dc.creator | Guzman Oyarzo, Dina | |
dc.creator | Plaza, Tanya | |
dc.creator | Recio Sánchez, Gonzalo | |
dc.creator | Abdalla, Dulcineia S. P. | |
dc.creator | Salazar, Luis A. | |
dc.creator | Hernandez Montelongo, Jacobo | |
dc.date | 2019 | |
dc.date | 2021-04-30T16:46:58Z | |
dc.date | 2021-04-30T16:46:58Z | |
dc.date.accessioned | 2021-06-14T22:08:42Z | |
dc.date.available | 2021-06-14T22:08:42Z | |
dc.identifier | PHARMACEUTICS,Vol.11,,2019 | |
dc.identifier | http://repositoriodigital.uct.cl/handle/10925/3439 | |
dc.identifier | 10.3390/pharmaceutics11060289 | |
dc.identifier.uri | http://repositorioslatinoamericanos.uchile.cl/handle/2250/3301528 | |
dc.description | Propolis is widely recognized for its various therapeutic properties. These are attributed to its rich composition in polyphenols, which exhibit multiple biological properties (e.g., antioxidant, anti-inflammatory, anti-angiogenic). Despite its multiple benefits, oral administration of polyphenols results in low bioavailability at the action site. An alternative to face this problem is the use of biomaterials at nano-micro scale due to its high versatility as carriers and delivery systems of various drugs and biomolecules. The aim of this work is to determine if nPSi-beta CD microparticles are a suitable material for the load and controlled release of caffeic acid (CA) and pinocembrin (Pin), two of the main components of a Chilean propolis with anti-atherogenic and anti-angiogenic activity. Polyphenols and nPSi-beta CD microparticles cytocompatibility studies were carried out with human umbilical vein endothelial cells (HUVECs). Results from physicochemical characterization demonstrated nPSi-beta CD microparticles successfully retained and controlled release CA and Pin. Furthermore, nPSi-beta CD microparticles presented cytocompatibility with HUVECs culture at concentrations of 0.25 mg/mL. These results suggest that nPSi-beta CD microparticles could safely be used as an alternate oral delivery system to improve controlled release and bioavailability of CA or Pin-and eventually other polyphenols-thus enhancing its therapeutic effect for the treatment of different diseases. | |
dc.language | en | |
dc.publisher | MDPI | |
dc.source | PHARMACEUTICS | |
dc.subject | controlled release | |
dc.subject | nanoporous silicon | |
dc.subject | beta CD polymer | |
dc.subject | caffeic acid | |
dc.subject | pinocembrin | |
dc.subject | polyphenols | |
dc.subject | HUVECs | |
dc.title | Use of nPSi-beta CD Composite Microparticles for the Controlled Release of Caffeic Acid and Pinocembrin, Two Main Polyphenolic Compounds Found in a Chilean Propolis | |
dc.type | Article | |