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Determination of mutagenicity and genotoxicity of indium tin oxide nanoparticles using the Ames test and micronucleus assay

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dc.creator Eren, Yasin
dc.creator AKYIL, DİLEK
dc.creator KONUK, MUHSİN
dc.creator Tepekozcan, Aykut
dc.creator Saglam, Esra
dc.date 2016-08-31T21:00:00Z
dc.date.accessioned 2020-10-06T11:23:08Z
dc.date.available 2020-10-06T11:23:08Z
dc.identifier c70fdece-37a2-4045-9be4-2643e25b0ce3
dc.identifier 10.1177/0748233715579804
dc.identifier https://avesis.sdu.edu.tr/publication/details/c70fdece-37a2-4045-9be4-2643e25b0ce3/oai
dc.identifier.uri http://acikerisim.sdu.edu.tr/xmlui/handle/123456789/71718
dc.description In this study, the mutagenicity and genotoxicity of indium tin oxide (ITO) nanomaterial were assessed using two standard genotoxicity assays, the Salmonella reverse mutation assay (Ames test) and the in vitro micronucleus (MN) assay. Seven different concentrations (12.5, 25, 50, 75, 100, 125, and 150 mu g/plate) of this nanomaterial were tested using the Ames test on the TA98 and TA100 strains in the presence and absence of the S9 mixture. At all the concentrations tested, this substance did not significantly increase the number of revertant colonies compared with the control with or without S9 mixture. The genotoxic effects of ITO were investigated in human peripheral lymphocytes treated with 125, 250, 500, and 750 mu g/ml concentrations of this substance for 24- and 48-h treatment periods using an MN test. Nuclear division index (NDI) was also calculated in order to determine the cytotoxicity of ITO. It was determined that ITO increased MN frequency in the 750 mu g/ml concentration in 24- and 48-h treatments. In addition, ITO dose dependently decreased the NDI significantly for two treatment periods.
dc.language eng
dc.rights info:eu-repo/semantics/closedAccess
dc.title Determination of mutagenicity and genotoxicity of indium tin oxide nanoparticles using the Ames test and micronucleus assay
dc.type info:eu-repo/semantics/article


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