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Compare Analysis for the Nanotoxicity Effects of Different Amounts of Endocytic Iron Oxide Nanoparticles at Single Cell Level

机译:在单细胞水平上比较不同量的内吞氧化铁纳米颗粒的纳米毒性效应的比较分析

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摘要

Developing methods that evaluate the cellular uptake of magnetic nanoparticles (MNPs) and nanotoxicity effects at single-cellular level are needed. In this study, magnetophoresis combining fluorescence based cytotoxicity assay was proposed to assess the viability and the single-cellular MNPs uptake simultaneously. Malignant cells (SKHep-1, HepG2, HeLa) were incubated with 10 nm anionic iron oxide nanoparticles. Prussian blue stain was performed to visualize the distribution of magnetic nanoparticles. MTT and fluorescence based assay analyzed the cytotoxicity effects of the bulk cell population and single cell, respectively. DAPI/PI stained was applied to evaluate death mechanism. The number of intracellular MNPs was found to be strongly correlated with the cell death. Significant differences between cellular MNP uptake in living and dead cells were observed. The method could be useful for future study of the nanotoxicity induced by MNPs.
机译:需要开发方法来评估磁性纳米颗粒(MNP)的细胞吸收以及单细胞水平的纳米毒性作用。在这项研究中,磁泳结合基于荧光的细胞毒性测定法被提出来评估生存力和同时摄取单细胞MNPs。将恶性细胞(SKHep-1,HepG2,HeLa)与10 nm阴离子氧化铁纳米颗粒孵育。进行普鲁士蓝染色以可视化磁性纳米颗粒的分布。 MTT和基于荧光的分析分别分析了大细胞群和单细胞的细胞毒性作用。 DAPI / PI染色用于评估死亡机制。发现细胞内MNP的数量与细胞死亡强烈相关。观察到活细胞和死细胞中细胞MNP摄取之间的显着差异。该方法可用于未来研究由MNPs诱导的纳米毒性。

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