dc.creatorMoreno, María Alejandra
dc.creatorGómez Mascaraque, Laura Gómez
dc.creatorArias, Myriam Elizabeth
dc.creatorZampini, Iris Catiana
dc.creatorSayago, Jorge Esteban
dc.creatorRamos, Liudis Leidy Pino
dc.creatorSchmeda Hirschmann, Guillermo
dc.creatorLopez Rubio, Amparo
dc.creatorIsla, Maria Ines
dc.date.accessioned2020-04-06T18:33:19Z
dc.date.accessioned2022-10-14T21:32:43Z
dc.date.available2020-04-06T18:33:19Z
dc.date.available2022-10-14T21:32:43Z
dc.date.created2020-04-06T18:33:19Z
dc.date.issued2018-12
dc.identifierMoreno, María Alejandra; Gómez Mascaraque, Laura Gómez; Arias, Myriam Elizabeth; Zampini, Iris Catiana; Sayago, Jorge Esteban; et al.; Electrosprayed Chitosan Microcapsules as Delivery Vehicles for Vaginal Phytoformulations; Elsevier; Carbohydrate Polymers; 201; 12-2018; 425-437
dc.identifier0144-8617
dc.identifierhttp://hdl.handle.net/11336/102061
dc.identifierCONICET Digital
dc.identifierCONICET
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/4309060
dc.description.abstractThe design of novel delivery systems to treat vaginal fungalinfections is a topic of high interest. Chitosan, being itselfantimicrobial and having good mucoadhesive properties, is an excellentcandidate as a delivery matrix for active compounds. In this work,chitosan microcapsules containing dry extracts of Argentinean medicinalplants with proved biological properties (Larrea divaricata, L.cuneifolia, L. nitida, Zuccagnia punctata and Tetraglochin andina) weredeveloped through electrospraying and compared with conventionally usedtablets containing the same extracts. Total phenolics(spectrophotometry), morphology and particle size (SEM), molecularorganization (FT-IR spectroscopy), water sorption capacity, release ofbioactive compounds (BC) and biological properties were assessed. Theencapsulation process did not degrade the BC, as antioxidant andantifungal capacity remained unchanged. The FT-IR analysis suggestedinteractions via hydrogen bonding or hydrophobic interactions between thechitosan and the extracts, which explained why the microcapsules kept theintegrity in slightly acidic media. Increased solubility of the extractswhen incorporated in the microcapsules was seen in simulated vaginalfluid, potentially increasing the bioavailability of BC in the vaginalenvironment. This work highlights the potential of the chitosan-baseddelivery systems for phytomedicines with antifungal and antioxidantactivity to be used in vulvovaginal candidiasis.
dc.languageeng
dc.publisherElsevier
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1016/j.carbpol.2018.08.084
dc.relationinfo:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S0144861718309925
dc.rightshttps://creativecommons.org/licenses/by-nc-nd/2.5/ar/
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectANTI-CANDIDA
dc.subjectARGENTINEAN DRY PLANT EXTRACTS
dc.subjectMICROCAPSULES
dc.subjectVAGINAL TABLETS
dc.titleElectrosprayed Chitosan Microcapsules as Delivery Vehicles for Vaginal Phytoformulations
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:ar-repo/semantics/artículo
dc.typeinfo:eu-repo/semantics/publishedVersion


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