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High-throughput sorting of nanoliter droplets enabled by a sequentially addressable dielectrophoretic array
Authors:Mun Hong Loo  Yuta Nakagawa  Soo Hyeon Kim  Akihiro Isozaki  Keisuke Goda
Institution:1. Department of Chemistry, The University of Tokyo, Tokyo, Japan

Mun Hong Loo and Yuta Nakagawa contributed equally to this paper.;2. Department of Chemistry, The University of Tokyo, Tokyo, Japan;3. Institute of Industrial Science, The University of Tokyo, Tokyo, Japan

Abstract:Droplet microfluidics has emerged as a powerful tool for a diverse range of biomedical and industrial applications such as single-cell analysis, directed evolution, and metabolic engineering. In these applications, droplet sorting has been effective for isolating small droplets encapsulating molecules, cells, or crystals of interest. Recently, there is an increased interest in extending the applicability of droplet sorting to larger droplets to utilize their size advantage. However, sorting throughputs of large droplets have been limited, hampering their wide adoption. Here, we report our demonstration of high-throughput fluorescence-activated droplet sorting of 1 nL droplets using an upgraded version of the sequentially addressable dielectrophoretic array (SADA), which we reported previously. The SADA is an array of electrodes that are individually and sequentially activated/deactivated according to the speed and position of a droplet passing nearby the array. We upgraded the SADA by increasing the number of driving electrodes constituting the SADA and incorporating a slanted microchannel. By using a ten-electrode SADA with the slanted microchannel, we achieved fluorescence-activated droplet sorting of 1 nL droplets at a record high throughput of 1752 droplets/s, twice as high as the previously reported maximum sorting throughput of 1 nL droplets.
Keywords:Dielectrophoresis  Droplet microfluidics  Droplet sorting  Microfluidics  Single-cell analysis
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