Department of Human Genetics, INSA - National Institute of Health Doutor Ricardo Jorge, I.P, Lisbon, Portugal.
Health Effects Laboratory, Department of Environmental Chemistry, NILU - Norwegian Institute for Air Research, Kjeller, Norway.
Adv Exp Med Biol. 2022;1357:351-375. doi: 10.1007/978-3-030-88071-2_14.
For safety assessment of nanomaterials (NMs), in vitro genotoxicity data based on well-designed experiments is required. Metal-based NMs are amongst the most used in consumer products. In this chapter, we report results for three metal-based NMs, titanium dioxide (NM-100), cerium dioxide (NM-212) and silver (NM-302) in V79 cells, using a set of in vitro genotoxicity assays covering different endpoints: the medium-throughput comet assay and its modified version (with the enzyme formamidopyrimidine DNA glycosylase, Fpg), measuring DNA strand beaks (SBs) and oxidized purines, respectively; the micronucleus (MN) assay, assessing chromosomal damage; and the Hprt gene mutation test. The results generated by this test battery showed that all NMs displayed genotoxic potential. NM-100 induced DNA breaks, DNA oxidation damage and point mutations but not chromosome instability. NM-212 increased the level of DNA oxidation damage, point mutations and increased the MN frequency at the highest concentration tested. NM-302 was moderately cytotoxic and induced gene mutations, but not DNA or chromosome damage. In conclusion, the presented in vitro genotoxicity testing strategy allowed the identification of genotoxic effects caused by three different metal-based NMs, raising concern as to their impact on human health. The results support the use of this in vitro test battery for the genotoxicity assessment of NMs, reducing the use of more expensive, time-consuming and ethically demanding in vivo assays, in compliance with the 3 R's.
为了对纳米材料(NMs)进行安全性评估,需要基于精心设计的实验获得体外遗传毒性数据。金属基纳米材料是在消费产品中使用最多的纳米材料之一。在本章中,我们报告了三种金属基纳米材料(二氧化钛(NM-100)、二氧化铈(NM-212)和银(NM-302)在 V79 细胞中的体外遗传毒性研究结果,使用了一组涵盖不同终点的体外遗传毒性检测方法:中通量彗星试验及其改良版(用酶形式嘧啶 DNA 糖基化酶(Fpg),分别测量 DNA 链缺口(SBs)和氧化嘌呤;微核(MN)试验,评估染色体损伤;和 Hprt 基因突变试验。该测试组合产生的结果表明,所有纳米材料均显示出遗传毒性潜力。NM-100 诱导 DNA 断裂、DNA 氧化损伤和点突变,但不诱导染色体不稳定。NM-212 增加了 DNA 氧化损伤、点突变的水平,并在测试的最高浓度下增加了 MN 频率。NM-302 具有中度细胞毒性,并诱导基因突变,但不诱导 DNA 或染色体损伤。总之,所提出的体外遗传毒性测试策略能够识别三种不同金属基纳米材料引起的遗传毒性效应,引起对其对人类健康影响的关注。这些结果支持使用该体外测试组合对纳米材料的遗传毒性进行评估,从而减少对更昂贵、耗时和更具伦理要求的体内试验的使用,符合 3R 原则。