Okura Naoaki, Nakashoji Yuta, Koshirogane Toshihiro, Kondo Masaki, Tanaka Yugo, Inoue Kohei, Hashimoto Masahiko
Department of Chemical Engineering and Materials Science, Faculty of Science and Engineering, Doshisha University, Kyotanabe, Kyoto, Japan.
Electrophoresis. 2017 Oct;38(20):2666-2672. doi: 10.1002/elps.201700039. Epub 2017 Jul 24.
We have exploited a compact and facile microfluidic droplet creation device consisting of a poly(dimethylsiloxane) microfluidic chip possessing T-junction channel geometry, two inlet reservoirs, and one outlet reservoir, and a piezoelectric (PZT) diaphragm micropump with controller. Air was evacuated from the outlet reservoir using the PZT pump, reducing the pressure inside. The reduced pressure within the outlet reservoir pulled oil and aqueous solution preloaded in the inlet reservoirs into the microchannels, which then merged at the T-junction, successfully forming water-in-oil emulsion droplets at a rate of ∼1000 per second with minimal sample loss. We confirmed that the onset of droplet formation occurred immediately after turning on the pump (<1 s). Over repeated runs, droplet formation was highly reproducible, with droplet size purity (polydispersity, <4%) comparable to that achieved using other microfluidic droplet preparation techniques. We also demonstrated single-molecule PCR amplification in the created droplets, suggesting that the device could be used for effective droplet digital PCR platforms in most laboratories without requiring great expense, space, or time for acquiring technical skills.
我们开发了一种紧凑且简便的微流控液滴生成装置,该装置由一个具有T型通道几何结构的聚二甲基硅氧烷微流控芯片、两个入口储液器、一个出口储液器以及一个带控制器的压电(PZT)隔膜微泵组成。使用PZT泵从出口储液器中抽出空气,降低其内部压力。出口储液器内降低的压力将预加载在入口储液器中的油和水溶液吸入微通道,然后它们在T型连接处合并,以每秒约1000个的速率成功形成油包水乳液液滴,且样品损失极小。我们证实,打开泵后立即(<1秒)就开始形成液滴。在多次重复运行中,液滴形成具有高度可重复性,液滴尺寸纯度(多分散性,<4%)与使用其他微流控液滴制备技术所达到的纯度相当。我们还在生成的液滴中展示了单分子PCR扩增,这表明该装置可用于大多数实验室的高效液滴数字PCR平台,而无需花费大量资金、空间或时间来获取技术技能。