Solid lipid nanoparticles optimized by 22 factorial design for skin administration: Cytotoxicity in NIH3T3 fibroblasts
Autor(a) principal: | |
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Data de Publicação: | 2018 |
Outros Autores: | , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1016/j.colsurfb.2018.07.065 http://hdl.handle.net/11449/176661 |
Resumo: | The 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. |
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Solid lipid nanoparticles optimized by 22 factorial design for skin administration: Cytotoxicity in NIH3T3 fibroblastsFactorial designFibroblastsMTT assaySkin administrationSolid lipid nanoparticlesThe 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.Faculty of Pharmaceutical Sciences UNESP – São Paulo State University Departamento de Fármacos e Medicamentos, Campus AraraquaraCentre of Biological Sciences and Health Tiradentes UniversityLaboratory of Biotechnology Institute of Biology Campinas University (UNICAMP), CampinasFaculty of Chemical Engineering Campinas University (UNICAMP), CampinasDepartment of Pharmaceutical Technology Faculty of Pharmacy University of Coimbra (FFUC), Polo das Ciências da Saúde Azinhaga de Santa CombaREQUIMTE/LAQV Group of Pharmaceutical Technology Faculty of Pharmacy University of CoimbraFaculty of Pharmaceutical Sciences UNESP – São Paulo State University Departamento de Fármacos e Medicamentos, Campus AraraquaraUniversidade Estadual Paulista (Unesp)Tiradentes UniversityUniversidade Estadual de Campinas (UNICAMP)University of Coimbra (FFUC)University of CoimbraRigon, Roberta Balansin [UNESP]Gonçalez, Maíra Lima [UNESP]Severino, PatríciaAlves, Danilo AntoniniSantana, Maria H.A.Souto, Eliana B.Chorilli, Marlus [UNESP]2018-12-11T17:21:58Z2018-12-11T17:21:58Z2018-11-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article501-505application/pdfhttp://dx.doi.org/10.1016/j.colsurfb.2018.07.065Colloids and Surfaces B: Biointerfaces, v. 171, p. 501-505.1873-43670927-7765http://hdl.handle.net/11449/17666110.1016/j.colsurfb.2018.07.0652-s2.0-850508505772-s2.0-85050850577.pdf1427125996716282Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengColloids and Surfaces B: Biointerfaces1,071info:eu-repo/semantics/openAccess2024-06-24T13:46:12Zoai:repositorio.unesp.br:11449/176661Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T21:34:19.906687Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Solid lipid nanoparticles optimized by 22 factorial design for skin administration: Cytotoxicity in NIH3T3 fibroblasts |
title |
Solid lipid nanoparticles optimized by 22 factorial design for skin administration: Cytotoxicity in NIH3T3 fibroblasts |
spellingShingle |
Solid lipid nanoparticles optimized by 22 factorial design for skin administration: Cytotoxicity in NIH3T3 fibroblasts Rigon, Roberta Balansin [UNESP] Factorial design Fibroblasts MTT assay Skin administration Solid lipid nanoparticles |
title_short |
Solid lipid nanoparticles optimized by 22 factorial design for skin administration: Cytotoxicity in NIH3T3 fibroblasts |
title_full |
Solid lipid nanoparticles optimized by 22 factorial design for skin administration: Cytotoxicity in NIH3T3 fibroblasts |
title_fullStr |
Solid lipid nanoparticles optimized by 22 factorial design for skin administration: Cytotoxicity in NIH3T3 fibroblasts |
title_full_unstemmed |
Solid lipid nanoparticles optimized by 22 factorial design for skin administration: Cytotoxicity in NIH3T3 fibroblasts |
title_sort |
Solid lipid nanoparticles optimized by 22 factorial design for skin administration: Cytotoxicity in NIH3T3 fibroblasts |
author |
Rigon, Roberta Balansin [UNESP] |
author_facet |
Rigon, Roberta Balansin [UNESP] Gonçalez, Maíra Lima [UNESP] Severino, Patrícia Alves, Danilo Antonini Santana, Maria H.A. Souto, Eliana B. Chorilli, Marlus [UNESP] |
author_role |
author |
author2 |
Gonçalez, Maíra Lima [UNESP] Severino, Patrícia Alves, Danilo Antonini Santana, Maria H.A. Souto, Eliana B. Chorilli, Marlus [UNESP] |
author2_role |
author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual Paulista (Unesp) Tiradentes University Universidade Estadual de Campinas (UNICAMP) University of Coimbra (FFUC) University of Coimbra |
dc.contributor.author.fl_str_mv |
Rigon, Roberta Balansin [UNESP] Gonçalez, Maíra Lima [UNESP] Severino, Patrícia Alves, Danilo Antonini Santana, Maria H.A. Souto, Eliana B. Chorilli, Marlus [UNESP] |
dc.subject.por.fl_str_mv |
Factorial design Fibroblasts MTT assay Skin administration Solid lipid nanoparticles |
topic |
Factorial design Fibroblasts MTT assay Skin administration Solid lipid nanoparticles |
description |
The 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. |
publishDate |
2018 |
dc.date.none.fl_str_mv |
2018-12-11T17:21:58Z 2018-12-11T17:21:58Z 2018-11-01 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1016/j.colsurfb.2018.07.065 Colloids and Surfaces B: Biointerfaces, v. 171, p. 501-505. 1873-4367 0927-7765 http://hdl.handle.net/11449/176661 10.1016/j.colsurfb.2018.07.065 2-s2.0-85050850577 2-s2.0-85050850577.pdf 1427125996716282 |
url |
http://dx.doi.org/10.1016/j.colsurfb.2018.07.065 http://hdl.handle.net/11449/176661 |
identifier_str_mv |
Colloids and Surfaces B: Biointerfaces, v. 171, p. 501-505. 1873-4367 0927-7765 10.1016/j.colsurfb.2018.07.065 2-s2.0-85050850577 2-s2.0-85050850577.pdf 1427125996716282 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Colloids and Surfaces B: Biointerfaces 1,071 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
501-505 application/pdf |
dc.source.none.fl_str_mv |
Scopus reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
|
_version_ |
1808129337602342912 |