- Isozaki, A;
- Nakagawa, Y;
- Loo, MH;
- Shibata, Y;
- Tanaka, N;
- Setyaningrum, DL;
- Park, J-W;
- Shirasaki, Y;
- Mikami, H;
- Huang, D;
- Tsoi, H;
- Riche, CT;
- Ota, T;
- Miwa, H;
- Kanda, Y;
- Ito, T;
- Yamada, K;
- Iwata, O;
- Suzuki, K;
- Ohnuki, S;
- Ohya, Y;
- Kato, Y;
- Hasunuma, T;
- Matsusaka, S;
- Yamagishi, M;
- Yazawa, M;
- Uemura, S;
- Nagasawa, K;
- Watarai, H;
- Di Carlo, D;
- Goda, K
Droplet microfluidics has become a powerful tool in precision medicine, green biotechnology, and cell therapy for single-cell analysis and selection by virtue of its ability to effectively confine cells. However, there remains a fundamental trade-off between droplet volume and sorting throughput, limiting the advantages of droplet microfluidics to small droplets (<10 pl) that are incompatible with long-term maintenance and growth of most cells. We present a sequentially addressable dielectrophoretic array (SADA) sorter to overcome this problem. The SADA sorter uses an on-chip array of electrodes activated and deactivated in a sequence synchronized to the speed and position of a passing target droplet to deliver an accumulated dielectrophoretic force and gently pull it in the direction of sorting in a high-speed flow. We use it to demonstrate large-droplet sorting with ~20-fold higher throughputs than conventional techniques and apply it to long-term single-cell analysis of Saccharomyces cerevisiae based on their growth rate.