Lin Ling, Mawatari Kazuma, Morikawa Kyojiro, Kitamori Takehiko
Department of Bioengineering, School of Engineering, The University of Tokyo.
Anal Sci. 2016;32(1):75-8. doi: 10.2116/analsci.32.75.
Single cell analysis has been of great interest in recent years. In particular, to achieve living single cell analysis is the ultimate goal to study the dynamic process of the single cell. However, single cell volume is pL in scale, and it is difficult to realize living single cell analysis, even by microfluidic technology (nL-sub nL). Herein, a novel microfluidic platform was developed by integrating a single cell chamber and an extended-nano channel (aL-fL volume). A single cell was isolated and cultured for more than 12 h by pressure-driven flow control. In addition, an electric resistance measurement method was developed to monitor the cell viability without fluorescence labeling. This platform will provide a new method for living single cell analysis by utilizing the novel analytical functions of the extended-nano space.
近年来,单细胞分析备受关注。特别是,实现活细胞单细胞分析是研究单细胞动态过程的最终目标。然而,单细胞体积在皮升尺度,即使采用微流控技术(纳升至亚纳升)也难以实现活细胞单细胞分析。在此,通过整合单细胞腔室和扩展纳米通道(阿托升至飞升级体积)开发了一种新型微流控平台。通过压力驱动的流量控制分离并培养单个细胞超过12小时。此外,还开发了一种电阻测量方法,无需荧光标记即可监测细胞活力。该平台将利用扩展纳米空间的新型分析功能为活细胞单细胞分析提供一种新方法。