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通过集成双孔阵列微流控装置在单细胞水平对细胞内物质进行荧光定量分析。

Fluorescence quantification of intracellular materials at the single-cell level by an integrated dual-well array microfluidic device.

机构信息

State Key Laboratory on Integrated Optoelectronics, Institute of Semiconductors, Chinese Academy of Sciences, Beijing 100083, China.

出版信息

Analyst. 2019 Apr 8;144(8):2811-2819. doi: 10.1039/c9an00153k.

Abstract

We present an integrated microfluidic device for quantifying intracellular materials at the single-cell level. This device combines a dual-well structure and a microfluidic control system. The dual-well structure includes capture wells (20 μm in diameter) for trapping a single cell and reaction wells (200 μm in diameter) for confining reagents. The control system enables a programmable procedure for single-cell analysis. This device achieves highly efficient trapping of single cells, overcoming the Poisson distribution, while affording sufficient biochemical reagents for each isolated reactor. We successfully utilized the presented device to monitor the catalytic interaction between intracellular alkaline phosphatase enzyme and a fluorogenic substrate and to quantify the intracellular glucose concentration of a single K562 cell based on an external standard method. The results demonstrate the feasibility and convenience of our dual-well array microfluidic device as a practical single-cell research tool.

摘要

我们提出了一种用于在单细胞水平上定量细胞内物质的集成微流控装置。该装置结合了双井结构和微流控控制系统。双井结构包括用于捕获单个细胞的捕获井(直径 20μm)和用于容纳试剂的反应井(直径 200μm)。控制系统能够实现可编程的单细胞分析程序。该装置实现了高效捕获单细胞,克服了泊松分布,同时为每个隔离的反应器提供了足够的生化试剂。我们成功地利用该装置监测了细胞内碱性磷酸酶酶与荧光底物之间的催化相互作用,并基于外部标准方法对单个 K562 细胞内的葡萄糖浓度进行定量。结果表明,我们的双井阵列微流控装置作为一种实用的单细胞研究工具具有可行性和便利性。

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