodegradable Long-Circulating Polymeric Nanospheres," Science, 263, 1600 (1994).
12. Illum, L., Davis, S. S., Wilson, C. G., Frier, M., Hardy, J. G. and Thomas, N. W., "Blood Clearance and Organ Deposition of Intravenously Administered Colloidal Particles: The Effects of Particle Size, Nature and Shape," Int. J. Pharm., 12, 135 (1982).
13. Illum, L., Hunneyball, I. M. and Davis, S. S., "The Effect of Hydrophilic Coatings on the Uptake of Colloidal Particles by the Liver and by Peritoneal Macrophages," Int. J. Pharm., 29, 53 (1986).
14. Jeffery, H., Davis, S. S. and O'Hagan, D. T., "The Preparation and Characterization of Poly(lactide-co-glycolide) Microparticles. I. Oil-in Water Emulsion Solvent Evaporation," Int. J. Pharm., 77, 169 (1991).
15. Jeong, Y. I., Cheon, J. B., Kim, S. H., Nah, J. W., Lee, Y. M., Sung, Y. K., Akaike, T. and Cho, C. S., "Clonazepam Release from Core-Shell Type Nanoparticles in vitro," J. Control. Release, 51, 169 (1998).
16. Juliene, M. C., Alonso, M. J., Gomez Amoza, J. L. and Benoit, J. P., "Preparation of Poly(dl-lactide/glycolide) Nanoparticles of Controlled Particle Size Distribution: Application of Experimental Design," Drug Dev. Ind. Pharm., 18, 1063 (1992).
17. Kwon, G. S., Naito, M., Yokoyama, M., Okano, T., Sakurai, Y. and Kataoka, K., "Physical Entrapment of Adriamycin in AB Block Copolymer Micelles," Pharm. Res., 12, 192 (1995).
18. Lasic, D. D., "Mixed Micelles in Drug Delivery," Nature, 355, 279 (1992).
19. Leroux, J. C., Allemann, E., Jaeghere, F. D., Doelker, E. and Gurny, R., "Biodegradable Nanoparticles-From Sustained Release Formulations to Improved Site Specific Drug Delivery," J. Control. Release, 39, 339 (1996).
20. Muller, R. H., Wallis, K. H., Troster, S. D. and Kreuter, J., "In Vitro Characterization of Poly(methyl-methacrylate) Nanoparticles and Correlation to their In Vivo Fate," J. Control. Release, 20, 237 (1992).
21. Mura, P., Liguori, A., Bramanti, G., Corti, P., Murratzu, C. and Celesti, L., "In Vitro Study of Clonazepam Diffusion Kinetics from Solutions or Hydrophilic Gel," Pharm. Acta Helv., 65, 298 (1990).
22. Nah, J. W., Jeong, Y. I. and Cho, C. S., "Clonazepam Release from Core-Shell Type Nanoparticles Composed of Poly(γ-benzyl L-glutamate) as the Hydrophobic Part and Poly(ethylene oxide) as the Hydrophilic Part," J. Polym. Sci., Polym. Phys., 36, 415 (1998).
23. Peracchia, M. T., Gref, R., Minamitake, Y., Domb, A., Lotan, N. and Langer, R., "PEG-Coated Nanospheres from Amphiphilic Diblock and Multiblock Copolymers: Investigation of their Drug Encapsulation and Release Characteristics," J. Control. Release, 46, 223 (1997).
24. Scholes, P. D., Coombes, A. G. A., Illum, L., Davis, S. S., Vert, M. and Davies, M. C., "The Preparation of Sub-200 nm Poly(lactide-co-glycolide) Microspheres for Site-Specific Drug Delivery," Control. Release, 25, 145 (1993).
25. Seijo, B., Fattal, E., Roblot-Treupel, L. and Couvreur, P., "Design of Nanoparticles of Less than 50 nm Diameter Preparation, Characterization and Drug Loading," Int. J. Pharm., 62, 1 (1990).
26. Shin, I. G., Kim, S. Y., Lee, Y. M., Cho, C. S. and Sung, Y. K., "Methoxy Poly(ethylene glycol)/-Caprolactone Amphiphilic Block Copolymeric Micelle Containing Indomethacin. I. Preparation and Characterization," J. Control. Release, 51, 1 (1998).
27. Sjostrom, B., Bergenstahl, B. and Kronberg, B., "A Method for the Preparation of Submicron Particles of Sparingly Water-Soluble Drugs by Precipitationin Oil-in Water Emulsions. II: Influence of the Emulsifier, the Solvent, and the Drug Substance," J. Pharm. Sci., 82, 585 (1993b).
28. Sjostrom, B., Kaplun, A., Talmon, Y. and Cabane, B., "Structure of Nanoparticles Prepared from Oil-in Water Emulsions," Pharm. Res., 12, 39 (1995).
29. Sjostrom, B., Kronberg, Br. and Carlfors, J., "A Method for the Preparation of Submicron Particles of Sparingly Water-Soluble Drugs by Precifitation in Oil-in Water Emulsions, I. Influence of Emulsification and Surfactant Concentration," J. Pharm. Sci., 82, 579 (1993a).
30. White, H. S., ,"Antiepileptic Drugs," In The Science and Practice of Pharmacy, Remington, Vol. 2, 19th ed.; A. R. Gennaro, Eds.; Mack Publishing Co.: Easton, Pennsylvania, USA, 1173 (1995).
31. Venier-Julienne, M. C. and Benoit, J. P., "Preparation, Purification and Morphology of Polymeric Nanoparticles as Drug Carriers," Pharm. Acta Helv., 71, 121 (1996).
32. Witschi, C. and Doelker, E., "Residual Solvents in Pharmaceutical Products: Acceptable Limits, Influences on Physicochemical Properties, Analytical Methods and Documented Values," Eur. J. Pharm. Biopharm., 43, 215 (1997).
33. Yoshioka, T., Hashida, M., Muranishi, S. and Sezaki, H., "Specific Delivery of Mitomycin C to the Liver, Spleen and Lung: Nano- and Microspherical Carriers of Gelatin," Int. J. Pharm., 81, 131 (1981).
34. Zhang, X., Jackson, J. K. and Burt, H. M., "Development of Amphiphilic Diblock Copolymers as Micellar Carriers of Taxol," Int. J. Pharm., 132, 195 (1996).