Division of Biomedical Sciences, University of Bradford, Richmond Road, Bradford, West Yorkshire, BD7 1DP, UK.
Nanomedicine (Lond). 2010 Oct;5(8):1193-203. doi: 10.2217/nnm.10.52.
The rapidly growing industrial and medical use of nanomaterials, especially zinc oxide and titanium dioxide, has led to growing concerns about their toxicity. Accordingly, the intrinsic genotoxic and cytotoxic potential of these nanoparticles have been evaluated.
MATERIALS & METHODS: Using a HEp-2 cell line, cytotoxicity was tested along with mitochondrial activity and neutral red uptake assays. The genotoxic potential was determined using the Comet and the cytokinesis-blocked micronucleus assays. In addition, tyrosine phosphorylation events were investigated.
RESULTS & CONCLUSION: We found concentration- and time-dependent cytotoxicity and an increase in DNA and cytogenetic damage with increasing nanoparticle concentrations. Mainly for zinc oxide, genotoxicity was clearly associated with an increase in tyrosine phosphorylation. Our results suggest that both types of nanoparticles can be genotoxic over a range of concentrations without being cytotoxic.
纳米材料,尤其是氧化锌和二氧化钛,在工业和医疗领域的应用迅速增长,这引发了人们对其毒性的日益关注。因此,人们评估了这些纳米粒子的固有遗传毒性和细胞毒性。
使用 HEp-2 细胞系,通过线粒体活性和中性红摄取试验检测细胞毒性。通过彗星试验和胞质分裂阻断微核试验测定遗传毒性潜能。此外,还研究了酪氨酸磷酸化事件。
我们发现细胞毒性与浓度和时间呈依赖性,且随着纳米粒子浓度的增加,DNA 和细胞遗传损伤增加。主要针对氧化锌,遗传毒性与酪氨酸磷酸化的增加明显相关。我们的结果表明,这两种类型的纳米粒子在无细胞毒性的浓度范围内可能具有遗传毒性。