Department of Biomedical Engineering, College of Life Science and Technology, Huazhong University of Science and Technology, Wuhan 430074, China.
Biomed Microdevices. 2013 Jun;15(3):553-60. doi: 10.1007/s10544-013-9754-z.
Encapsulation of single cells is a challenging task in droplet microfluidics due to the random compartmentalization of cells dictated by Poisson statistics. In this paper, a microfluidic device was developed to improve the single-cell encapsulation rate by integrating droplet generation with fluorescence-activated droplet sorting. After cells were loaded into aqueous droplets by hydrodynamic focusing, an on-flight fluorescence-activated sorting process was conducted to isolate droplets containing one cell. Encapsulation of fluorescent polystyrene beads was investigated to evaluate the developed method. A single-bead encapsulation rate of more than 98 % was achieved under the optimized conditions. Application to encapsulate single HeLa cells was further demonstrated with a single-cell encapsulation rate of 94.1 %, which is about 200 % higher than those obtained by random compartmentalization. We expect this new method to provide a useful platform for encapsulating single cells, facilitating the development of high-throughput cell-based assays.
单细胞包封是液滴微流控中的一项挑战性任务,因为细胞的随机分隔由泊松统计决定。在本文中,开发了一种微流控设备,通过将液滴生成与荧光激活的液滴分选集成来提高单细胞包封率。细胞通过流体动力聚焦加载到水性液滴中后,进行飞行中的荧光激活分选过程,以分离含有一个细胞的液滴。研究了荧光聚苯乙烯珠的封装以评估所开发的方法。在优化条件下,实现了超过 98%的单珠封装率。进一步应用于封装单个 HeLa 细胞,单细胞封装率为 94.1%,比随机分隔法提高了约 200%。我们期望这种新方法为封装单个细胞提供一个有用的平台,促进高通量基于细胞的测定的发展。