Sasaki Naoki, Sugenami Eisuke
Department of Applied Chemistry, Faculty of Science and Engineering, Toyo University, 2100 Kujirai, Kawagoe, Saitama 350-8585, Japan.
Department of Chemistry, College of Science, Rikkyo University, 3-34-1 Nishi-Ikebukuro, Toshima, Tokyo 171-8501, Japan.
Micromachines (Basel). 2021 Feb 5;12(2):160. doi: 10.3390/mi12020160.
The use of micrometer-sized droplets for chemical and biochemical analysis has been widely explored. Photolithography is mainly used to fabricate microfluidic devices, which is often employed to form monodisperse microdroplets. Although photolithography enables precise microfabrication, it is not readily available to biochemists because it requires specialized equipment such as clean room and mask aligners, and expensive consumables such as photoresist and silicon wafers. In this study, we fabricated a microfluidic device using a consumer laser cutter and applied it to droplet formation. Monodisperse microdroplets were formed by using an oil phase for droplet digital polymerase chain reaction (PCR) as the continuous phase and phosphate-buffered saline or polyethylene glycol solution as the dispersed phase. The droplet size decreased as the flow rate of the continuous phase increased and approached a constant value. The method developed in this study can be used to realize microdroplet-based biochemical analysis with simple devices or to construct artificial cells.
微米级液滴在化学和生化分析中的应用已得到广泛探索。光刻技术主要用于制造微流控装置,该装置常被用于形成单分散微滴。尽管光刻技术能够实现精确的微制造,但生物化学家难以轻易使用,因为它需要洁净室和掩膜对准器等专业设备,以及光刻胶和硅片等昂贵耗材。在本研究中,我们使用消费级激光切割机制造了一种微流控装置,并将其应用于液滴形成。通过将用于液滴数字聚合酶链反应(PCR)的油相作为连续相,磷酸盐缓冲盐水或聚乙二醇溶液作为分散相,形成了单分散微滴。随着连续相流速的增加,液滴尺寸减小并趋于恒定值。本研究中开发的方法可用于通过简单装置实现基于微滴的生化分析或构建人工细胞。