Laboratoire de Structure et Dynamique par Résonance Magnétique, CEA-CNRS UMR3299 SIS2M, IRAMIS, CEA Saclay, bât 639 pce 10, 91191 Gif sur Yvette, France.
Toxicol Lett. 2010 Oct 20;198(3):324-30. doi: 10.1016/j.toxlet.2010.07.009. Epub 2010 Jul 23.
Silicon carbide (SiC) is considered a highly biocompatible material, consequently SiC nanoparticles (NPs) have been proposed for potential applications in diverse areas of technology. Since no toxicological data are available for these NPs, the aim of this study was to draw their global toxicological profile on A549 lung epithelial cells, using a battery of classical in vitro assays. Five SiC-NPs, with varying diameters and Si/C ratios were used, and we show that these SiC-NPs are internalized in cells where they cause a significant, though limited, cytotoxic effect. Cell redox status is deeply disturbed: SiC-NP exposure cause reactive oxygen species production, glutathione depletion and inactivation of some antioxidant enzymes: glutathione reductase, superoxide dismutase, but not catalase. Finally, the alkaline comet assay shows that SiC-NPs are genotoxic. Taken together, these data prove that SiC-NPs biocompatibility should be revisited.
碳化硅(SiC)被认为是一种高度生物相容的材料,因此碳化硅纳米颗粒(NPs)已被提议用于技术的各个领域的潜在应用。由于这些 NPs 没有毒理学数据,因此本研究旨在使用一系列经典的体外检测方法,研究它们对 A549 肺上皮细胞的全面毒理学特征。使用了五种具有不同直径和 Si/C 比的 SiC-NPs,我们表明这些 SiC-NPs 被细胞内化,导致明显但有限的细胞毒性作用。细胞氧化还原状态受到严重干扰:SiC-NP 暴露会导致活性氧的产生、谷胱甘肽的消耗和一些抗氧化酶的失活:谷胱甘肽还原酶、超氧化物歧化酶,但不是过氧化氢酶。最后,碱性彗星试验表明 SiC-NPs 具有遗传毒性。总之,这些数据证明 SiC-NPs 的生物相容性需要重新评估。