Bundesanstalt für Materialforschung und -prüfung (BAM), Division 1.2 Biophotonics, Richard-Willstätter-Str. 11, 12489 Berlin, Germany.
Fraunhofer-Zentrum für Angewandte Nanotechnologie CAN, Grindelallee 117, 20146 Hamburg, Germany.
Nanoscale. 2019 Jul 18;11(28):13458-13468. doi: 10.1039/c9nr01021a.
The large number of nanomaterial-based applications emerging in the materials and life sciences and the foreseeable increasing use of these materials require methods that evaluate and characterize the toxic potential of these nanomaterials to keep safety risks to people and environment as low as possible. As nanomaterial toxicity is influenced by a variety of parameters like size, shape, chemical composition, and surface chemistry, high throughput screening (HTS) platforms are recommended for assessing cytotoxicity. Such platforms are not yet available for genotoxicity testing. Here, we present first results obtained for application-relevant nanomaterials using an automatable genotoxicity platform that relies on the quantification of the phosphorylated histone H2AX (γ-H2AX) for detecting DNA double strand breaks (DSBs) and the automated microscope system AKLIDES® for measuring integral fluorescence intensities at different excitation wavelengths. This platform is used to test the genotoxic potential of 30 nm-sized citrate-stabilized gold nanoparticles (Au-NPs) as well as micellar encapsulated iron oxide nanoparticles (FeOx-NPs) and different cadmium (Cd)-based semiconductor quantum dots (QDs), thereby also searching for positive and negative controls as reference materials. In addition, the influence of the QD shell composition on the genotoxic potential of these Cd-based QDs was studied, using CdSe cores as well as CdSe/CdS core/shell and CdSe/CdS/ZnS core/shell/shell QDs. Our results clearly revealed the genotoxicity of the Au-NPs and its absence in the FeOx-NPs. The genotoxicity of the Cd-QDs correlates with the shielding of their Cd-containing core, with the core/shell/shell architecture preventing genotoxicity risks. The fact that none of these nanomaterials showed cytotoxicity at the chosen particle concentrations in a conventional cell viability assay underlines the importance of genotoxicity studies to assess the hazardous potential of nanomaterials.
大量新兴的基于纳米材料的应用出现在材料和生命科学领域,预计这些材料的使用将会增加,因此需要方法来评估和描述这些纳米材料的毒性潜力,以将对人和环境的安全风险降至最低。由于纳米材料的毒性受多种参数的影响,如大小、形状、化学成分和表面化学性质,因此建议使用高通量筛选(HTS)平台来评估细胞毒性。目前还没有用于遗传毒性测试的此类平台。在这里,我们使用一种自动化遗传毒性平台,该平台基于定量检测 DNA 双链断裂(DSBs)的磷酸化组蛋白 H2AX(γ-H2AX),以及用于测量不同激发波长下积分荧光强度的自动化显微镜系统 AKLIDES®,来展示应用相关纳米材料的初步结果。该平台用于测试 30nm 大小的柠檬酸稳定金纳米颗粒(Au-NPs)以及胶束包封的氧化铁纳米颗粒(FeOx-NPs)和不同的基于镉(Cd)的半导体量子点(QDs)的遗传毒性潜力,从而还寻找阳性和阴性对照物质作为参考材料。此外,还研究了 QD 壳层组成对这些 Cd 基 QDs 遗传毒性潜力的影响,使用 CdSe 核以及 CdSe/CdS 核/壳和 CdSe/CdS/ZnS 核/壳/壳 QDs。我们的结果清楚地揭示了 Au-NPs 的遗传毒性及其在 FeOx-NPs 中的缺失。Cd-QDs 的遗传毒性与它们含 Cd 核心的屏蔽有关,具有核/壳/壳结构的 QDs 可防止遗传毒性风险。在传统的细胞活力测定中,选择的颗粒浓度下,这些纳米材料均未显示出细胞毒性,这突出了遗传毒性研究在评估纳米材料的危害性潜力方面的重要性。