dc.contributorUniversidade Estadual Paulista (UNESP)
dc.creatorChiari, Bruna Galdorfini
dc.creatorMartini, Paula Cressoni
dc.creatorMoraes, Jemima Daniela Dias
dc.creatorAndréo, Rogério
dc.creatorCorrea, Marcos Antonio
dc.creatorCicarelli, Regina Maria Barretto
dc.creatorIsaac, Vera Lucia Borges
dc.date2015-05-15T13:30:32Z
dc.date2016-10-25T20:48:53Z
dc.date2015-05-15T13:30:32Z
dc.date2016-10-25T20:48:53Z
dc.date2012
dc.date.accessioned2017-04-06T08:17:53Z
dc.date.available2017-04-06T08:17:53Z
dc.identifierInternational Journal of Research in Cosmetic Science, v. 2, n. 2, p. 8-14, 2012.
dc.identifier2277-7172
dc.identifierhttp://hdl.handle.net/11449/123632
dc.identifierhttp://acervodigital.unesp.br/handle/11449/123632
dc.identifier9703848266137282
dc.identifier6153974945085893
dc.identifier4457249333748704
dc.identifier4842462513285606
dc.identifierhttp://www.upjournals.com
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/934242
dc.descriptionThe importance of this study is based on the need to obtain simple and efficient in vitro models to predict the in vivo toxicity of cosmetics, aiming not to use animals as experimental model. Here, we proposed the use of HepG2 cells, which are widely applied to simulate the hepatic function of the human organism in vitro. This cell line was chose since recent studies have shown that the liver is potentially the most frequently targeted organ by cosmetic ingredients, and beyond that, considering the widely application of in vitro assays to test the cutaneous permeation of cosmetic products, including the assays applying modified Franz cells, this technique becomes indispensable. Three different cosmetic active substances were used, and the toxicity to HepG2 cells was assessed by the MTT method. The treatment with hyaluronic acid showed no toxicity to HepG2 cells. Treating the cells with P. guajava L. extract were verified that increasing the amount of the extract in the media, the cellular viability decreased, and finally, the treatment of alpha-lipoic acid showed a cytoprotective effect in relation to the treatment with propylene glycol. The study demonstrated the suitability in using HepG2 cells to assess the safety of cosmetic active substances, helping in the prediction of if the substance could be hepatotoxic if could reach the bloodstream
dc.languageeng
dc.relationInternational Journal of Research in Cosmetic Science
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectHepG2
dc.subjectcitotoxicity
dc.titleUse of HEPG2 cells to assay the safety of cosmetic active substances
dc.typeOtro


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