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In vitro toxicity evaluation of silica-coated iron oxide nanoparticles in human SHSY5Y neuronal cells

dc.contributor.authorKiliç, Gözde
dc.contributor.authorCosta, Carla
dc.contributor.authorFernández-Bertólez, Natalia
dc.contributor.authorPásaro, Eduardo
dc.contributor.authorTeixeira, João Paulo
dc.contributor.authorLaffon, Blanca
dc.contributor.authorValdiglesias, Vanessa
dc.date.accessioned2016-02-16T17:42:14Z
dc.date.available2016-02-16T17:42:14Z
dc.date.issued2015-10-23
dc.description.abstractIron oxide nanoparticles (ION) have been widely used in biomedical applications, for both diagnosis and therapy, due to their unique magnetic properties. They are intensively explored in neuromedicine mostly because of their ability to cross the blood brain barrier. Hence, their potential harmful effects on neuronal cells need to be carefully assessed. The objective of this study was to evaluate the toxicity of silica-coated ION (S-ION) (10–200 μg ml−1) on human neuronal SHSY5Y cells. Alterations in the cell cycle, cell death by apoptosis or necrosis, and membrane integrity were assessed as cytotoxicity parameters. Genotoxicity was determined by a γH2AX assay, a micronucleus (MN) test, and a comet assay. Complementarily, possible effects on DNA damage repair were also analysed by means of a DNA repair competence assay. All analyses were performed in complete and serum-free cell culture media. Iron ion release from the nanoparticles was notable only in complete medium. Despite being effectively internalized by the neuronal cells, S-ION presented in general low cytotoxicity; positive results were only obtained in some assays at the highest concentrations and/or the longest exposure time tested (24 h). Genotoxicity evaluations in serum-free medium were negative for all conditions assayed; in complete medium, dose and time-dependent increase in DNA damage not related to the production of double strand breaks or chromosome loss (according to the results of the γH2AX assay and MN test), was obtained. The presence of serum slightly influenced the behaviour of S-ION; further studies to investigate the formation of a protein corona and its role in nanoparticle toxicity are necessary.pt_PT
dc.description.sponsorshipThis work was funded by Xunta de Galicia (EM 2012/079) and by TD1204 MODENA COST Action. G. Kiliç was supported by a fellowship from the University of A Coruña.pt_PT
dc.identifier.citationToxicol. Res. 2016; 5: 235-47. doi:10.1039/C5TX00206K. Epub 2015 Oct 23pt_PT
dc.identifier.doi10.1039/C5TX00206Kpt_PT
dc.identifier.issn2045-4538
dc.identifier.urihttp://hdl.handle.net/10400.18/3349
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherRoyal Society of Chemistrypt_PT
dc.relation.publisherversionhttp://pubs.rsc.org/en/Content/ArticleLanding/2016/TX/C5TX00206K#!divAbstractpt_PT
dc.subjectIron Oxide Nanoparticlespt_PT
dc.subjectGenotoxicitypt_PT
dc.subjectCytotoxicitypt_PT
dc.subjectDNA Eepair
dc.subjectSHSY5Y cells
dc.subjectGenotoxicidade Ambiental
dc.titleIn vitro toxicity evaluation of silica-coated iron oxide nanoparticles in human SHSY5Y neuronal cellspt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage247pt_PT
oaire.citation.startPage235pt_PT
oaire.citation.titleToxicology Researchpt_PT
oaire.citation.volume5pt_PT
rcaap.rightsembargoedAccesspt_PT
rcaap.typearticlept_PT

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