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采用彗星和 SMART 试验评估不同粒径金纳米粒子的体外和体内遗传毒性。

In vitro and in vivo genotoxicity assessment of gold nanoparticles of different sizes by comet and SMART assays.

机构信息

Departamento de Nutrición, Bromatología y Tecnología de los Alimentos, Facultad de Veterinaria, Universidad Complutense de Madrid, 28040, Madrid, Spain.

Departamento de Nutrición, Bromatología y Tecnología de los Alimentos, Facultad de Veterinaria, Universidad Complutense de Madrid, 28040, Madrid, Spain.

出版信息

Food Chem Toxicol. 2018 Oct;120:81-88. doi: 10.1016/j.fct.2018.06.061. Epub 2018 Jun 28.

Abstract

Due to the increasing use of gold nanoparticles (AuNPs) in different areas such as medicine, biotechnology or food sector, human exposure to them has grown significantly and its toxicity evaluation has become essential. Therefore, the purpose of this study was to compare the potential genotoxic effects of 30, 50 and 90 nm AuNPs, using in vitro comet assay with the in vivo mutagenic and recombinogenic activity (SMART Test) in Drosophila. The results indicated that in both cell lines, 30, 50 and 90 nm (1-10 μg ml) AuNPs increased DNA strand breaks following 24 h treatment. This damage was not dose and size-dependent. Moreover, a modified comet assay using endonuclease III and formamidopyrimidine-DNA glycosylase restriction enzymes showed that in both cell lines, pyrimidines and purines were oxidatively damaged by all AuNPs, being 90 nm AuNPs slightly more genotoxic. However, the data obtained with SMART showed that 30 nm AuNPs did not modify the spontaneous frequencies of spots indicating lack of mutagenic and recombinogenic activity. Therefore, further experiments must be carried out to gain a better understanding of the mechanism of action of AuNPs to ensure their safe use.

摘要

由于金纳米粒子(AuNPs)在医学、生物技术或食品等不同领域的应用越来越广泛,人类接触 AuNPs 的情况显著增加,对其毒性的评估变得至关重要。因此,本研究旨在比较 30、50 和 90nm AuNPs 的潜在遗传毒性效应,使用体外彗星试验和体内诱变和重组活性(SMART 试验)在果蝇中进行。结果表明,在两种细胞系中,30、50 和 90nm(1-10μg/ml)AuNPs 在 24 小时处理后均增加了 DNA 链断裂。这种损伤与剂量和尺寸无关。此外,使用内切酶 III 和 5- 甲基胞嘧啶-DNA 糖基化酶限制酶的改良彗星试验表明,在两种细胞系中,嘧啶和嘌呤均被所有 AuNPs 氧化损伤,90nm AuNPs 的遗传毒性略高。然而,SMART 获得的数据表明,30nm AuNPs 没有改变指示缺乏诱变和重组活性的自发斑点频率。因此,必须进行进一步的实验,以更好地了解 AuNPs 的作用机制,确保其安全使用。

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