Toxicology Lab, Applied Biology Division, CSIR-Indian Institute of Chemical Technology, Hyderabad, Telangana, India.
Academy of Scientific and Innovative Research, CSIR-Indian Institute of Chemical Technology, Hyderabad, Telangana, India.
J Appl Toxicol. 2019 Jul;39(7):955-965. doi: 10.1002/jat.3784. Epub 2019 Feb 14.
The current study was intended to elucidate the cytotoxicity, genotoxicity ability of nickel oxide (NiO) nanoparticles (NPs) and assessment of preliminary mechanism of the toxicity. Characterization studies showed that NiO-NPs have a particle size of 17.94 (±3.48) nm. The particle size of the NPs obtained by dynamic light scattering method in Milli-Q and RPMI 1640 media was 189.9 (±17.1) and 285.9 (±19.6) nm, respectively. The IC concentration for NiO-NPs after 24 hours of treatment was estimated as 23.58 μg/mL. Comet and cytokinesis-block micronucleus assays revealed a significant dose- and time-dependent genotoxic potential of NiO-NPs. Morphological assessment of the lymphocytes upon exposure to NiO-NPs showed that the mechanism of toxicity was apoptosis. Reactive oxygen species analysis and lipid peroxidation patterns were aligned with the cytotoxicity and genotoxicity endpoints. Thus, the preliminary mechanism of NiO-NPs for cytotoxicity on lymphocytes was assumed to be oxidative stress-mediated apoptosis and DNA damage. Furthermore, these NiO-NPs are considered a potentially hazardous substance at environmentally significant levels. Further investigations are suggested to understand the immunotoxic effects of NiO-NPs.
本研究旨在阐明氧化镍(NiO)纳米粒子(NPs)的细胞毒性和遗传毒性能力,并评估其毒性的初步机制。表征研究表明,NiO-NPs 的粒径为 17.94(±3.48)nm。动态光散射法在 Milli-Q 和 RPMI 1640 培养基中测得的 NPs 粒径分别为 189.9(±17.1)和 285.9(±19.6)nm。NiO-NPs 处理 24 小时后的 IC 浓度估计为 23.58μg/mL。彗星和胞质分裂阻断微核试验显示 NiO-NPs 具有显著的剂量和时间依赖性遗传毒性潜力。暴露于 NiO-NPs 后淋巴细胞的形态评估表明,毒性机制是细胞凋亡。活性氧分析和脂质过氧化模式与细胞毒性和遗传毒性终点一致。因此,NiO-NPs 对淋巴细胞的细胞毒性的初步机制被假设为氧化应激介导的细胞凋亡和 DNA 损伤。此外,这些 NiO-NPs 被认为是在具有重要环境意义的水平上具有潜在危害性的物质。建议进行进一步的研究以了解 NiO-NPs 的免疫毒性作用。