Abstract
Ethylene—vinyl acetate microspheres were prepared by an emulsion solvent-evaporation method as sustained delivery carriers of progesterone. Physical state of the drug in the microspheres was affected by drug loading level. As thermal analysis and mathematical release models showed, low payloads of the matrix supported the molecularly dispersed drug. Crystalline drug appeared only as the drug loading level increased. The release process of the crystalline drug produced a porosity increase in the polymeric system; thus, the drug could diffuse through pores and channels. Hence, the porosity of the matrix structure was affected by the payload. This hypothesis could justify the increasing goodness-of-fit of the release data to the square-root model as the drug loading level of the microspheres increased