Please use this identifier to cite or link to this item: https://hdl.handle.net/11000/5258
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dc.contributor.authorMartínez Ortega, Leticia-
dc.contributor.authorMira, Amalia-
dc.contributor.authorFernández Carvajal, Asia-
dc.contributor.authorMateo Martínez, Carmen Reyes-
dc.contributor.authorMallavia Marín, Ricardo-
dc.contributor.authorFalcó Graciá, Juan Alberto-
dc.contributor.otherDepartamentos de la UMH::Agroquímica y Medio Ambientees
dc.date.accessioned2019-09-05T07:10:36Z-
dc.date.available2019-09-05T07:10:36Z-
dc.date.created2018-12-23-
dc.date.issued2019-09-05-
dc.identifier.issn1999-4923-
dc.identifier.urihttp://hdl.handle.net/11000/5258-
dc.description.abstractPsoriasis is a chronic autoimmune systemic disease with an approximate incidence of 2% worldwide; it is commonly characterized by squamous lesions on the skin that present the typical pain, stinging, and bleeding associated with an inflammatory response. In this work, poly(methyl vinyl ether-alt-maleic ethyl monoester) (PMVEMA-ES) nanofibers have been designed as a delivery vehicle for three therapeutic agents with palliative properties for the symptoms of this disease (salicylic acid, methyl salicylate, and capsaicin). For such a task, the production of these nanofibers by means of the electrospinning technique has been optimized. Their morphology and size have been characterized by optical microscopy and scanning electron microscopy (SEM). By selecting the optimal conditions to achieve the smallest and most uniform nanofibers, approximate diameters of up to 800–900 nm were obtained. It was also determined that the therapeutic agents that were used were encapsulated with high efficiency. The analysis of their stability over time by GC-MS showed no significant losses of the encapsulated compounds 15 days after their preparation, except in the case of methyl salicylate. Likewise, it was demonstrated that the therapeutic compounds that were encapsulated conserved, and even improved, their capacity to activate the transient receptor potential cation channel 1 (TRPV1) channel, which has been associated with the formation of psoriatic lesionses
dc.description.sponsorshipThis research was funded by the Spanish Ministerio de Economía y Competitividad grant numbers MAT-2017-86805-R and MAT-2014-53282-R.-
dc.formatapplication/pdfes
dc.format.extent14es
dc.language.isoenges
dc.rightsinfo:eu-repo/semantics/openAccesses
dc.subjectPMVE/MAes
dc.subjectelectrospinninges
dc.subjectnanofiberses
dc.subjectcapsaicines
dc.subjectpsoriasises
dc.subjectTRPV1es
dc.titleDevelopment of A New Delivery System Based on Drug-Loadable Electrospun Nanofibers for Psoriasis Treatmentes
dc.typeinfo:eu-repo/semantics/articlees
dc.identifier.doi10.3390/pharmaceutics11010014-
dc.relation.publisherversionhttp://dx.doi.org/10.3390/pharmaceutics11010014-
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