Modeling small-molecule release from PLG microspheres: effects of polymer degradation and nonuniform drug distribution
- 7 December 2004
- journal article
- Published by Elsevier in Journal of Controlled Release
- Vol. 103 (1), 149-158
- https://doi.org/10.1016/j.jconrel.2004.11.012
Abstract
No abstract availableKeywords
This publication has 19 references indexed in Scilit:
- Etanidazole-loaded microspheres fabricated by spray-drying different poly(lactide/glycolide) polymers: effects on microsphere propertiesJournal of Biomaterials Science, Polymer Edition, 2003
- PLG Microsphere Size Controls Drug Release Rate Through Several Competing FactorsPharmaceutical Research, 2003
- Fabrication of PLG microspheres with precisely controlled and monodisperse size distributionsJournal of Controlled Release, 2001
- Microspheres for protein delivery prepared from amphiphilic multiblock copolymersJournal of Controlled Release, 2000
- Adsorption determines in-vitro protein release rate from biodegradable microspheres: quantitative analysis of surface area during degradationJournal of Controlled Release, 1997
- Effect of Drug Loading and Molecular Weight of Cellulose Acetate Propionate on the Release Characteristics of Theophylline MicrospheresPharmaceutical Research, 1991
- Characteristics of the in vitro release of ibuprofen from polyvinylpyrrolidone solid dispersionsInternational Journal of Pharmaceutics, 1986
- Release of Steroids from a Silicone PolymerJournal of Pharmaceutical Sciences, 1972
- Mechanism of sustained‐action medication. Theoretical analysis of rate of release of solid drugs dispersed in solid matricesJournal of Pharmaceutical Sciences, 1963
- Rate of Release of Medicaments from Ointment Bases Containing Drugs in SuspensionJournal of Pharmaceutical Sciences, 1961