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Solid lipid nanoparticles optimized by 22 factorial design for skin administration: Cytotoxicity in NIH3T3 fibroblasts

dc.contributor.authorRigon, Roberta Balansin [UNESP]
dc.contributor.authorGonçalez, Maíra Lima [UNESP]
dc.contributor.authorSeverino, Patrícia
dc.contributor.authorAlves, Danilo Antonini
dc.contributor.authorSantana, Maria H.A.
dc.contributor.authorSouto, Eliana B.
dc.contributor.authorChorilli, Marlus [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionTiradentes University
dc.contributor.institutionUniversidade Estadual de Campinas (UNICAMP)
dc.contributor.institutionUniversity of Coimbra (FFUC)
dc.contributor.institutionUniversity of Coimbra
dc.date.accessioned2018-12-11T17:21:58Z
dc.date.available2018-12-11T17:21:58Z
dc.date.issued2018-11-01
dc.description.abstractThe present study focuses on the characterization of the cytotoxic profile on NIH3T3 mouse embryonic fibroblasts of solid lipid nanoparticles (SLN) optimized by a 22 full factorial design for skin administration. To build up the surface response charts, a design of experiments (DoE) based on 2 independent variables was used to obtain an optimized formulation. The effect of the composition of lipid and water phases on the mean particle size (z-AVE), polydispersity index (PdI) and zeta potential (ZP) was studied. The developed formulations were composed of 5.0% of lipid phase (stearic acid (SA), behenic alcohol (BA) or a blend of SA:BA (1:1)) and 4.7% of surfactants (soybean phosphatidylcholine and poloxamer 407). In vitro cytotoxicity using NIH3T3 fibroblasts was performed by MTT reduction assay. This factorial design study has proven to be a useful tool in optimizing SLN (z-AVE ∼ 200 nm), which were shown to be non-cytotoxic. The present results highlight the benefit of applying statistical designs in the preparation and optimization of SLN formulations.en
dc.description.affiliationFaculty of Pharmaceutical Sciences UNESP – São Paulo State University Departamento de Fármacos e Medicamentos, Campus Araraquara
dc.description.affiliationCentre of Biological Sciences and Health Tiradentes University
dc.description.affiliationLaboratory of Biotechnology Institute of Biology Campinas University (UNICAMP), Campinas
dc.description.affiliationFaculty of Chemical Engineering Campinas University (UNICAMP), Campinas
dc.description.affiliationDepartment of Pharmaceutical Technology Faculty of Pharmacy University of Coimbra (FFUC), Polo das Ciências da Saúde Azinhaga de Santa Comba
dc.description.affiliationREQUIMTE/LAQV Group of Pharmaceutical Technology Faculty of Pharmacy University of Coimbra
dc.description.affiliationUnespFaculty of Pharmaceutical Sciences UNESP – São Paulo State University Departamento de Fármacos e Medicamentos, Campus Araraquara
dc.format.extent501-505
dc.identifierhttp://dx.doi.org/10.1016/j.colsurfb.2018.07.065
dc.identifier.citationColloids and Surfaces B: Biointerfaces, v. 171, p. 501-505.
dc.identifier.doi10.1016/j.colsurfb.2018.07.065
dc.identifier.file2-s2.0-85050850577.pdf
dc.identifier.issn1873-4367
dc.identifier.issn0927-7765
dc.identifier.lattes1427125996716282
dc.identifier.scopus2-s2.0-85050850577
dc.identifier.urihttp://hdl.handle.net/11449/176661
dc.language.isoeng
dc.relation.ispartofColloids and Surfaces B: Biointerfaces
dc.relation.ispartofsjr1,071
dc.rights.accessRightsAcesso abertopt
dc.sourceScopus
dc.subjectFactorial design
dc.subjectFibroblasts
dc.subjectMTT assay
dc.subjectSkin administration
dc.subjectSolid lipid nanoparticles
dc.titleSolid lipid nanoparticles optimized by 22 factorial design for skin administration: Cytotoxicity in NIH3T3 fibroblastsen
dc.typeArtigopt
dspace.entity.typePublication
relation.isDepartmentOfPublicatione214da1b-9929-4ae9-b8fd-655e9bfeda4b
relation.isDepartmentOfPublication.latestForDiscoverye214da1b-9929-4ae9-b8fd-655e9bfeda4b
unesp.author.lattes1427125996716282
unesp.author.orcid0000-0002-9737-6017 0000-0002-9737-6017[6]
unesp.departmentFármacos e Medicamentos - FCFpt

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