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Sequential Cell-Processing System by Integrating Hydrodynamic Purification and Dielectrophoretic Trapping for Analyses of Suspended Cancer Cells

机译:流体动力学纯化和介电泳捕获相结合的顺序细胞处理系统用于悬浮癌细胞的分析

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摘要

Microfluidic devices employing dielectrophoresis (DEP) have been widely studied and applied in the manipulation and analysis of single cells. However, several pre-processing steps, such as the preparation of purified target samples and buffer exchanges, are necessary to utilize DEP forces for suspended cell samples. In this paper, a sequential cell-processing device, which is composed of pre-processing modules that employ deterministic lateral displacement (DLD) and a single-cell trapping device employing an electroactive microwell array (EMA), is proposed to perform the medium exchange followed by arraying single cells sequentially using DEP. Two original microfluidic devices were efficiently integrated by using the interconnecting substrate containing rubber gaskets that tightly connect the inlet and outlet of each device. Prostate cancer cells (PC3) suspended in phosphate-buffered saline buffer mixed with microbeads were separated and then resuspended into the DEP buffer in the integrated system. Thereafter, purified PC3 cells were trapped in a microwell array by using the positive DEP force. The achieved separation and trapping efficiencies exceeded 94% and 93%, respectively, when using the integrated processing system. This study demonstrates an integrated microfluidic device by processing suspended cell samples, without the requirement of complex preparation steps.
机译:使用介电泳(DEP)的微流体装置已被广泛研究,并应用于单细胞的操作和分析。但是,需要几个预处理步骤,例如纯化目标样品的制备和缓冲液交换,才能将DEP力用于悬浮细胞样品。本文提出了一种顺序细胞处理设备,该设备由采用确定性横向位移(DLD)的预处理模块和采用电活性微孔阵列(EMA)的单细胞捕获设备组成,以进行培养基交换然后依次使用DEP排列单个单元。通过使用包含橡胶垫圈的互连基板有效地集成了两个原始的微流体设备,该橡胶垫圈紧密连接每个设备的入口和出口。分离悬浮在磷酸盐缓冲液和微珠中的前列腺癌细胞(PC3),然后将其重新悬浮在集成系统的DEP缓冲液中。此后,通过使用正DEP力将纯化的PC3细胞捕获在微孔阵列中。使用集成处理系统时,分离效率和捕集效率分别超过94%和93%。这项研究证明了通过处理悬浮细胞样品而无需复杂制备步骤的集成微流体装置。

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