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Investigation of the cytotoxicity mechanism of silver nanoparticles in vitro

机译:银纳米粒子体外细胞毒性机理的研究

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Nowadays, more and more nanotechnology products and nanomaterials are being applied in our lives. Silver nanoparticles (SNPs) are used in infection prevention and treatment due to their antimicrobial activity. However, as a kind of nanomaterial, the toxicology of SNPs has not been completely studied. The mechanism of cytotoxicity of SNPs in vitro to mouse's fibroblast cells (L929) was investigated in this study. As a contrast, silver microparticles (SMPs) were also studied. Propidium iodide (PI) single staining and Annexin-V/PI staining were carried out to unveil the influence of SNPs and SMPs on the cells. A transmission electron microscope (TEM) was used to observe SNPs' distribution in the cells. The results of cell cycle analysis indicated that the cells treated with SNPs were arrested in the G2M phase. Meanwhile, SNPs lead to apoptosis of more cells compared to SMPs at the same dose as a result of apoptosis analysis. Analysis of the cells' ultrastructure showed that SNPs could be phagocytized into the cells while SMPs could not. The mechanism of cytotoxicity of SNPs in vitro to L929 cells may be that SNPs are phagocytized into the cells and they interact with mitochondria or other organelles, even nuclei, which results in cells' apoptosis or necrosis.
机译:如今,越来越多的纳米技术产品和纳米材料正在我们的生活中应用。银纳米颗粒(SNP)由于其抗菌活性而被用于感染的预防和治疗。然而,作为一种纳米材料,单核苷酸多态性的毒理学尚未完全研究。在这项研究中,研究了SNPs对小鼠成纤维细胞(L929)的体外细胞毒性机制。作为对比,还研究了银微粒(SMP)。进行了碘化丙啶(PI)单一染色和膜联蛋白-V / PI染色以揭示SNP和SMP对细胞的影响。使用透射电子显微镜(TEM)观察SNP在细胞中的分布。细胞周期分析的结果表明,用SNPs处理的细胞被阻滞在G2M期。同时,由于凋亡分析,与相同剂量的SMP相比,SNP导致更多细胞的凋亡。对细胞超微结构的分析表明,SNPs可以被吞噬入细胞,而SMPs则不能。 SNP对L929细胞的体外细胞毒性作用机制可能是SNP被吞噬进入细胞,并且与线粒体或其他细胞器甚至细胞核相互作用,导致细胞凋亡或坏死。

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