Preparation and in Vitro Evaluation of Polylactic Acid (PLA) or Polylactic-co-Glycolic Acid (PLGA) Microcapsules Loaded with Estradiol

摘要

Aim PLA/PLGA was used as biodegradable and biocompatible carriers to achieve sustained release of es-tradiol (E_2). Methods Microcapsules (MC) were prepared by an emulsification-solvent extraction method, and then the properties and in vitro drug release behavior of MC were examined. An analysis of variance (ANOVA) was used to test the statistical significance. Then, multiple comparisons were made with a T-method between levels to examine the significance of difference further. For all the results a P value >0.05 was considered statistically insignificant . Results Under the same conditions, the water-adding speed and the particle size had significant effects (P < 0.01) on the entrapment efficiency of MC; the water-adding speed and the concentration of PLA in the oil phase had significant effects ( P < 0.01) on the diameter MC in medium. Release of E_2 from MC was influenced significantly (P < 0.01) by the water-adding speed and the type and molecule weight of the polymers. But the differences between levels of the variates were not all significant. Conclusion E_2 -PLA/PLGA-MC with various properties can be formed when the formulation and the technology were changed accordingly.