How porosity and size affect the drug release mechanisms from PLGA-based microparticles
- 28 February 2006
- journal article
- research article
- Published by Elsevier in International Journal of Pharmaceutics
- Vol. 314 (2) , 198-206
- https://doi.org/10.1016/j.ijpharm.2005.07.031
Abstract
No abstract availableKeywords
This publication has 18 references indexed in Scilit:
- How Autocatalysis Accelerates Drug Release from PLGA-Based Microparticles: A Quantitative TreatmentBiomacromolecules, 2005
- Mapping neutral microclimate pH in PLGA microspheresJournal of Controlled Release, 2005
- Modeling small-molecule release from PLG microspheres: effects of polymer degradation and nonuniform drug distributionPublished by Elsevier ,2004
- Size and temperature effects on poly(lactic-co-glycolic acid) degradation and microreservoir device performanceBiomaterials, 2004
- Biocompatibility of implantable synthetic polymeric drug carriers: focus on brain biocompatibilityBiomaterials, 2003
- A New Mathematical Model Quantifying Drug Release from Bioerodible Microparticles Using Monte Carlo SimulationsPharmaceutical Research, 2002
- Polymer and microsphere blending to alter the release of a peptide from PLGA microspheresEuropean Journal of Pharmaceutics and Biopharmaceutics, 2000
- Influence of particle size and dissolution conditions on the degradation properties of polylactide-co-glycolide particlesBiomaterials, 2000
- Hydrolytic degradation of devices based on poly(dl-lactic acid) size-dependencePublished by Elsevier ,1999
- Poly(lactide-co-glycolide) decomposition kinetics in vivo and in vitroMacromolecules, 1987