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Microfluidic Chamber Design for Controlled Droplet Expansion and Coalescence
The defined formation and expansion of droplets are essential operations for droplet-based screening assays. The volumetric expansion of droplets causes a dilution of the ingredients. Dilution is required for the generation of concentration graduation which is mandatory for many different assay prot...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7231328/ https://www.ncbi.nlm.nih.gov/pubmed/32290165 http://dx.doi.org/10.3390/mi11040394 |
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author | Kielpinski, Mark Walther, Oliver Cao, Jialan Henkel, Thomas Köhler, J. Michael Groß, G. Alexander |
author_facet | Kielpinski, Mark Walther, Oliver Cao, Jialan Henkel, Thomas Köhler, J. Michael Groß, G. Alexander |
author_sort | Kielpinski, Mark |
collection | PubMed |
description | The defined formation and expansion of droplets are essential operations for droplet-based screening assays. The volumetric expansion of droplets causes a dilution of the ingredients. Dilution is required for the generation of concentration graduation which is mandatory for many different assay protocols. Here, we describe the design of a microfluidic operation unit based on a bypassed chamber and its operation modes. The different operation modes enable the defined formation of sub-µL droplets on the one hand and the expansion of low nL to sub-µL droplets by controlled coalescence on the other. In this way the chamber acts as fluidic interface between two fluidic network parts dimensioned for different droplet volumes. Hence, channel confined droplets of about 30–40 nL from the first network part were expanded to cannel confined droplets of about 500 to about 2500 nL in the second network part. Four different operation modes were realized: (a) flow rate independent droplet formation in a self-controlled way caused by the bypassed chamber design, (b) single droplet expansion mode, (c) multiple droplet expansion mode, and (d) multiple droplet coalescence mode. The last mode was used for the automated coalescence of 12 droplets of about 40 nL volume to produce a highly ordered output sequence with individual droplet volumes of about 500 nL volume. The experimental investigation confirmed a high tolerance of the developed chamber against the variation of key parameters of the dispersed-phase like salt content, pH value and fluid viscosity. The presented fluidic chamber provides a solution for the problem of bridging different droplet volumes in a fluidic network. |
format | Online Article Text |
id | pubmed-7231328 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-72313282020-05-22 Microfluidic Chamber Design for Controlled Droplet Expansion and Coalescence Kielpinski, Mark Walther, Oliver Cao, Jialan Henkel, Thomas Köhler, J. Michael Groß, G. Alexander Micromachines (Basel) Article The defined formation and expansion of droplets are essential operations for droplet-based screening assays. The volumetric expansion of droplets causes a dilution of the ingredients. Dilution is required for the generation of concentration graduation which is mandatory for many different assay protocols. Here, we describe the design of a microfluidic operation unit based on a bypassed chamber and its operation modes. The different operation modes enable the defined formation of sub-µL droplets on the one hand and the expansion of low nL to sub-µL droplets by controlled coalescence on the other. In this way the chamber acts as fluidic interface between two fluidic network parts dimensioned for different droplet volumes. Hence, channel confined droplets of about 30–40 nL from the first network part were expanded to cannel confined droplets of about 500 to about 2500 nL in the second network part. Four different operation modes were realized: (a) flow rate independent droplet formation in a self-controlled way caused by the bypassed chamber design, (b) single droplet expansion mode, (c) multiple droplet expansion mode, and (d) multiple droplet coalescence mode. The last mode was used for the automated coalescence of 12 droplets of about 40 nL volume to produce a highly ordered output sequence with individual droplet volumes of about 500 nL volume. The experimental investigation confirmed a high tolerance of the developed chamber against the variation of key parameters of the dispersed-phase like salt content, pH value and fluid viscosity. The presented fluidic chamber provides a solution for the problem of bridging different droplet volumes in a fluidic network. MDPI 2020-04-10 /pmc/articles/PMC7231328/ /pubmed/32290165 http://dx.doi.org/10.3390/mi11040394 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Kielpinski, Mark Walther, Oliver Cao, Jialan Henkel, Thomas Köhler, J. Michael Groß, G. Alexander Microfluidic Chamber Design for Controlled Droplet Expansion and Coalescence |
title | Microfluidic Chamber Design for Controlled Droplet Expansion and Coalescence |
title_full | Microfluidic Chamber Design for Controlled Droplet Expansion and Coalescence |
title_fullStr | Microfluidic Chamber Design for Controlled Droplet Expansion and Coalescence |
title_full_unstemmed | Microfluidic Chamber Design for Controlled Droplet Expansion and Coalescence |
title_short | Microfluidic Chamber Design for Controlled Droplet Expansion and Coalescence |
title_sort | microfluidic chamber design for controlled droplet expansion and coalescence |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7231328/ https://www.ncbi.nlm.nih.gov/pubmed/32290165 http://dx.doi.org/10.3390/mi11040394 |
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