Comet assay reveals no genotoxicity risk of cationic solid lipid nanoparticles.

Detalhes bibliográficos
Autor(a) principal: Doktorovova, S.
Data de Publicação: 2014
Outros Autores: Silva, A.M., Gaivão, I., Souto, E.B., Teixeira, João Paulo, Martins-Lopes, P.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10400.18/2747
Resumo: Cationic solid lipid nanoparticles (cSLN) are colloidal carriers for genes or drugs, particularly lipophilic drugs. Several reports exist on their high efficiency, but only a few studies report the effect of cSLNs on living cells. In the present work, internalization, cell viability (alamar blue assay) and genotoxic potential (alkaline comet assay) of three cSLN formulations (A–C) were evaluated in HepG2 and Caco-2 cells. cSLN showed an average hydrodynamic diameter (z-ave) of 141–222 nm, zeta-potential of 55.0–72.5mV and polidispersity indices (PdI) of 0.336–0.421. Dispersion in physiological buffers increased z-ave and PdI. 0.01mgml–1 cSLN unaffected cell viability, but 1.0mgml–1 significantly decreased it, being cSLN-C (Compritol-based) the most toxic and HepG2 the most affected. DNA damage was not significantly increased by 0.1mgml–1 cSLN but damage was observed at 1.0mgml–1 cSLN-C. Thus, no genotoxicity is to be expected at concentrations that do not reduce cell viability.
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spelling Comet assay reveals no genotoxicity risk of cationic solid lipid nanoparticles.Comet AssayCaco-2HepG2GenotoxicitySolid Lipid NanoparticlesAr e Saúde OcupacionalGenotoxidade Ambiental e OcupacionalCationic solid lipid nanoparticles (cSLN) are colloidal carriers for genes or drugs, particularly lipophilic drugs. Several reports exist on their high efficiency, but only a few studies report the effect of cSLNs on living cells. In the present work, internalization, cell viability (alamar blue assay) and genotoxic potential (alkaline comet assay) of three cSLN formulations (A–C) were evaluated in HepG2 and Caco-2 cells. cSLN showed an average hydrodynamic diameter (z-ave) of 141–222 nm, zeta-potential of 55.0–72.5mV and polidispersity indices (PdI) of 0.336–0.421. Dispersion in physiological buffers increased z-ave and PdI. 0.01mgml–1 cSLN unaffected cell viability, but 1.0mgml–1 significantly decreased it, being cSLN-C (Compritol-based) the most toxic and HepG2 the most affected. DNA damage was not significantly increased by 0.1mgml–1 cSLN but damage was observed at 1.0mgml–1 cSLN-C. Thus, no genotoxicity is to be expected at concentrations that do not reduce cell viability.Financial support was from Portuguese Science and Technology Foundation (FCT) under reference SFRH/BD/60552/2009 (Doctoral grant to S.D.) and PEst-OE/EQB/LA0023/2011. A.M.S. was supported by European Union Funds (FEDER/COMPETE) and by national funds (FCT) under the project FCOMP-01-0124- FEDER-022696 and by a research project grant (PEst-C/AGR/ UI4033/2011). FCT is also acknowledged under the reference PTDC/SAU-FAR/113100/2009.John Wiley & Sons, LtdRepositório Científico do Instituto Nacional de SaúdeDoktorovova, S.Silva, A.M.Gaivão, I.Souto, E.B.Teixeira, João PauloMartins-Lopes, P.2015-06-01T00:30:06Z2014-042014-04-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.18/2747engJ Appl Toxicol. 2014 Apr;34(4):395-403. doi: 10.1002/jat.2961. Epub 2013 Nov 15.0260-437X10.1002/jat.2961info:eu-repo/semantics/embargoedAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-07-20T15:39:24Zoai:repositorio.insa.pt:10400.18/2747Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T18:37:39.250266Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Comet assay reveals no genotoxicity risk of cationic solid lipid nanoparticles.
title Comet assay reveals no genotoxicity risk of cationic solid lipid nanoparticles.
spellingShingle Comet assay reveals no genotoxicity risk of cationic solid lipid nanoparticles.
Doktorovova, S.
Comet Assay
Caco-2
HepG2
Genotoxicity
Solid Lipid Nanoparticles
Ar e Saúde Ocupacional
Genotoxidade Ambiental e Ocupacional
title_short Comet assay reveals no genotoxicity risk of cationic solid lipid nanoparticles.
title_full Comet assay reveals no genotoxicity risk of cationic solid lipid nanoparticles.
title_fullStr Comet assay reveals no genotoxicity risk of cationic solid lipid nanoparticles.
title_full_unstemmed Comet assay reveals no genotoxicity risk of cationic solid lipid nanoparticles.
title_sort Comet assay reveals no genotoxicity risk of cationic solid lipid nanoparticles.
author Doktorovova, S.
author_facet Doktorovova, S.
Silva, A.M.
Gaivão, I.
Souto, E.B.
Teixeira, João Paulo
Martins-Lopes, P.
author_role author
author2 Silva, A.M.
Gaivão, I.
Souto, E.B.
Teixeira, João Paulo
Martins-Lopes, P.
author2_role author
author
author
author
author
dc.contributor.none.fl_str_mv Repositório Científico do Instituto Nacional de Saúde
dc.contributor.author.fl_str_mv Doktorovova, S.
Silva, A.M.
Gaivão, I.
Souto, E.B.
Teixeira, João Paulo
Martins-Lopes, P.
dc.subject.por.fl_str_mv Comet Assay
Caco-2
HepG2
Genotoxicity
Solid Lipid Nanoparticles
Ar e Saúde Ocupacional
Genotoxidade Ambiental e Ocupacional
topic Comet Assay
Caco-2
HepG2
Genotoxicity
Solid Lipid Nanoparticles
Ar e Saúde Ocupacional
Genotoxidade Ambiental e Ocupacional
description Cationic solid lipid nanoparticles (cSLN) are colloidal carriers for genes or drugs, particularly lipophilic drugs. Several reports exist on their high efficiency, but only a few studies report the effect of cSLNs on living cells. In the present work, internalization, cell viability (alamar blue assay) and genotoxic potential (alkaline comet assay) of three cSLN formulations (A–C) were evaluated in HepG2 and Caco-2 cells. cSLN showed an average hydrodynamic diameter (z-ave) of 141–222 nm, zeta-potential of 55.0–72.5mV and polidispersity indices (PdI) of 0.336–0.421. Dispersion in physiological buffers increased z-ave and PdI. 0.01mgml–1 cSLN unaffected cell viability, but 1.0mgml–1 significantly decreased it, being cSLN-C (Compritol-based) the most toxic and HepG2 the most affected. DNA damage was not significantly increased by 0.1mgml–1 cSLN but damage was observed at 1.0mgml–1 cSLN-C. Thus, no genotoxicity is to be expected at concentrations that do not reduce cell viability.
publishDate 2014
dc.date.none.fl_str_mv 2014-04
2014-04-01T00:00:00Z
2015-06-01T00:30:06Z
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://hdl.handle.net/10400.18/2747
url http://hdl.handle.net/10400.18/2747
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv J Appl Toxicol. 2014 Apr;34(4):395-403. doi: 10.1002/jat.2961. Epub 2013 Nov 15.
0260-437X
10.1002/jat.2961
dc.rights.driver.fl_str_mv info:eu-repo/semantics/embargoedAccess
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dc.publisher.none.fl_str_mv John Wiley & Sons, Ltd
publisher.none.fl_str_mv John Wiley & Sons, Ltd
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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