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Cytotoxicity of cadmium-containing quantum dots based on a study using a microfluidic chip

机译:基于微流控芯片研究的含镉量子点的细胞毒性

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There is a lack of reliable nanotoxicity assays available for monitoring and quantifying multiple cellular events in cultured cells. In this study, we used a microfluidic chip to systematically investigate the cytotoxicity of three kinds of well-characterized cadmium-containing quantum dots (QDs) with the same core but different shell structures, including CdTe core QDs, CdTe/CdS coreshell QDs, and CdTe/CdS/ZnS coreshellshell QDs, in HEK293 cells. Using the microfluidic chip combined with fluorescence microscopy, multiple QD-induced cellular events including cell morphology, viability, proliferation, and QD uptake were simultaneously analysed. The three kinds of QDs showed significantly different cytotoxicities. The CdTe QDs, which are highly toxic to HEK293 cells, resulted in remarkable cellular and nuclear morphological changes, a dose-dependent decrease in cell viability, and strong inhibition of cell proliferation; the CdTe/CdS QDs were moderately toxic but did not significantly affect the proliferation of HEK293 cells; while the CdTe/CdS/ZnS QDs had no detectable influence on cytotoxicity with respect to cell morphology, viability, and proliferation. Our data indicated that QD cytotoxicity was closely related to their surface structures and specific physicochemical properties. This study also demonstrated that the microfluidic chip could serve as a powerful tool to systematically evaluate the cytotoxicity of nanoparticles in multiple cellular events.
机译:缺乏可用于监测和定量培养细胞中多个细胞事件的可靠的纳米毒性测定法。在这项研究中,我们使用微流控芯片系统地研究了三种具有相同核心但壳结构不同的,表征良好的含镉量子点(QD)的细胞毒性,包括CdTe核心QD,CdTe / CdS核心壳QD和HEK293细胞中的CdTe / CdS / ZnS核壳QD。使用结合荧光显微镜的微流控芯片,可以同时分析多个QD诱导的细胞事件,包括细胞形态,活力,增殖和QD摄取。三种量子点显示出明显不同的细胞毒性。对HEK293细胞具有高毒性的CdTe量子点导致细胞和核形态发生显着变化,细胞活力呈剂量依赖性下降,并强烈抑制细胞增殖。 CdTe / CdS QDs具有中等毒性,但对HEK293细胞的增殖没有明显影响。而CdTe / CdS / ZnS量子点对细胞形态,活力和增殖的细胞毒性没有可检测的影响。我们的数据表明QD的细胞毒性与其表面结构和特定的理化特性密切相关。这项研究还表明,微流控芯片可以作为系统评估纳米颗粒在多种细胞事件中的细胞毒性的有力工具。

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