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采用不同暴露途径的人源体外模型对具有增强电化学性能的氧化锰纳米材料进行毒理学评估。

Toxicology assessment of manganese oxide nanomaterials with enhanced electrochemical properties using human in vitro models representing different exposure routes.

机构信息

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

Gnanomat S.L., Campus Cantoblanco, Madrid Science Park, c/ Faraday 7, 28049, Madrid, Spain.

出版信息

Sci Rep. 2022 Dec 5;12(1):20991. doi: 10.1038/s41598-022-25483-w.


DOI:10.1038/s41598-022-25483-w
PMID:36471154
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9723098/
Abstract

In the present study, a comparative human toxicity assessment between newly developed MnO nanoparticles with enhanced electrochemical properties (GNA35) and their precursor material (MnO) was performed, employing different in vitro cellular models representing main exposure routes (inhalation, intestinal and dermal contact), namely the human alveolar carcinoma epithelial cell line (A549), the human colorectal adenocarcinoma cell line (HT29), and the reconstructed 3D human epidermal model EpiDerm. The obtained results showed that MnO and GNA35 harbour similar morphological characteristics, whereas differences were observed in relation to their surface area and electrochemical properties. In regard to their toxicological properties, both nanomaterials induced ROS in the A549 and HT29 cell lines, while cell viability reduction was only observed in the A549 cells. Concerning their skin irritation potential, the studied nanomaterials did not cause a reduction of the skin tissue viability in the test conditions nor interleukin 1 alpha (IL- 1 α) release. Therefore, they can be considered as not irritant nanomaterials according to EU and Globally Harmonized System of Classification and Labelling Chemicals. Our findings provide new insights about the potential harmful effects of MnO nanomaterials with different properties, demonstrating that the hazard assessment using different human in vitro models is a critical aspect to increase the knowledge on their potential impact upon different exposure routes.

摘要

在本研究中,对具有增强电化学性能的新型 MnO 纳米粒子(GNA35)与其前体材料(MnO)进行了比较人体毒性评估,采用了不同的代表主要暴露途径(吸入、肠道和皮肤接触)的体外细胞模型,即人肺泡癌细胞系(A549)、人结直肠腺癌细胞系(HT29)和重建的 3D 人表皮模型 EpiDerm。研究结果表明,MnO 和 GNA35 具有相似的形态特征,但在表面积和电化学性能方面存在差异。在毒理学特性方面,两种纳米材料均在 A549 和 HT29 细胞系中诱导了 ROS,而只有 A549 细胞的细胞活力降低。关于它们的皮肤刺激性潜力,研究中的纳米材料在测试条件下没有导致皮肤组织活力降低,也没有导致白细胞介素 1 阿尔法(IL-1α)释放。因此,根据欧盟和全球化学品统一分类和标签制度,它们可以被认为是无刺激性的纳米材料。我们的研究结果提供了有关具有不同性质的 MnO 纳米材料潜在有害影响的新见解,证明使用不同的人体体外模型进行危害评估是增加对其不同暴露途径潜在影响的知识的关键方面。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5736/9723098/0fcfefedb9de/41598_2022_25483_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5736/9723098/5164b950a529/41598_2022_25483_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5736/9723098/e48b00e147d9/41598_2022_25483_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5736/9723098/e2a21ca14e71/41598_2022_25483_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5736/9723098/8789c71663fe/41598_2022_25483_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5736/9723098/747055f282e7/41598_2022_25483_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5736/9723098/96dc1234a0c9/41598_2022_25483_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5736/9723098/93f53d06712d/41598_2022_25483_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5736/9723098/0fcfefedb9de/41598_2022_25483_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5736/9723098/5164b950a529/41598_2022_25483_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5736/9723098/e48b00e147d9/41598_2022_25483_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5736/9723098/e2a21ca14e71/41598_2022_25483_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5736/9723098/8789c71663fe/41598_2022_25483_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5736/9723098/747055f282e7/41598_2022_25483_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5736/9723098/96dc1234a0c9/41598_2022_25483_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5736/9723098/93f53d06712d/41598_2022_25483_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5736/9723098/0fcfefedb9de/41598_2022_25483_Fig8_HTML.jpg

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[4]
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[10]
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Drug Chem Toxicol. 2020-7

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