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使用人体体外模型对两种原始碳纳米材料(氧化石墨烯和氨基化氧化石墨烯)及其相应降解形式进行比较毒理学分析。

Comparative toxicological analysis of two pristine carbon nanomaterials (graphene oxide and aminated graphene oxide) and their corresponding degraded forms using human in vitro models.

机构信息

International Research Center in Critical Raw Materials for Advanced Industrial Technologies-ICCRAM, Universidad de Burgos, Plaza Misael Bañuelos s/n, Burgos 09001, Spain.

Department of Chemical, Physics, Mathematics and Natural Science, University of Sassari, Via Vienna 2, Sassari 07100, Italy.

出版信息

Toxicology. 2024 May;504:153783. doi: 10.1016/j.tox.2024.153783. Epub 2024 Mar 20.

DOI:10.1016/j.tox.2024.153783
PMID:38518840
Abstract

Despite the wide application of graphene-based materials, the information of the toxicity associated to some specific derivatives such as aminated graphene oxide is scarce. Likewise, most of these studies analyse the pristine materials, while the available data regarding the harmful effects of degraded forms is very limited. In this work, the toxicity of graphene oxide (GO), aminated graphene oxide (GO-NH), and their respective degraded forms (dGO and dGO-NH) obtained after being submitted to high-intensity sonication was evaluated applying in vitro assays in different models of human exposure. Viability and ROS assays were performed on A549 and HT29 cells, while their skin irritation potential was tested on a reconstructed human epidermis model. The obtained results showed that GO-NH and dGO-NH substantially decrease cell viability in the lung and gastrointestinal models, being this reduction slightly higher in the cells exposed to the degraded forms. In contrast, this parameter was not affected by GO and dGO which, conversely, showed the ability to induce higher levels of ROS than the pristine and degraded aminated forms. Furthermore, none of the materials is skin irritant. Altogether, these results provide new insights about the potential harmful effects of the selected graphene-based nanomaterials in comparison with their degraded counterparts.

摘要

尽管基于石墨烯的材料得到了广泛的应用,但有关某些特定衍生物(如氨基化氧化石墨烯)毒性的信息却很少。同样,这些研究大多分析的是原始材料,而关于降解形式的有害影响的数据非常有限。在这项工作中,评估了经过高强度超声处理后获得的氧化石墨烯(GO)、氨基化氧化石墨烯(GO-NH)及其相应降解形式(dGO 和 dGO-NH)的毒性,通过不同的人体暴露模型进行了体外检测。在 A549 和 HT29 细胞上进行了细胞活力和 ROS 测定,而在重建的人体表皮模型上测试了其皮肤刺激性潜力。结果表明,GO-NH 和 dGO-NH 显著降低了肺和胃肠道模型中的细胞活力,而降解形式暴露的细胞中的这种降低更为明显。相比之下,GO 和 dGO 并未影响这一参数,而这两种物质反而显示出比原始和降解的氨基化形式诱导更高水平 ROS 的能力。此外,这些材料都没有皮肤刺激性。总之,这些结果为比较所选基于石墨烯的纳米材料及其降解对应物的潜在有害影响提供了新的见解。

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