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


Journal

Lab on a chip
ISSN: 1473-0189
Titre abrégé: Lab Chip
Pays: England
ID NLM: 101128948

Informations de publication

Date de publication:
29 01 2019
Historique:
pubmed: 10 1 2019
medline: 14 8 2019
entrez: 10 1 2019
Statut: ppublish

Résumé

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.

Identifiants

pubmed: 30623951
doi: 10.1039/c8lc01178h
pmc: PMC6692136
mid: NIHMS1041491
doi:

Types de publication

Journal Article

Langues

eng

Pagination

493-502

Subventions

Organisme : Intramural NIH HHS
ID : ZIA BC010309-19
Pays : United States
Organisme : Intramural NIH HHS
ID : ZIA BC010309-20
Pays : United States

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Auteurs

Hesam Babahosseini (H)

National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA and Department of Mechanical Engineering, University of Maryland, College Park, MD, 20742 USA. ddev@umd.edu.

Tom Misteli (T)

National Cancer Institute, National Institutes of Health, Bethesda, MD 20892, USA.

Don L DeVoe (DL)

Department of Mechanical Engineering, University of Maryland, College Park, MD, 20742 USA. ddev@umd.edu.

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