Department of Mechanical and Mechatronics Engineering, University of Waterloo, Waterloo, ON, Canada.
Electrophoresis. 2010 Mar;31(5):868-78. doi: 10.1002/elps.200900447.
A major challenge in lab-on-a-chip devices is how to concentrate sample molecules from a dilute solution, which is critical to the effectiveness and the detection limit of on-chip bio-chemical reactions. A numerical study of sample concentration control by electrokinetic microfluidic means in a closed-end microchannel is presented in this paper. The present method provides a simple and efficient way of concentration control by using electrokinetic trapping of a charged species of interest, controlling liquid flow and separating different sample molecules in the microchannel. The electrokinetic-concentration process and the controlled transport of the sample molecules are numerically studied. In this system, in addition to the electroosmotic flow and the electrophoresis, the closed-end of the chamber causes velocity variation at both ends of the channel and induces a pressure gradient and the associated fluid movement in the channel. The combined effects determine the final concentration field of the sample molecules. The influences of a number of parameters such as the channel dimensions, electrode size and the applied electric field are investigated.
在微流控芯片设备中,一个主要的挑战是如何从稀释溶液中浓缩样品分子,这对于芯片上生化反应的有效性和检测极限至关重要。本文提出了一种在封闭微通道中用电动力学微流控手段控制样品浓缩的数值研究。本方法通过电动力学捕获感兴趣的带电物质、控制液体流动以及在微通道中分离不同的样品分子,提供了一种简单高效的浓度控制方法。本文对电动力学浓缩过程和样品分子的受控输运进行了数值研究。在该系统中,除了电渗流和电泳之外,腔室的封闭端导致通道两端的速度变化,并在通道中诱导压力梯度和相关的流体运动。这些组合效应决定了样品分子的最终浓度场。研究了通道尺寸、电极尺寸和外加电场等多个参数的影响。