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Moving into advanced nanomaterials. Toxicity of rutile TiO2 nanoparticles immobilized in nanokaolin nanocomposites on HepG2 cell line

dc.contributor.authorBessa, Maria João
dc.contributor.authorCosta, Carla
dc.contributor.authorReinosa, Julian
dc.contributor.authorPereira, Cristiana
dc.contributor.authorFraga, Sónia
dc.contributor.authorFernández, José
dc.contributor.authorBañares, Miguel A.
dc.contributor.authorTeixeira, João Paulo
dc.date.accessioned2017-03-09T17:00:15Z
dc.date.available2022-12-29T01:30:15Z
dc.date.issued2016-12-28
dc.description.abstractImmobilization of nanoparticles on inorganic supports has been recently developed, resulting in the creation of nanocomposites. Concerning titanium dioxide nanoparticles (TiO2 NPs(1)), these have already been developed in conjugation with clays, but so far there are no available toxicological studies on these nanocomposites. The present work intended to evaluate the hepatic toxicity of nanocomposites (C-TiO2(2)), constituted by rutile TiO2 NPs immobilized in nanokaolin (NK(3)) clay, and its individual components. These nanomaterials were analysed by means of FE-SEM(4) and DLS(5) analysis for physicochemical characterization. HepG2 cells were exposed to rutile TiO2 NPs, NK clay and C-TiO2 nanocomposite, in the presence and absence of serum for different exposure periods. Possible interferences with the methodological procedures were determined for MTT,(6) neutral red uptake, alamar blue (AB), LDH,(7) and comet assays, for all studied nanomaterials. Results showed that MTT, AB and alkaline comet assay were suitable for toxicity analysis of the present materials after slight modifications to the protocol. Significant decreases in cell viability were observed after exposure to all studied nanomaterials. Furthermore, an increase in HepG2 DNA damage was observed after shorter periods of exposure in the absence of serum proteins and longer periods of exposure in their presence. Although the immobilization of nanoparticles in micron-sized supports could, in theory, decrease the toxicity of single nanoparticles, the selection of a suitable support is essential. The present results suggest that NK clay is not the appropriate substrate to decrease TiO2 NPs toxicity. Therefore, for future studies, it is critical to select a more appropriate substrate for the immobilization of TiO2 NPs.pt_PT
dc.description.sponsorshipThis research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors. Notwithstanding, we would like to acknowledge TD1204 MODENA COST Action for supporting this work.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationToxicol Appl Pharmacol. 2017 Feb 1;316:114-122. doi: 10.1016/j.taap.2016.12.018. Epub 2016 Dec 28pt_PT
dc.identifier.doi10.1016/j.taap.2016.12.018pt_PT
dc.identifier.issn0041-008X
dc.identifier.urihttp://hdl.handle.net/10400.18/4591
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherElsevier/ Academic Presspt_PT
dc.relation.publisherversionhttp://www.sciencedirect.com/science/article/pii/S0041008X16303970pt_PT
dc.subjectCytotoxicitypt_PT
dc.subjectGenotoxicitypt_PT
dc.subjectIn vitropt_PT
dc.subjectInterferences Studiespt_PT
dc.subjectKaolin Nanoclaypt_PT
dc.subjectTitanium Dioxide Nanoparticlespt_PT
dc.subjectGenotoxicidade Ambientalpt_PT
dc.titleMoving into advanced nanomaterials. Toxicity of rutile TiO2 nanoparticles immobilized in nanokaolin nanocomposites on HepG2 cell linept_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage122pt_PT
oaire.citation.startPage114pt_PT
oaire.citation.titleToxicology and Applied Pharmacologypt_PT
oaire.citation.volume316pt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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