Please use this identifier to cite or link to this item: https://hdl.handle.net/10216/149448
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dc.creatorBessa, MJ
dc.creatorBrandão, F
dc.creatorFokkens, PHB
dc.creatorLeseman, DLAC
dc.creatorBoere, AJF
dc.creatorCassee, FR
dc.creatorSalmatonidis, A
dc.creatorViana, M
dc.creatorVulpoi, A
dc.creatorSimon, S
dc.creatorMonfort, E
dc.creatorTeixeira, JP
dc.creatorFraga, S
dc.date.accessioned2023-05-23T14:22:58Z-
dc.date.available2023-05-23T14:22:58Z-
dc.date.issued2021
dc.identifier.issn2079-4991
dc.identifier.urihttps://hdl.handle.net/10216/149448-
dc.description.abstractDiverse industries have already incorporated within their production processes engineered nanoparticles (ENP), increasing the potential risk of worker inhalation exposure. In vitro models have been widely used to investigate ENP toxicity. Air–liquid interface (ALI) cell cultures have been emerging as a valuable alternative to submerged cultures as they are more representative of the inhalation exposure to airborne nano-sized particles. We compared the in vitro toxicity of four ENP used as raw materials in the advanced ceramics sector in human alveolar epithelial-like cells cultured under submerged or ALI conditions. Submerged cultures were exposed to ENP liquid suspensions or to aerosolised ENP at ALI. Toxicity was assessed by determining LDH release, WST-1 metabolisation and DNA damage. Overall, cells were more sensitive to ENP cytotoxic effects when cultured and exposed under ALI. No significant cytotoxicity was observed after 24 h exposure to ENP liquid suspensions, although aerosolised ENP clearly affected cell viability and LDH release. In general, all ENP increased primary DNA damage regardless of the exposure mode, where an increase in DNA strand-breaks was only detected under submerged conditions. Our data show that at relevant occupational concentrations, the selected ENP exert mild toxicity to alveolar epithelial cells and exposure at ALI might be the most suitable choice when assessing ENP toxicity in respiratory models under realistic exposure conditions.
dc.description.sponsorshipThis research was funded by CERASAFE (www.cerasafe.eu; accessed on 26 October 2021), with the support of ERA-NET SIINN (project id:16) and the Portuguese Foundation for Science and Technology (FCT; SIINN/0004/2014). This work was also supported by the NanoBioBarriers project (PTDC/MED-TOX/31162/2017), co-financed by the Operational Program for Competitiveness and Internationalization (POCI) through European Regional Development Funds (FEDER/FNR) and FCT; Spanish Ministry of Science and Innovation (projects PCIN-2015-173-C02-01 and CEX2018-000794-S-Severo Ochoa), and by the Romanian National Authority for Scientific Research and Innovation (CCCDI-UEFISCDI, project number 29/2016 within PNCDI III). M.J. Bessa (SFRH/BD/120646/2016) and F. Brandão (SFRH/BD/101060/2014) are recipients of FCT PhD scholarships under the framework of Human Capital Operating Program (POCH) and European Union funding. The Doctoral Program in Biomedical Sciences, of the ICBAS—University of Porto, offered additional funds. S. Fraga thanks FCT for funding through program DL 57/2016–Norma transitória (Ref. DL-57/INSA-06/2018). Thanks are also due to FCT/MCTES for the financial support to EPIUnit (info:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDB/04750/2020/PT).
dc.language.isoeng
dc.publisherMDPI
dc.relationinfo:eu-repo/grantAgreement/FCT/9471 - RIDTI/PTDC/MED-TOX/31162/2017/PT/PT
dc.relationinfo:eu-repo/grantAgreement/FCT/POR_NORTE/SFRH/BD/120646/2016/PT
dc.relationinfo:eu-repo/grantAgreement/FCT/OE/SFRH/BD/101060/2014/PT
dc.relationinfo:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDB/04750/2020/PT
dc.relation.ispartofNanomaterials (Basel). 2021 Nov 27;11(12):3225
dc.rightsopenAccess
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subjectengineered nanoparticles
dc.subjectsubmerged cultures
dc.subjectair-liquid interface
dc.subjectin vitro cytotoxicity
dc.subjectDNA damage
dc.subjectgenotoxicity
dc.titleIn Vitro Toxicity of Industrially Relevant Engineered Nanoparticles in Human Alveolar Epithelial Cells: Air-Liquid Interface versus Submerged Cultures
dc.typeArtigo em Revista Científica Internacional
dc.contributor.uportoInstituto de Saúde Pública da Universidade do Porto
dc.identifier.doi10.3390/nano11123225
dc.relation.publisherversionhttps://www.mdpi.com/2079-4991/11/12/3225
Appears in Collections:ISPUP - Artigo em Revista Científica Internacional

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