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本文引用的文献

1
Multiwalled carbon nanotubes induce a fibrogenic response by stimulating reactive oxygen species production, activating NF-κB signaling, and promoting fibroblast-to-myofibroblast transformation.多壁碳纳米管通过刺激活性氧的产生、激活 NF-κB 信号通路和促进成纤维细胞向肌成纤维细胞转化,引起纤维生成反应。
Chem Res Toxicol. 2011 Dec 19;24(12):2237-48. doi: 10.1021/tx200351d. Epub 2011 Nov 22.
2
Limitation of the MTT and XTT assays for measuring cell viability due to superoxide formation induced by nano-scale TiO2.由于纳米级 TiO2 诱导的超氧自由基的形成,MTT 和 XTT 测定法在测量细胞活力方面存在局限性。
Toxicol In Vitro. 2011 Dec;25(8):2147-51. doi: 10.1016/j.tiv.2011.07.007. Epub 2011 Jul 21.
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Cytotoxicity screening of single-walled carbon nanotubes: detection and removal of cytotoxic contaminants from carboxylated carbon nanotubes.单壁碳纳米管的细胞毒性筛选:羧基化碳纳米管中细胞毒性污染物的检测和去除。
Mol Pharm. 2011 Aug 1;8(4):1351-61. doi: 10.1021/mp2001439. Epub 2011 Jun 30.
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Role of oxidative stress and DNA damage in human carcinogenesis.氧化应激和 DNA 损伤在人类肿瘤发生中的作用。
Mutat Res. 2011 Jun 3;711(1-2):193-201. doi: 10.1016/j.mrfmmm.2010.12.016. Epub 2011 Jan 7.
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Implications of oxidative stress mechanisms in toxicity of nanoparticles (review).氧化应激机制在纳米颗粒毒性中的影响(综述)
Acta Physiol Hung. 2010 Sep;97(3):247-55. doi: 10.1556/APhysiol.97.2010.3.1.
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Cytotoxicity of multi-walled carbon nanotubes in three skin cellular models: effects of sonication, dispersive agents and corneous layer of reconstructed epidermis.多壁碳纳米管在三种皮肤细胞模型中的细胞毒性:超声处理、分散剂和重建表皮角质层的影响。
Nanotoxicology. 2010 Mar;4(1):84-97. doi: 10.3109/17435390903428869.
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A critical review of the biological mechanisms underlying the in vivo and in vitro toxicity of carbon nanotubes: The contribution of physico-chemical characteristics.碳纳米管体内和体外毒性的生物学机制的批判性综述:物理化学特性的贡献。
Nanotoxicology. 2010 Jun;4(2):207-46. doi: 10.3109/17435390903569639.
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Multi-walled carbon nanotubes induce cytotoxicity, genotoxicity and apoptosis in normal human dermal fibroblast cells.多壁碳纳米管可诱导正常人皮肤成纤维细胞产生细胞毒性、基因毒性并引发凋亡。
Ethn Dis. 2010 Winter;20(1 Suppl 1):S1-65-72.
9
Interfacing carbon nanotubes with living mammalian cells and cytotoxicity issues.将碳纳米管与活体哺乳动物细胞连接以及细胞毒性问题。
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Carbon nanotubes elicit DNA damage and inflammatory response relative to their size and shape.碳纳米管会因其大小和形状引发 DNA 损伤和炎症反应。
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具有羧基官能化的多壁碳纳米管对人皮肤角质形成细胞造成的DNA损伤。

DNA damage in human skin keratinocytes caused by multiwalled carbon nanotubes with carboxylate functionalization.

作者信息

McShan Danielle, Yu Hongtao

机构信息

Department of Chemistry and Biochemistry, Jackson State University, Jackson, MS, USA.

Department of Chemistry and Biochemistry, Jackson State University, Jackson, MS, USA

出版信息

Toxicol Ind Health. 2014 Jul;30(6):489-98. doi: 10.1177/0748233712459914. Epub 2012 Sep 25.

DOI:10.1177/0748233712459914
PMID:23012341
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3912206/
Abstract

Water-soluble carbon nanotubes have been found to be one of the most promising nanomaterials in biological- and biomedical-based applications. However, there have been major concerns on their ability to cause cellular and DNA damages upon exposure. In this work, we explore the toxic effects of three multiwalled carbon nanotubes (MWCNTs: nonpurified, purified and carboxylate-functionalized) on human skin keratinocytes (HaCaT). Cytotoxicity tests using the conventional thiazolyl blue tetrazolium bromide (MTT) and the water-soluble tetrazolium (WST-1) assays for 0.5 or 24 h exposure to 20 μg/mL of MWCNTs show that all three caused minimum cytotoxicity that is generally not statistically significant. Assessment of direct and oxidative DNA damages using both alkaline Comet assay and formamidopyrimidine DNA glycosylase-modified Comet assay reveals that the treatment with 20 μg/mL of MWCNTs does not cause significant direct DNA damages, but causes great amount of oxidative DNA damages in HaCaT cells. The oxidative DNA damage reaches the maximum amount at 4 h of incubation in Dulbecco's minimum essential medium, but decreases to the minimum at 8 and 24 h of incubation, indicating repair of the oxidative damages by the intrinsic DNA repair mechanism of the cells.

摘要

水溶性碳纳米管已被发现是生物和生物医学应用中最有前景的纳米材料之一。然而,人们对其暴露后导致细胞和DNA损伤的能力存在重大担忧。在这项工作中,我们研究了三种多壁碳纳米管(MWCNT:未纯化的、纯化的和羧基官能化的)对人皮肤角质形成细胞(HaCaT)的毒性作用。使用传统的噻唑蓝四唑溴盐(MTT)和水溶性四唑(WST-1)检测法,对暴露于20μg/mL MWCNT 0.5小时或24小时的细胞进行细胞毒性测试,结果表明,所有三种碳纳米管都引起了最小的细胞毒性,通常在统计学上不显著。使用碱性彗星试验和甲酰胺嘧啶DNA糖基化酶修饰的彗星试验评估直接和氧化性DNA损伤,结果显示,用20μg/mL MWCNT处理不会导致HaCaT细胞出现显著的直接DNA损伤,但会导致大量的氧化性DNA损伤。在杜尔贝科改良伊格尔培养基中孵育4小时时,氧化性DNA损伤达到最大量,但在孵育8小时和24小时时降至最低,这表明细胞的内在DNA修复机制修复了氧化性损伤。