LIMMS-CNRS/IIS, Institute of Industrial Science, University of Tokyo, Tokyo, Japan.
Electrophoresis. 2010 Nov;31(22):3719-26. doi: 10.1002/elps.201000295. Epub 2010 Oct 22.
Sequential operations of pre-separation reaction process by picoliter droplets and following electrophoretic separation process were realized in a single microfluidic device with pneumatic handling of liquid. The developed device consists of a fluidic chip made of PDMS, an electrode substrate, and a temperature control substrate on which thin film heater/sensor structures are fabricated. Liquid handling, including introduction of liquid samples, droplet generation, and merging of droplets, was implemented by pneumatic manipulation through microcapillary vent structures, allowing air to pass and stop liquid flow. Since the pneumatic manipulations are conducted in a fully automated manner by using a programmable air pressure control system, the user simply has to load liquid samples on each liquid port of the device. Droplets of 420 pL were generated with an accuracy of ± 2 pL by applying droplet generation pressure in the range of 40-100 kPa. As a demonstration, a binding reaction of a 15 mer ssDNA with a peptide nucleic acid oligomer used as an oligoprobe followed by denaturing electrophoresis to discriminate a single-base substitution was performed within 1.5 min. By exploiting the droplet-on-demand capability of the device, the influence of various factors, such as reaction time, mixing ratio and droplet configurations on the ssDNA-peptide nucleic acid binding reaction in the droplet-based process, was studied toward realization of a rapid detection method to discriminate rapid single-base substitution.
通过皮升液滴的预分离反应过程的顺序操作和随后的电泳分离过程在单个微流控装置中实现,该装置采用气动处理液体。该开发的装置由 PDMS 制成的流道芯片、电极基板和温度控制基板组成,在薄膜加热器/传感器结构上制造。包括引入液体样品、液滴生成和液滴合并在内的液体处理通过微毛细管通风结构的气动操作来实现,允许空气通过并停止液体流动。由于气动操作通过使用可编程气压控制系统以全自动方式进行,因此用户只需在设备的每个液体端口上加载液体样品。通过在 40-100 kPa 的范围内施加液滴生成压力,可生成精度为±2 pL 的 420 pL 液滴。作为演示,在 1.5 分钟内完成了 15 个 ssDNA 与用作寡探针的肽核酸寡聚物的结合反应,随后进行变性电泳以区分单个碱基取代。通过利用该设备的按需液滴功能,研究了各种因素,例如反应时间、混合比和液滴配置对基于液滴的过程中 ssDNA-肽核酸结合反应的影响,以实现快速检测方法来区分快速单碱基取代。