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本文引用的文献

1
Hydroxylated fullerenes inhibit neutrophil function in fathead minnow (Pimephales promelas Rafinesque, 1820).羟基化富勒烯抑制黑头呆鱼(Pimephales promelas Rafinesque, 1820)中性粒细胞功能。
Aquat Toxicol. 2011 Jan 25;101(2):474-82. doi: 10.1016/j.aquatox.2010.11.002. Epub 2010 Nov 11.
2
Super-highly hydroxylated fullerene derivative protects human keratinocytes from UV-induced cell injuries together with the decreases in intracellular ROS generation and DNA damages.超高度羟基化富勒烯衍生物可减少细胞内 ROS 生成和 DNA 损伤,共同保护人角质形成细胞免受 UV 诱导的细胞损伤。
J Photochem Photobiol B. 2011 Jan 10;102(1):69-76. doi: 10.1016/j.jphotobiol.2010.09.006. Epub 2010 Oct 1.
3
Fullerenol C60(OH)24 prevents doxorubicin-induced acute cardiotoxicity in rats.富勒醇 C60(OH)24 可预防阿霉素诱导的大鼠急性心脏毒性。
Pharmacol Rep. 2010 Jul-Aug;62(4):707-18. doi: 10.1016/s1734-1140(10)70328-5.
4
Fullerenol cytotoxicity in kidney cells is associated with cytoskeleton disruption, autophagic vacuole accumulation, and mitochondrial dysfunction.富勒醇在肾细胞中的细胞毒性与细胞骨架破坏、自噬泡积累和线粒体功能障碍有关。
Toxicol Appl Pharmacol. 2010 Nov 1;248(3):249-58. doi: 10.1016/j.taap.2010.08.008. Epub 2010 Aug 14.
5
Intrinsic biological property of colloidal fullerene nanoparticles (nC60): lack of lethality after high dose exposure to human epidermal and bacterial cells.胶体富勒烯纳米粒子(nC60)的固有生物学特性:在高剂量暴露于人体表皮和细菌细胞后无致死性。
Toxicol Lett. 2010 Aug 16;197(2):128-34. doi: 10.1016/j.toxlet.2010.05.010. Epub 2010 May 21.
6
Effects of intracerebral microinjection of hydroxylated-[60]fullerene on brain monoamine concentrations and locomotor behavior in rats.脑室内微量注射羟基化-[60]富勒烯对大鼠脑单胺浓度及运动行为的影响。
J Nanosci Nanotechnol. 2010 Jan;10(1):604-11. doi: 10.1166/jnn.2010.1720.
7
Evaluation of silver nanoparticle toxicity in skin in vivo and keratinocytes in vitro.体内皮肤和体外角质细胞中纳米银颗粒毒性的评价。
Environ Health Perspect. 2010 Mar;118(3):407-13. doi: 10.1289/ehp.0901398. Epub 2009 Oct 23.
8
Interactions of aluminum nanoparticles with human epidermal keratinocytes.铝纳米颗粒与人表皮角质细胞的相互作用。
J Appl Toxicol. 2010 Apr;30(3):276-85. doi: 10.1002/jat.1494.
9
Biomedical applications of functionalized fullerene-based nanomaterials.基于功能化富勒烯纳米材料的生物医学应用。
Int J Nanomedicine. 2009;4:261-75.
10
Cellular uptake and cytotoxic evaluation of fullerenol in different cell lines.富勒醇在不同细胞系中的细胞摄取和细胞毒性评价。
Toxicology. 2010 Mar 10;269(2-3):155-9. doi: 10.1016/j.tox.2009.11.015. Epub 2009 Nov 24.

三种羟基化富勒烯在人皮肤细胞中的体外毒性评估。

In vitro toxicity assessment of three hydroxylated fullerenes in human skin cells.

机构信息

Center for Chemical Toxicology Research and Pharmacokinetics, North Carolina State University, Raleigh, NC 27607, USA.

出版信息

Toxicol In Vitro. 2011 Dec;25(8):2105-12. doi: 10.1016/j.tiv.2011.09.013. Epub 2011 Sep 22.

DOI:10.1016/j.tiv.2011.09.013
PMID:21964474
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3217115/
Abstract

Carbon fullerenes possess unique properties and their interactions with biomolecules have widespread applications. Functionalization of fullerenes with hydroxyl groups (fullerenols) can increase the solubility and potential for cellular interaction, but the health and safety effects of varying degrees of fullerene hydroxylation in biological systems is poorly understood. Existing reports regarding the toxicity and inflammatory potential of fullerenols give conflicting conclusions. To further elucidate the potential for toxicity of fullerenols, human epidermal keratinocytes (HEK) were exposed to fullerenols (low (C60(OH)20), medium (C60(OH)24), and high (C60(OH)32)) at concentrations ranging from 0.000544-42.5 μg/ml for 24 and 48 h. A statistically significant (p<0.05) decrease in viability with alamar Blue (aB) was noted only with C60(OH)32 at 42.5 μg/ml after 24 h. Nanoparticle (NP) controls showed minimal NP/assay interference of the three fullerenols with the aB viability assay. Normalized IL-8 concentration for C60(OH)20 was not significantly different from control, while C60(OH)24 and C60(OH)32 showed a significant decrease at 24 and 48 h. These results suggest that different hydroxylation of fullerenes caused no cytotoxicity or inflammation up to 8.55 μg/ml. These findings suggest that extrapolation across similar NP will be dependent upon surface chemistry and concentration which may affect the degree of agglomeration and thus biological effects.

摘要

碳富勒烯具有独特的性质,其与生物分子的相互作用具有广泛的应用。富勒烯的羟基化(富勒醇)可以增加其溶解度和与细胞相互作用的潜力,但生物系统中富勒烯不同程度羟基化的健康和安全影响还了解甚少。现有的关于富勒醇毒性和炎症潜力的报告得出了相互矛盾的结论。为了进一步阐明富勒醇的潜在毒性,将人表皮角质细胞(HEK)暴露于富勒醇(低(C60(OH)20)、中(C60(OH)24)和高(C60(OH)32))浓度范围为 0.000544-42.5μg/ml 24 和 48 小时。仅在用 C60(OH)32 处理 42.5μg/ml 24 小时后,alamar Blue(aB)检测到细胞活力的统计学显著(p<0.05)下降。纳米颗粒(NP)对照显示三种富勒醇的 NP/测定干扰极小,对 aB 活力测定无影响。与对照相比,C60(OH)20 的归一化 IL-8 浓度没有明显差异,而 C60(OH)24 和 C60(OH)32 在 24 和 48 小时显示出明显的降低。这些结果表明,富勒烯的不同羟基化在高达 8.55μg/ml 的浓度下不会引起细胞毒性或炎症。这些发现表明,跨类似 NP 的推断将取决于表面化学和浓度,这可能会影响团聚程度,从而影响生物效应。