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Comparing the genotoxicity of a multiwalled carbon nanotube and crocidolite towards the evaluation of its potential impact on the workers’ health

dc.contributor.authorVentura, Célia
dc.contributor.authorSousa Uva, António
dc.contributor.authorSilva, Maria João
dc.date.accessioned2018-02-22T16:40:55Z
dc.date.available2018-02-22T16:40:55Z
dc.date.issued2017-10-03
dc.description.abstractBackground: Multiwalled carbon nanotubes (MWCNT) are one of the most promising and widespread class of manufactured nanomaterials, with several industrial and biomedical applications. However, their unique physicochemical properties may have detrimental effects on human health upon unintentional exposure by inhalation. Although there is still no sufficient epidemiological and toxicological data on most MWCNT, several professional and scientific organizations adopted a precautionary principle and considered MWCNT as an occupational hazard. In vitro toxicological studies can contribute to fulfil the gaps on the knowledge about their potential health adverse effects and to identify biomarkers for human biomonitoring, particularly in the workplace. Aim- This study was aimed at characterizing the cytotoxic and genotoxic effects of NRCWE-006, a high aspect-ratio rigid MWCNT, comparatively to crocidolite, a well-known tumorigenic asbestos fiber causing mesothelioma, using a co-culture of alveolar epithelial cells (A549) and monocyte-derived macrophages (THP-1). Methods – The MTT, the comet and the micronucleus assays were performed on a co-culture of A549 and differentiated THP-1 cells following exposure to a concentration- range of NRCWE-006 or crocidolite. Results- Both NRCWE-006 and crocidolite revealed cytotoxicity by the MTT assay. NRCWE-006 did not induce a detectable level of DNA breaks under the comet assay conditions tested, while a significant increase in the micronucleus frequency was detected at 6.25 and 12.5 µg/cm2. In contrast, crocidolite revealed a clear dose-dependent increase in the level of DNA strand breaks (comet assay) and induced a significant increase in the micronucleus frequency at the highest concentrations tested (10 and 20 µg/cm2). Discussion and Conclusions – Our results suggest that NRCWE-006 is less cytotoxic than crocidolite to alveolar cells grown in co-culture with monocyte-derived macrophages. As expected, crocidolite was clearly genotoxic, given that it was able to induce DNA and chromosome damage, probably due to its known potential of ROS production. On the other hand, even though NRCWE-006 did not cause DNA damage, it demonstrated aneugenic/clastogenic effects at the two lowest concentrations, which are closer to the ones that may represent a concern in terms of occupational exposure.pt_PT
dc.description.sponsorshipThe authors thank to Henriqueta Louro for the technical and scientific support and to Drs. Maria do Carmo Proença and Fátima Aguiar from the Environmental Health Department at INSA for the crocidolite reference material used in this work. This work was co-funded by the Foundation for Science and Technology through the ToxOmics (UID/BIM/00009/2013).pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.urihttp://hdl.handle.net/10400.18/5038
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.subjectGenotoxicidade Ambientalpt_PT
dc.subjectMultiwalled Carbon Nanotubespt_PT
dc.subjectCytotoxicity and Genotoxicitypt_PT
dc.subjectNanomaterialspt_PT
dc.titleComparing the genotoxicity of a multiwalled carbon nanotube and crocidolite towards the evaluation of its potential impact on the workers’ healthpt_PT
dc.typeconference object
dspace.entity.typePublication
oaire.awardURIinfo:eu-repo/grantAgreement/FCT/5876/UID%2FBIM%2F00009%2F2013/PT
oaire.citation.conferencePlaceNápoles, Itáliapt_PT
oaire.citation.title10th International Symposium on Biological Monitoring (ISBM-10), 1-4 October 2017pt_PT
oaire.fundingStream5876
project.funder.identifierhttp://doi.org/10.13039/501100001871
project.funder.nameFundação para a Ciência e a Tecnologia
rcaap.rightsrestrictedAccesspt_PT
rcaap.typeconferenceObjectpt_PT
relation.isProjectOfPublicatione9cc9728-4f09-4e3a-b30d-53d4429986fb
relation.isProjectOfPublication.latestForDiscoverye9cc9728-4f09-4e3a-b30d-53d4429986fb

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