Footz T, Wunsam S, Kulak S, Crabtree H J, Glerum D M, Backhouse C J
Department of Electrical and Computer Engineering, University of Alberta, Edmonton, Canada.
Electrophoresis. 2001 Oct;22(18):3868-75. doi: 10.1002/1522-2683(200110)22:18<3868::AID-ELPS3868>3.0.CO;2-F.
Sample preparation has long been recognized as a significant barrier to the implementation of macroscopic protocols on microfabricated devices. Macroscopically, such tasks as removing salts, primers and other contaminants are performed by methods involving precipitation, specialized membranes and centrifuges, none of which are readily performed in microfluidic structures. Although some microfluidic systems have been developed for performing sample purification, their complexity may hinder the degree to which they can be implemented. We present a method of microchip-based sample purification that can be performed with even the simplest microfluidic designs. The technique is demonstrated by removing primers from a sample of amplified DNA, leaving only the product DNA. This provides a new sample preparation capability for microfluidic systems.
长期以来,样品制备一直被认为是在微制造设备上实施宏观协议的重大障碍。在宏观层面上,诸如去除盐分、引物和其他污染物等任务是通过涉及沉淀、专用膜和离心机的方法来完成的,但这些方法在微流体结构中都不容易实现。尽管已经开发了一些用于样品纯化的微流体系统,但其复杂性可能会阻碍它们的实施程度。我们提出了一种基于微芯片的样品纯化方法,即使是最简单的微流体设计也能执行该方法。通过从扩增DNA样品中去除引物,仅留下产物DNA来证明该技术。这为微流体系统提供了一种新的样品制备能力。