Tai Chien-Hsuan, Hsiung Suz-Kai, Chen Chih-Yuan, Tsai Mei-Lin, Lee Gwo-Bin
Department of Engineering Science, National Cheng Kung University, Tainan, Taiwan.
Biomed Microdevices. 2007 Aug;9(4):533-43. doi: 10.1007/s10544-007-9061-7.
This study reports a new biochip capable of cell separation and nucleus collection utilizing dielectrophoresis (DEP) forces in a microfluidic system comprising of micropumps and microvalves, operating in an automatic format. DEP forces operated at a low voltage (15 Vp-p) and at a specific frequency (16 MHz) can be used to separate cells in a continuous flow, which can be subsequently collected. In order to transport the cell samples continuously, a serpentine-shape (S-shape) pneumatic micropump device was constructed onto the chip device to drive the samples flow through the microchannel, which was activated by the pressurized air injection. The mixed cell samples were first injected into an inlet reservoir and driven through the DEP electrodes to separate specific samples. Finally, separated cell samples were collected individually in two outlet reservoirs controlled by microvalves. With the same operation principle, the nucleus of the specific cells can be collected after the cell lysis procedure. The pumping rate of the micropump was measured to be 39.8 microl/min at a pressure of 25 psi and a driving frequency of 28 Hz. For the cell separation process, the initial flow rate was 3 microl/min provided by the micropump. A throughput of 240 cells/min can be obtained by using the developed device. The DEP electrode array, microchannels, micropumps and microvalves are integrated on a microfluidic chip using micro-electro-mechanical-systems (MEMS) technology to perform several crucial procedures including cell transportation, separation and collection. The dimensions of the integrated chip device were measured to be 6x7 cm. By integrating an S-shape pump and pneumatic microvalves, different cells are automatically transported in the microchannel, separated by the DEP forces, and finally sorted to specific chambers. Experimental data show that viable and non-viable cells (human lung cancer cell, A549-luc-C8) can be successfully separated and collected using the developed microfluidic platform. The separation accuracy, depending on the DEP operating mode used, of the viable and non-viable cells are measured to be 84 and 81%, respectively. In addition, after cell lysis, the nucleus can be also collected using a similar scheme. The developed automatic microfluidic platform is useful for extracting nuclear proteins from living cells. The extracted nuclear proteins are ready for nuclear binding assays or the study of nuclear proteins.
本研究报告了一种新型生物芯片,该芯片能够在由微泵和微阀组成的微流控系统中利用介电泳(DEP)力进行细胞分离和细胞核收集,且以自动模式运行。在低电压(15 Vp-p)和特定频率(16 MHz)下运行的DEP力可用于在连续流中分离细胞,随后可对其进行收集。为了连续输送细胞样本,在芯片装置上构建了一个蛇形(S形)气动微泵装置,以驱动样本流过微通道,该装置由注入的压缩空气激活。混合细胞样本首先注入入口储液器,然后通过DEP电极以分离特定样本。最后,分离出的细胞样本分别收集到由微阀控制的两个出口储液器中。基于相同的操作原理,在细胞裂解程序后可收集特定细胞的细胞核。在25 psi的压力和28 Hz的驱动频率下,测得微泵的泵送速率为39.8微升/分钟。对于细胞分离过程,微泵提供的初始流速为3微升/分钟。使用所开发的装置可实现240个细胞/分钟的通量。DEP电极阵列、微通道、微泵和微阀采用微机电系统(MEMS)技术集成在微流控芯片上,以执行包括细胞运输、分离和收集在内的多个关键程序。所集成的芯片装置尺寸经测量为6×7厘米。通过集成S形泵和气动微阀,不同细胞在微通道中自动运输,通过DEP力分离,最终分选到特定腔室。实验数据表明,使用所开发的微流控平台能够成功分离并收集活细胞和死细胞(人肺癌细胞,A549-luc-C8)。根据所使用的DEP操作模式,活细胞和死细胞的分离准确率分别测得为84%和81%。此外,细胞裂解后,也可使用类似方案收集细胞核。所开发的自动微流控平台可用于从活细胞中提取核蛋白。提取的核蛋白可用于核结合测定或核蛋白研究。