Methods: The microspheres containing Minocycline were prepared by the w/o/w double emulsion solvent evaporation method. Microsphere formulations were morphologically characterized by scanning electron microscope (SEM). Minocycline loaded PLGA microspheres were subjected to an in vitro release test under static conditions.
Results: The SEM images showed that the size of microspheres containing Minocycline was in the range of 10 microns. The in vitro release experiment showed that the release time was over 26 days. The release profile of Minocycline from PLGA microspheres showed a constant and controlled release. Furthermore, the curve showed that there was a burst release on the eighth day.
Conclusions: In conclusion, the biodegradable PLGA microspheres containing Minocycline were successfully prepared by double emulsion solvent evaporation method. Various factors related to the preparation process influenced the drug encapsulation efficiency and the cumulative drug release was subsequently investigated. Ultimately, spherical PLGA microparticles with encapsulation efficiencies higher than 90% and prolonged Minocycline release over 30 days were obtained.
This abstract is based on research that was funded entirely or partially by an outside source: This work was supported financially by a grant (NO:310-3685) from dental school of Shahid Beheshti university of Medical Sciences, Tehran, Iran