Microfluidic on-demand droplet generation, storage, retrieval, and merging for single-cell pairing

被引:40
作者
Babahosseini, Hesam [1 ,2 ]
Misteli, Tom [1 ]
DeVoe, Don L. [2 ]
机构
[1] NCI, NIH, Bethesda, MD 20892 USA
[2] Univ Maryland, Dept Mech Engn, College Pk, MD 20742 USA
关键词
FLOW; ARRAY; FUSION; SYSTEM; DEVICE; ACTUATION; RELEASE; DESIGN; VOLUME;
D O I
10.1039/c8lc01178h
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A multifunctional microfluidic platform combining on-demand aqueous-phase droplet generation, multi-droplet storage, and controlled merging of droplets selected from a storage library in a single integrated microfluidic device is described. A unique aspect of the technology is a microfluidic trap design comprising a droplet trap chamber and lateral bypass channels integrated with a microvalve that supports the capture and merger of multiple droplets over a wide range of individual droplet sizes. A storage unit comprising an array of microfluidic traps operates in a first-in first-out manner, allowing droplets stored within the library to be analyzed before sequentially delivering selected droplets to a downstream merging zone, while shunting other droplets to waste. Performance of the microfluidic trap is investigated for variations in bypass/chamber hydrodynamic resistance ratio, micro-chamber geometry, trapped droplet volume, and overall flow rate. The integrated microfluidic platform is then utilized to demonstrate the operational steps necessary for cell-based assays requiring the isolation of defined cell populations with single cell resolution, including encapsulation of individual cells within an aqueous-phase droplet carrier, screening or incubation of the immobilized cell-encapsulated droplets, and generation of controlled combinations of individual cells through the sequential droplet merging process. Beyond its utility for cell analysis, the presented platform represents a versatile approach to robust droplet generation, storage, and merging for use in a wide range of droplet-based microfluidics applications.
引用
收藏
页码:493 / 502
页数:10
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