Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/106193
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dc.contributor.authorSouto, Eliana B.-
dc.contributor.authorZielińska, Aleksandra-
dc.contributor.authorSouto, Selma B-
dc.contributor.authorDurazzo, Alessandra-
dc.contributor.authorLucarini, Massimo-
dc.contributor.authorSantini, Antonello-
dc.contributor.authorAtanasov, Atanas G.-
dc.contributor.authorMarques, Conrado-
dc.contributor.authorAndrade, Luciana N.-
dc.contributor.authorSeverino, Patrícia-
dc.date.accessioned2023-03-24T09:48:17Z-
dc.date.available2023-03-24T09:48:17Z-
dc.date.issued2020-02-20-
dc.identifier.issn1422-0067pt
dc.identifier.urihttps://hdl.handle.net/10316/106193-
dc.description.abstractIn this work, we developed a solid lipid nanoparticle (SLN) formulation with (+)-limonene 1,2-epoxide and glycerol monostearate (Lim-SLNs), stabilized with Poloxamer® 188 in aqueous dispersion to modify the release profile of the loaded monoterpene derivative. We also evaluated the role of SLNs in lipid peroxidation and cytotoxicity in a spontaneously transformed aneuploid immortal keratinocyte cell line from adult human skin (the HaCaT cell line). For the cell viability assay, the colorimetric 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2H-tetrazolium bromide (MTT) assay was used. Lim-SLNs with a loading capacity and encapsulation efficiency of 0.39% and 63%, respectively, were produced by high pressure homogenization. A mean particle size of 194 ± 3.4 nm and polydispersity index of 0.244 were recorded for the loaded Lim-SLNs, as compared to 203 ± 1.5 nm (PI 0.213) for the non-loaded (blank) SLNs. The loading of the monoterpene derivative into glycerol monostearate SLNs fitted into the zero-order kinetics, and ameliorated both lipid peroxidation and cytotoxicity in a keratinocyte cell line. A promising formulation for antioxidant and anti-tumoral activities is here proposed.pt
dc.language.isoengpt
dc.publisherMDPIpt
dc.relationCNPq (Conselho Nacional de Desenvolvimento Científico e Tecnológicopt
dc.relationCAPES (Coordenação de Aperfeiçoamento de Pessoal de Nível Superior)pt
dc.relationFAPITEC/SE (Fundação de Apoio à Pesquisa e Inovação Tecnológica do Estado de Sergipe)pt
dc.relationM-ERA-NET-0004/2015-PAIREDpt
dc.relationUIDB/04469/2020pt
dc.relationPEst-OE/UID/AGR/04033/2019pt
dc.rightsopenAccesspt
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt
dc.subject(+)-limonene 1pt
dc.subject2-epoxidept
dc.subjectmonoterpenept
dc.subjectImwitor 900K-SLNpt
dc.subjectlipid peroxidationpt
dc.subjectcytotoxicitypt
dc.subjectHaCaT cell linept
dc.subject.meshCell Linept
dc.subject.meshDelayed-Action Preparationspt
dc.subject.meshHumanspt
dc.subject.meshKeratinocytespt
dc.subject.meshLipid Peroxidationpt
dc.subject.meshNanoparticlespt
dc.subject.meshAntioxidantspt
dc.subject.meshCyclohexane Monoterpenespt
dc.subject.meshMonoglyceridespt
dc.subject.meshPoloxamerpt
dc.title(+)-Limonene 1,2-Epoxide-Loaded SLNs: Evaluation of Drug Release, Antioxidant Activity, and Cytotoxicity in an HaCaT Cell Linept
dc.typearticle-
degois.publication.firstPage1449pt
degois.publication.issue4pt
degois.publication.titleInternational Journal of Molecular Sciencespt
dc.peerreviewedyespt
dc.identifier.doi10.3390/ijms21041449pt
degois.publication.volume21pt
dc.date.embargo2020-02-20*
uc.date.periodoEmbargo0pt
item.cerifentitytypePublications-
item.languageiso639-1en-
item.fulltextCom Texto completo-
item.grantfulltextopen-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypearticle-
crisitem.author.orcid0000-0002-9737-6017-
crisitem.author.orcid0000-0003-2603-1377-
crisitem.author.orcid0000-0001-6527-6612-
Appears in Collections:FFUC- Artigos em Revistas Internacionais
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