Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
601677 | Colloids and Surfaces B: Biointerfaces | 2010 | 8 Pages |
Abstract
Particles for subcutaneous depot use encapsulating a model water-soluble drug have been produced from poly(lactic–glycolic acid) (PLGA) using a membrane emulsification—solvent evaporation technique. The release behaviour, mainly the change in size and inner morphology are reported. During release, the particles initially swelled in size, then reduced. A diffusion based model, taking in to account the change in particle size, is presented. Surface erosion is evident from the particle size and image evidence, and the diffusion model provides a fit to the data even during the surface erosion period, suggesting that the model drug diffuses before the particle degrades.
Related Topics
Physical Sciences and Engineering
Chemical Engineering
Colloid and Surface Chemistry
Authors
G. Gasparini, R.G. Holdich, S.R. Kosvintsev,