Department of Chemistry, Imperial College London, Exhibition Road, South Kensington, London SW72AZ, UK.
Nat Chem. 2011 Jun;3(6):437-42. doi: 10.1038/nchem.1046.
Pipetting and dilution are universal processes used in chemical and biological laboratories to assay and experiment. In microfluidics such operations are equally in demand, but difficult to implement. Recently, droplet-based microfluidics has emerged as an exciting new platform for high-throughput experimentation. However, it is challenging to vary the concentration of droplets rapidly and controllably. To this end, we developed a dilution module for high-throughput screening using droplet-based microfluidics. Briefly, a nanolitre-sized sample droplet of defined concentration is trapped within a microfluidic chamber. Through a process of droplet merging, mixing and re-splitting, this droplet is combined with a series of smaller buffer droplets to generate a sequence of output droplets that define a digital concentration gradient. Importantly, the formed droplets can be merged with other reagent droplets to enable rapid chemical and biological screens. As a proof of concept, we used the dilutor to perform a high-throughput homogeneous DNA-binding assay using only nanolitres of sample.
移液和稀释是化学和生物实验室中用于分析和实验的通用过程。在微流控中,这些操作同样需要,但难以实现。最近,基于液滴的微流控技术已成为高通量实验的令人兴奋的新平台。然而,快速且可控地改变液滴的浓度具有挑战性。为此,我们开发了一种基于液滴的微流控高通量筛选用稀释模块。简而言之,将具有定义浓度的纳升级样品液滴捕获在微流控室中。通过液滴合并、混合和再分裂的过程,将该液滴与一系列较小的缓冲液滴组合,生成一系列定义数字浓度梯度的输出液滴。重要的是,形成的液滴可以与其他试剂液滴合并,以实现快速的化学和生物学筛选。作为概念验证,我们使用该稀释器仅使用纳升级的样品进行了高通量均相 DNA 结合分析。