Introduction
An in vitro dissolution model has been developed to describe the drug release from orntide-loaded PLGA microspheres. Literature data for the degradation rates of various PLGA polymers obtained from literature were used to parameterize the in vitro dissolution
model to predict the differences in drug release from PLGA microspheres with varying lactic acid/glycolic acid (LA/GA) ratios. We then assessed the ability of the model to predict new formulations with different LA/GA ratios using published data for orntide-loaded PLGA microspheres.
Controlled Release Society Annual Meeting & Exposition, July 16-19, 2017, Boston, MA
By James Mullin, William van Osdol, Viera Lukacova, Walter S. Woltosz, Michael B. Bolger