Repository logo
 
Publication

Comparative Analysis of the Toxicity Profile of Eleven Consumer-Relevant Nanomaterials in Human Intestinal and Placental Barrier Cells

dc.contributor.authorPires, Joana
dc.contributor.authorMoreira, Luciana
dc.contributor.authorTeixeira, João Paulo
dc.contributor.authorFraga, Sónia
dc.date.accessioned2023-10-09T15:05:54Z
dc.date.available2023-10-09T15:05:54Z
dc.date.issued2023-04-21
dc.description.abstractBackground: The growing number of items incorporating nanomaterials (NM) has prompted considerable concerns about human health and safety [1]. Metal nanoparticles, inorganic non-metallic, and carbon-based NM are among the types with the highest market volume [2]. Objective: The purpose of this study was to determine the effect of chemical composition [Ag, Au, TiO2, SiO2, and graphene oxide (nano_GO)], primary size (10, 30 and 60 nm AgNP and AuNP), crystal structure (TiO2NP rutile/anatase and anatase), and surface coating (citrate and PEGylated AuNP) on potential toxicity to human intestinal (Caco-2) and placental (BeWo b30) epithelial cells. Methods: Changes in cell morphology, metabolic activity, plasma membrane integrity, intracellular ROS and ATP levels, and DNA integrity were assessed to investigate their potential toxicity at 24 h after exposure. Results: In both barrier models, the toxicity profile was similar, however placentalwere more sensitive than intestinal epithelial cells. Overall, NM may be ranked for cytotoxicity as AgNP > nano_GO > AuNP ~ TiO2NP ~ SiO2NP, with the effects becoming more evident at greater concentrations. The influence of size was more pronounced for AgNP than for AuNP, with the smaller nanoparticles producing higher cytotoxic effects. The cytotoxicity of AuNP was prevented by PEG capping. AgNP and nano_GO exposure markedly raised the levels of ROS, indicating that oxidative stress may play a role in their cytotoxicity. Except for 10 nm AuNP, every NM tested markedly increased intracellular ATP levels. One interesting finding was that a higher cytotoxic potential did not necessarily equate to a higher genotoxic potential, since only AgNP (classified as positive) and anatase TiO2NP (classified as equivocal) caused DNA damage. Conclusions: Our findings alert to the potential risks associated with human barriers exposure to NM, where the physicochemical properties are important determinants of their toxicity. Additional research is needed for a deeper understanding of NM impact on human barriers.pt_PT
dc.description.sponsorshipThis research was funded by the project NanoBioBarriers, grant number PTDC/MED‐TOX/31162/2017, co-financed by the Operational Program for Competitiveness and Internationalization (POCI) through European Regional Development Funds (FEDER/FNR) and the Foundation for Science and Technology (FCT/MCTES). This work is financed by national funds through FCT – Foundation for Science and Technology within the scope of projects UIDB/04750/2020 and LA/P/0064/2020.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationScientific Letters. 2023;1(Sup 1). Epub. 2023 Apr 21. https://doi.org/10.48797/sl.2023.47pt_PT
dc.identifier.doi10.48797/sl.2023.47pt_PT
dc.identifier.issn2795-5117
dc.identifier.urihttp://hdl.handle.net/10400.18/8679
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.relationNanoBioBarriers PTDC/MED‐TOX/31162/2017pt_PT
dc.relationEpidemiology Research Unit - Institute of Public Health, University of Porto
dc.relation.publisherversionhttps://publicacoes.cespu.pt/index.php/sl/article/view/47pt_PT
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt_PT
dc.subjectNanomaterialspt_PT
dc.subjectHuman Intestinalpt_PT
dc.subjectPlacental Barrier Cellpt_PT
dc.subjectin vitro Toxicitypt_PT
dc.subjectCaco-2 Cellspt_PT
dc.subjectBeWo b30 Cellpt_PT
dc.subjectGenotoxicidade Ambientalpt_PT
dc.titleComparative Analysis of the Toxicity Profile of Eleven Consumer-Relevant Nanomaterials in Human Intestinal and Placental Barrier Cellspt_PT
dc.typeconference object
dspace.entity.typePublication
oaire.awardTitleEpidemiology Research Unit - Institute of Public Health, University of Porto
oaire.awardURIinfo:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDB%2F04750%2F2020/PT
oaire.citation.conferencePlacePorto, Portugalpt_PT
oaire.citation.issue(Sup 1)pt_PT
oaire.citation.titleII TOXRUN International Congress, 27-28 April 2023pt_PT
oaire.citation.volume1pt_PT
oaire.fundingStream6817 - DCRRNI ID
project.funder.identifierhttp://doi.org/10.13039/501100001871
project.funder.nameFundação para a Ciência e a Tecnologia
rcaap.rightsopenAccesspt_PT
rcaap.typeconferenceObjectpt_PT
relation.isProjectOfPublication05f4f337-eeba-4c07-82ed-4202b21618a2
relation.isProjectOfPublication.latestForDiscovery05f4f337-eeba-4c07-82ed-4202b21618a2

Files

Original bundle
Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
Pires et al_2023.pdf
Size:
291.63 KB
Format:
Adobe Portable Document Format
License bundle
Now showing 1 - 1 of 1
No Thumbnail Available
Name:
license.txt
Size:
1.71 KB
Format:
Item-specific license agreed upon to submission
Description: