Human skin permeation studies with PPARγ agonist to improve its permeability and efficacy in inflammatory processes

dc.contributor.authorSilva Abreu, Marcelle
dc.contributor.authorEspinoza, Lupe Carolina
dc.contributor.authorRodríguez Lagunas, María José
dc.contributor.authorFábrega Fernández, María José
dc.contributor.authorEspina García, Marta
dc.contributor.authorGarcía López, María Luisa
dc.contributor.authorCalpena Campmany, Ana Cristina
dc.date.accessioned2018-06-12T11:06:46Z
dc.date.available2018-06-12T11:06:46Z
dc.date.issued2017-11-28
dc.date.updated2018-06-12T11:06:46Z
dc.description.abstractRosacea is the most common inflammatory skin disease. It is characterized by erythema, inflammatory papules and pustules, visible blood vessels, and telangiectasia. The current treatment has limitations and unsatisfactory results. Pioglitazone (PGZ) is an agonist of peroxisome proliferator-activated receptors (PPARs), a nuclear receptor that regulates important cellular functions, including inflammatory responses. The purpose of this study was to evaluate the permeation of PGZ with a selection of penetration enhancers and to analyze its effectiveness for treating rosacea. The high-performance liquid chromatography (HPLC) method was validated for the quantitative determination of PGZ. Ex vivo permeation experiments were realized in Franz diffusion cells using human skin, in which PGZ with different penetration enhancers were assayed. The results showed that the limonene was the most effective penetration enhancer that promotes the permeation of PGZ through the skin. The cytotoxicity studies and the Draize test detected cell viability and the absence of skin irritation, respectively. The determination of the skin color using a skin colorimetric probe and the results of histopathological studies confirmed the ability of PGZ-limonene to reduce erythema and vasodilation. This study suggests new pharmacological indications of PGZ and its possible application in the treatment of skin diseases, namely rosacea.
dc.format.extent18 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec674903
dc.identifier.issn1661-6596
dc.identifier.pmid29182532
dc.identifier.urihttps://hdl.handle.net/2445/122906
dc.language.isoeng
dc.publisherMDPI
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.3390/ijms18122548
dc.relation.ispartofInternational Journal of Molecular Sciences, 2017, vol. 18, num. 12
dc.relation.urihttps://doi.org/10.3390/ijms18122548
dc.rightscc-by (c) Silva Abreu, Marcelle et al., 2017
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es
dc.sourceArticles publicats en revistes (Farmàcia, Tecnologia Farmacèutica i Fisicoquímica)
dc.subject.classificationMalalties de la pell
dc.subject.classificationInflamació
dc.subject.otherSkin diseases
dc.subject.otherInflammation
dc.titleHuman skin permeation studies with PPARγ agonist to improve its permeability and efficacy in inflammatory processes
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

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