Customizing droplet contents and dynamic ranges via integrated programmable picodroplet assembler

Pengfei Zhang; Aniruddha Kaushik; Kuangwen Hsieh; Tza-Huei Wang

doi:10.1038/s41378-019-0062-5

Customizing droplet contents and dynamic ranges via integrated programmable picodroplet assembler

Microsyst Nanoeng. 2019 Jul 1:5:22. doi: 10.1038/s41378-019-0062-5. eCollection 2019.

Authors

Pengfei Zhang^#¹, Aniruddha Kaushik^#², Kuangwen Hsieh^#², Tza-Huei Wang^{1

2}

Affiliations

¹ 1Department of Biomedical Engineering, Johns Hopkins University, 3400 N. Charles Street, Baltimore, MD 21218 USA.
² 2Department of Mechanical Engineering, Johns Hopkins University, 3400 N. Charles Street, Baltimore, MD 21218 USA.

^# Contributed equally.

Abstract

Droplet microfluidic technology is becoming increasingly useful for high-throughput and high-sensitivity detection of biological and biochemical reactions. Most current droplet devices function by passively discretizing a single sample subject to a homogeneous or random reagent/reaction condition into tens of thousands of picoliter-volume droplets for analysis. Despite their apparent advantages in speed and throughput, these droplet devices inherently lack the capability to customize the contents of droplets in order to test a single sample against multiple reagent conditions or multiple samples against multiple reagents. In order to incorporate such combinatorial capability into droplet platforms, we have developed the fully Integrated Programmable Picodroplet Assembler. Our platform is capable of generating customized picoliter-volume droplet groups from nanoliter-volume plugs which are assembled in situ on demand. By employing a combination of microvalves and flow-focusing-based discretization, our platform can be used to precisely control the content and volume of generated nanoliter-volume plugs, and thereafter the content and the effective dynamic range of picoliter-volume droplets. Furthermore, we can use a single integrated device for continuously generating, incubating, and detecting multiple distinct droplet groups. The device successfully marries the precise control and on-demand capability of microvalve-based platforms with the sensitivity and throughput of picoliter droplet platforms in a fully automated monolithic device. The device ultimately will find important applications in single-cell and single-molecule analyses.

Keywords: Engineering; Nanoscale devices.

Abstract

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