Pyrene-polyethylene glycol-modified multi-walled carbon nanotubes: Genotoxicity in V79-4 fibroblast cells

The genotoxicity of pyrene-polyethylene glycol-modified multi-walled carbon nanotubes (MWCNT-PyPEG), engineered as a nanoplatform for bioapplication, was evaluated. Toxicity was assessed in hamster lung fibroblast cells (V79–4). MTT and Cell Titer Blue methods were used to evaluate cell viability. G...

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Veröffentlicht in:Mutation research. Genetic toxicology and environmental mutagenesis 2022-04, Vol.876-877, p.503463-503463, Article 503463
Hauptverfasser: Ferreira Dantas, Graziela de Paula, Nascimento Martins, Estefânia Mara do, Gomides, Lívia Santos, Chequer, Farah Maria Drumond, Burbano, Rommel Rodríguez, Furtado, Clascídia Aparecida, Santos, Adelina Pinheiro, Tagliati, Carlos Alberto
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Sprache:eng
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Zusammenfassung:The genotoxicity of pyrene-polyethylene glycol-modified multi-walled carbon nanotubes (MWCNT-PyPEG), engineered as a nanoplatform for bioapplication, was evaluated. Toxicity was assessed in hamster lung fibroblast cells (V79–4). MTT and Cell Titer Blue methods were used to evaluate cell viability. Genotoxicity was measured by the comet assay and the cytokinesis-block micronucleus cytome (CBMN-Cyt) assay, and fluorescence in situ hybridization (FISH) was used to test induction of structural chromosome aberrations (clastogenic activity) and/or numerical chromosome changes (aneuploidogenic activity). Exogenous metabolic activation enzymes were used in the CBMN-Cyt and FISH tests. Only with metabolic activation, the hybrids caused chromosomal damage, by both clastogenic and aneugenic processes. •Pyrene-PEG molecules are effective to prepare stable aqueous dispersions of MWCNT.•MWCNT-PyPEG did not cause toxicity in V79-4 cells at tested concentrations.•MWCNT-PyPEG with metabolic activation caused chromosomal damage by aneugenic and clastogenic processes.
ISSN:1383-5718
1879-3592
DOI:10.1016/j.mrgentox.2022.503463