INVESTIGADORES
ESTENOZ Diana Alejandra
congresos y reuniones científicas
Título:
Analysis of Particle Size, Polydispersity and Polymer Degradation on Progesterone Delivery from PLGA-Based Microparticles: Experimental and Mathematical Modeling
Autor/es:
BUSATTO, CARLOS; PESOA, JUAN; IGNACIO HEBLING; JULIO LUNA; DIANA ESTENOZ
Reunión:
Simposio; 18th International Biotechnology Symposium and Exhibition; 2018
Resumen:
Poly(lactic-co-glycolic acid) (PLGA) has been widely studied as biomaterial for drug delivery applications. Progesterone is a lipophilic steroid hormone with low molecular weight. Several progesterone delivery systems based on biodegradable and non-biodegradable polymeric matrices has been used for estrousregulation in production animals. Biodegradable microparticles are of special interest because they present several advantages, such as easy preparation and administration, do not require surgical intervention to remove the material and it is possible to control the release and degradation rates based onthe physicochemical properties of the polymer. In this study, PLGA microparticles for progesterone delivery were prepared by the solvent extraction/evaporation and microfluidic techniques. Microparticles werecharacterized by size distribution, morphology, encapsulation efficiency and thermal properties. The effect of particle size, polydispersity and polymer degradation on the in vitro release of progesterone was studied.Biphasic and triphasic release profiles were observed for smaller and larger microparticles, respectively. This behavior is related to the complete drug release in a few days for smaller microparticles, during whichpolymer degradation effects are still negligible. Microparticles prepared by microfluidics showed a release profile with high reproducibility compared to microparticles prepared by the conventional technique. Amathematical model for the prediction of progesterone release from PLGA microspheres was developed. Our previous model for the heterogeneous hydrolytic degradation of PLGA microspheres was extended in order to incorporate the drug dissolution and diffusion in the polymeric matrix. The model was adjustedand validated with the experimental data. Simulation results are in very good agreement with experimental results.