Liu Yan-Jun, Guo Shi-Shang, Zhang Zhi-Ling, Huang Wei-Hua, Baigl Damien, Xie Min, Chen Yong, Pang Dai-Wen
College of Chemistry and Molecular Sciences, and State Key Laboratory of Virology, Wuhan University, Wuhan, PRC.
Electrophoresis. 2007 Dec;28(24):4713-22. doi: 10.1002/elps.200700212.
An integrated smart microfluidic device consisting of nickel micropillars, microvalves, and microchannels was developed for specific capture and sorting of cells. A regular hexagonal array of nickel micropillars was integrated on the bottom of a microchannel by standard photolithography, which can generate strong induced magnetic field gradients under an external magnetic field to efficiently trap superparamagnetic beads (SPMBs) in a flowing stream, forming a bed with sufficient magnetic beads as a capture zone. Fluids could be manipulated by programmed controlling the integrated air-pressure-actuated microvalves, based on which in situ bio-functionalization of SPMBs trapped in the capture zone was realized by covalent attachment of specific proteins directly to their surface on the integrated microfluidic device. In this case, only small volumes of protein solutions (62.5 nL in the capture zone; 375 nL in total volume needed to fill the device from inlet A to the intersection of outlet channels F and G) can meet the need for protein! The newly designed microfluidic device reduced greatly chemical and biological reagent consumption and simplified drastically tedious manual handling. Based on the specific interaction between wheat germ agglutinin (WGA) and N-acetylglucosamine on the cell membrane, A549 cancer cells were effectively captured and sorted on the microfluidic device. Capture efficiency ranged from 62 to 74%. The integrated microfluidic device provides a reliable technique for cell sorting.
一种由镍微柱、微阀和微通道组成的集成智能微流控装置被开发用于细胞的特异性捕获和分选。通过标准光刻技术在微通道底部集成了规则的六边形镍微柱阵列,在外部磁场作用下,该阵列能产生强大的感应磁场梯度,以有效地捕获流动流中的超顺磁性微珠(SPMBs),形成一个含有足够磁珠的床层作为捕获区。通过对集成的气压驱动微阀进行编程控制来操纵流体,基于此,通过将特定蛋白质直接共价连接到集成微流控装置中捕获区捕获的SPMBs表面,实现了SPMBs的原位生物功能化。在这种情况下,仅少量蛋白质溶液(捕获区为62.5 nL;从入口A到出口通道F和G的交叉点填充整个装置所需的总体积为375 nL)就能满足蛋白质需求!新设计的微流控装置大大减少了化学和生物试剂的消耗,并极大地简化了繁琐的手动操作。基于小麦胚芽凝集素(WGA)与细胞膜上N - 乙酰葡糖胺之间的特异性相互作用,在微流控装置上有效地捕获并分选了A549癌细胞。捕获效率在62%至74%之间。该集成微流控装置为细胞分选提供了一种可靠的技术。