Principles of encapsulating hydrophobic drugs in PLA/PLGA microparticles.

By C. Wischke, S. Schwendeman. International journal of pharmaceutics, 2008

794 citations recorded by the source corpus.

Subfields: Pharmaceutical Science, Pulmonary and Respiratory Medicine

View Paper: https://www.semanticscholar.org/paper/fd463ec202925cede2df2b6b88936f73e607ac14

How researchers see this paper

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In Pharmaceutical Science

1. M. Reslow
2. S. Fredenberg
3. K. Mäder
4. M. Wahlgren
5. Sabine Kempe
6. A. Axelsson

Citations in the corpus

• The mechanisms of drug release in poly(lactic-co-glycolic acid)-based drug delivery systems--a review. (2011, background): “This review focuses on the mechanisms of drug release from PLGA-based DDSs, and is complementary to previous reviews that have emphasized which factors that effect drug release from mainly poly(lactic acid) (PLA)-based DDSs (Alexis, 2005), the encapsulation and release of hydrophobic drugs (Wiscke a”
• In situ forming implants - an attractive formulation principle for parenteral depot formulations. (2012, background): “Supercritical techniques will certainly become more important within the next years [10].”
• Microencapsulation of essential oils with biodegradable polymeric carriers for cosmetic applications (2014, background): “8 interactions between polymer and active agent will affect the diffusion rate across the polymeric matrix, and therefore, the oil release [68].”