Department of Mechanical and Aerospace Engineering, Monash University, Clayton, VIC 3800, Australia.
Lab Chip. 2017 Jul 11;17(14):2372-2394. doi: 10.1039/c7lc00005g.
The transition from micro well plate and robotics based high throughput screening (HTS) to chip based screening has already started. This transition promises reduced droplet volumes thereby decreasing the amount of fluids used in these studies. Moreover, it significantly boosts throughput allowing screening to keep pace with the overwhelming number of molecular targets being discovered. In this review, we analyse state-of-the-art droplet control technologies that exhibit potential to be used in this new generation of screening devices. Since these systems are enclosed and usually planar, even some of the straightforward methods used in traditional HTS such as pipetting and reading can prove challenging to replicate in microfluidic high throughput screening (μHTS). We critically review the technologies developed for this purpose in depth, describing the underlying physics and discussing the future outlooks.
从微孔板和基于机器人的高通量筛选(HTS)向基于芯片的筛选的转变已经开始。这种转变有望减少液滴体积,从而减少这些研究中使用的液体量。此外,它还显著提高了通量,使筛选能够跟上大量新发现的分子靶标。在这篇综述中,我们分析了最先进的液滴控制技术,这些技术有可能用于新一代筛选设备。由于这些系统是封闭的,通常是平面的,即使是在传统 HTS 中使用的一些简单方法,如移液和读取,在微流控高通量筛选(μHTS)中也可能难以复制。我们深入地批判性地回顾了为此目的开发的技术,描述了基础物理学,并讨论了未来的前景。