Abstract

The current work aimed to fabricate a rice bran phospholipid-based nanovesicular system for oral and topical delivery of capsaicinoids from Capsicum annuum. Using a modified thin film-hydration method, capsaicinoid-loaded nanovesicles (CLNVs) with encapsulation efficiency of 92.31 ± 5.35% and a mean diameter of 134 ± 2 nm, were produced. Based on in vitro release studies, the produced CLNVs exhibited a slow and limited release in both simulated salivary and gastric fluids, and selective release in simulated intestinal fluid, suggesting the opportunity for targeting release via the gastro-intestinal tract during oral delivery. Furthermore, the observed limited release of capsaicinoids in surfactant solution is a desirable property for topical delivery formulations. The fabricated delivery vehicle has also shown a masked and reduced irritation effect that co-occur with the strong anti-inflammatory activity of the capsaicinoids. Using a modified duck egg chorioallantoic membrane (CAM) assays, it was demonstrated that encapsulation into nanovesicles was able to reduce the irritancy of capsaicinoids by almost 50% and, at the same time, improve the anti-inflammatory activity by up to 10 folds. These results demonstrated the potential of CLNVs to be developed as oral and topical delivery systems for capsaicinoids.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.