Fiedler S, Shirley S G, Schnelle T, Fuhr G
Institut für Biologie-Membranphysiologie, Humboldt Universität zu Berlin, FRG.
Anal Chem. 1998 May 1;70(9):1909-15. doi: 10.1021/ac971063b.
There are highly sensitive analytical techniques for probing cellular and molecular events in very small volumes. The development of microtools for effective sample handling and separation in such volumes remains a challenge. Most devices developed so far use electrophoretic and chromatographic separation methods. We show that forces generated by ac fields under conditions of negative dielectrophoresis (DEP) can also be used. Miniaturized electrode arrays are housed in a microchannel and driven with high-frequency ac. A laminar liquid flow carries particles past the electrodes. Modification of the ac drive changes the particle trajectories. We have handled latex particles of micrometer size and living mammalian cells in a device which consists of the following four elements: a planar funnel which concentrates particles from a 1-mm-wide stream to a beam of about 50-micron width, an aligner which narrows the beam further and acts to break up particle aggregates, a field cage which can be used to trap particles, and a switch which can direct particles into one of two output channels. The electrodes are made from platinum/titanium and indium tin oxide (ITO) on glass substrates. Particle concentration and switching could be achieved for linear flow velocities up to about 10 mm s-1. The combination of this new method with high-performance optical detection offers prospects for miniaturized flow cytometry.
存在用于探测极微小体积内细胞和分子事件的高灵敏度分析技术。开发用于在此类体积中有效进行样品处理和分离的微工具仍然是一项挑战。迄今为止开发的大多数设备都采用电泳和色谱分离方法。我们表明,在负介电泳(DEP)条件下交流电场产生的力也可加以利用。小型化电极阵列置于微通道中,并由高频交流电驱动。层流携带颗粒经过电极。改变交流驱动会改变颗粒轨迹。我们在一种由以下四个元件组成的设备中处理了微米级大小的乳胶颗粒和活的哺乳动物细胞:一个平面漏斗,将颗粒从1毫米宽的流中浓缩到约50微米宽的束流;一个对准器,进一步使束流变窄并用于打散颗粒聚集体;一个场笼,可用于捕获颗粒;以及一个开关,可将颗粒引导至两个输出通道之一。电极由玻璃基板上的铂/钛和氧化铟锡(ITO)制成。对于高达约10毫米/秒的线性流速,可实现颗粒浓缩和切换。这种新方法与高性能光学检测相结合,为小型化流式细胞术带来了前景。