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首页> 外文期刊>Electrophoresis: The Official Journal of the International Electrophoresis Society >The potential of autofluorescence for the detection of single living cells for label-free cell sorting in microfluidic systems.
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The potential of autofluorescence for the detection of single living cells for label-free cell sorting in microfluidic systems.

机译:自体荧光检测微流体系统中无标记细胞分选的单个活细胞的潜力。

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摘要

A novel method for studying unlabeled living mammalian cells based on their autofluorescence (AF) signal in a prototype microfluidic device is presented. When combined, cellular AF detection and microfluidic devices have the potential to facilitate high-throughput analysis of different cell populations. To demonstrate this, unlabeled cultured cells in microfluidic devices were excited with a 488 nm excitation light and the AF emission (> 505 nm) was detected using a confocal fluorescence microscope (CFM). For example, a simple microfluidic three-port glass microstructure was used together with conventional electroosmotic flow (EOF) to switch the direction of the fluid flow. As a means to test the potential of AF-based cell sorting in this microfluidic device, granulocytes were successfully differentiated from human red blood cells (RBCs) based on differences in AF. This study demonstrated the use of a simple microfabricated device to perform high-throughput live cell detection and differentiation without the need for cell-specific fluorescent labeling dyes and thereby reducing the sample preparation time. Hence, the combined use of microfluidic devices and cell AF may have many applications in single-cell analysis.
机译:提出了一种新的方法,用于研究原型微流控设备中基于自身荧光(AF)信号的未标记活体哺乳动物细胞。结合使用时,细胞房颤检测和微流控设备具有促进不同细胞群体高通量分析的潜力。为了证明这一点,微流体设备中未标记的培养细胞用488 nm激发光激发,并使用共聚焦荧光显微镜(CFM)检测AF发射(> 505 nm)。例如,将简单的微流体三端口玻璃微结构与常规电渗流(EOF)一起使用以切换流体流动的方向。作为测试该微流体设备中基于AF的细胞分类潜力的一种手段,粒细胞已根据AF的差异成功地与人类红细胞(RBC)区别开来。这项研究表明,使用简单的微细加工设备即可进行高通量活细胞检测和分化,而无需使用细胞特异性荧光标记染料,从而减少了样品制备时间。因此,微流控设备和细胞房颤的组合使用可能在单细胞分析中有许多应用。

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