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首页> 外文期刊>Journal of biomedical nanotechnology >Zinc Oxide Nanoparticles Induce Oxidative Stress and Genotoxicity in Human Liver Cells (HepG2)
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Zinc Oxide Nanoparticles Induce Oxidative Stress and Genotoxicity in Human Liver Cells (HepG2)

机译:氧化锌纳米颗粒在人体肝细胞(HepG2)中引起氧化应激和遗传毒性

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摘要

Zinc oxide (ZnO) is being used worldwide in consumer products and industrial applications. As humans are being directly exposed to ZnO nanoparticles (NPs) through different routes, it is likely that the NPs would gain access to the liver. Therefore, the present study investigated the cytotoxic and genotoxic potential of ZnO nanoparticles in human liver cells (HepG2). The MTT and neutral red uptake assay showed a significant (p < 0.05) concentration and time dependent toxicity after 12 and 24 h at 14 and 20μg/ml. A (p < 0.05) significant increase in DNA damage was observed in cells exposed to ZnO NPs for 6 h as evident with an increase in the Olive tail moment (OTM) and % tail DNA in the Comet assay. The generation of intracellular reactive oxygen species further suggest the role of oxidative stress in ZnO nanoparticle mediated DNA damage and cytotoxicity in HepG2 cells.
机译:氧化锌(ZnO)在全球范围内用于消费产品和工业应用。随着人类通过不同途径直接接触ZnO纳米颗粒(NP),NP可能会进入肝脏。因此,本研究调查了人肝细胞(HepG2)中ZnO纳米颗粒的细胞毒性和遗传毒性潜力。 MTT和中性红吸收试验显示14和20μg/ ml的浓度在12和24小时后具有显着的浓度(p <0.05)和时间依赖性毒性。在暴露于ZnO NPs 6小时的细胞中,观察到DNA损伤显着增加(p <0.05),这在彗星试验中显示出橄榄尾矩(OTM)和尾巴DNA含量增加。细胞内活性氧物种的产生进一步表明氧化应激在ZnO纳米颗粒介导的DNA损伤和HepG2细胞中的细胞毒性中的作用。

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