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Materials and methods for droplet microfluidic device fabrication

Materials and methods for droplet microfluidic device fabrication
Materials and methods for droplet microfluidic device fabrication
Since the first reports two decades ago, droplet-based systems have emerged as a compelling tool for microbiological and (bio)chemical science, with droplet flow providing multiple advantages over standard single-phase microfluidics such as removal of Taylor dispersion, enhanced mixing, isolation of droplet contents from surfaces, and the ability to contain and address individual cells or biomolecules. Typically, a droplet microfluidic device is designed to produce droplets with well-defined sizes and compositions that flow through the device without interacting with channel walls. Successful droplet flow is fundamentally dependent on the microfluidic device – not only its geometry but moreover how the channel surfaces interact with the fluids. Here we summarise the materials and fabrication techniques required to make microfluidic devices that deliver controlled uniform droplet flow, looking not just at physical fabrication methods, but moreover how to select and modify surfaces to yield the required surface/fluid interactions. We describe the various materials, surface modification techniques, and channel geometry approaches that can be used, and give examples of the decision process when determining which material or method to use by describing the design process for five different devices with applications ranging from field-deployable chemical analysers to water-in-water droplet creation. Finally we consider how droplet microfluidic device fabrication is changing and will change in the future, and what challenges remain to be addressed in the field.
1473-0197
859-875
Nightingale, Adrian
4b51311d-c6c3-40d5-a13f-ab8917031ab3
Elvira, Katherine S.
a9eada3b-a5cc-4d4b-b741-ba54d882db21
Tsai, Scott
d3e05f2f-c34c-4f63-82f2-19dcc83456e1
Gielen, Fabrice
c77341af-6e84-468f-a89e-0dcda0a75139
Nightingale, Adrian
4b51311d-c6c3-40d5-a13f-ab8917031ab3
Elvira, Katherine S.
a9eada3b-a5cc-4d4b-b741-ba54d882db21
Tsai, Scott
d3e05f2f-c34c-4f63-82f2-19dcc83456e1
Gielen, Fabrice
c77341af-6e84-468f-a89e-0dcda0a75139

Nightingale, Adrian, Elvira, Katherine S., Tsai, Scott and Gielen, Fabrice (2022) Materials and methods for droplet microfluidic device fabrication. Lab on a Chip, 22 (5), 859-875. (doi:10.1039/d1lc00836f).

Record type: Review

Abstract

Since the first reports two decades ago, droplet-based systems have emerged as a compelling tool for microbiological and (bio)chemical science, with droplet flow providing multiple advantages over standard single-phase microfluidics such as removal of Taylor dispersion, enhanced mixing, isolation of droplet contents from surfaces, and the ability to contain and address individual cells or biomolecules. Typically, a droplet microfluidic device is designed to produce droplets with well-defined sizes and compositions that flow through the device without interacting with channel walls. Successful droplet flow is fundamentally dependent on the microfluidic device – not only its geometry but moreover how the channel surfaces interact with the fluids. Here we summarise the materials and fabrication techniques required to make microfluidic devices that deliver controlled uniform droplet flow, looking not just at physical fabrication methods, but moreover how to select and modify surfaces to yield the required surface/fluid interactions. We describe the various materials, surface modification techniques, and channel geometry approaches that can be used, and give examples of the decision process when determining which material or method to use by describing the design process for five different devices with applications ranging from field-deployable chemical analysers to water-in-water droplet creation. Finally we consider how droplet microfluidic device fabrication is changing and will change in the future, and what challenges remain to be addressed in the field.

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Accepted/In Press date: 21 January 2022
Published date: 7 March 2022
Additional Information: Funding Information: KSE's position is funded by the Canada Research Chairs program and the Michael Smith Foundation for Health Research in partnership with the Pacific Alzheimer Research Foundation. FG has received funding from the Biotechnology and Biological Sciences Research Council (grant BB/T011777/ 1) and the European Union's Horizon 2020 research and innovation programme (grant agreement No. 101000560). SSHT is thankful for support from the Government of Canada's Natural Sciences and Engineering Research Council (NSERC), Discovery Grants program (RGPIN-2019-04618). AMN is supported by the Natural Environment Research Council via an Industrial Innovation Fellowship (NE/R013578/1) and the Signals in the Soil program (NE/T010584/1). Publisher Copyright: © The Royal Society of Chemistry.

Identifiers

Local EPrints ID: 454519
URI: http://eprints.soton.ac.uk/id/eprint/454519
ISSN: 1473-0197
PURE UUID: a0d642a8-bb90-4e96-868a-0e612565d5a5
ORCID for Adrian Nightingale: ORCID iD orcid.org/0000-0003-2445-4827

Catalogue record

Date deposited: 15 Feb 2022 17:33
Last modified: 17 Mar 2024 07:05

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Contributors

Author: Katherine S. Elvira
Author: Scott Tsai
Author: Fabrice Gielen

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