Abstract
Over the past decades, comprehensive attempts have been made to improve physiological absorption by designing delivery systems, using suitable carriers, and altering the route of administration. Here, the vaginal route was targeted using capsular-shaped biodegradable in situ porous drug-eluting inserts (DEI) using clotrimazole as a model drug and PCL and PEO WSR 303 as rate-controlling polymers. Morphology, thermal properties, and degradation kinetics were assessed in comparison to non-porous DEI. The optimized DEI showed site-specific controlled drug release as per disease need, which may lead to enhanced bioavailability as well as patient compliance with reduced dose-related side effects.
Acknowledgements
The authors are thankful to Ramanbhai Patel College of Pharmacy, Charotar University of Science and Technology for extending their facilities to carry out the research work.
Author contributions
Material preparation, data collection, writing and analysis were performed by the first author. Conceptualization, review, and editing were performed by the corresponding author.
Disclosure statement
The authors declare that there is no conflict of interest with regard to this study.