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Silicon-Based 3D Microfluidics for Parallelization of Droplet Generation
Both the diversity and complexity of microfluidic systems have experienced a tremendous progress over the last decades, enabled by new materials, novel device concepts and innovative fabrication routes. In particular the subfield of high-throughput screening, used for biochemical, genetic and pharma...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10386391/ https://www.ncbi.nlm.nih.gov/pubmed/37512600 http://dx.doi.org/10.3390/mi14071289 |
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author | Monserrat Lopez, Diego Rottmann, Philipp Fussenegger, Martin Lörtscher, Emanuel |
author_facet | Monserrat Lopez, Diego Rottmann, Philipp Fussenegger, Martin Lörtscher, Emanuel |
author_sort | Monserrat Lopez, Diego |
collection | PubMed |
description | Both the diversity and complexity of microfluidic systems have experienced a tremendous progress over the last decades, enabled by new materials, novel device concepts and innovative fabrication routes. In particular the subfield of high-throughput screening, used for biochemical, genetic and pharmacological samples, has extensively emerged from developments in droplet microfluidics. More recently, new 3D device architectures enabled either by stacking layers of PDMS or by direct 3D-printing have gained enormous attention for applications in chemical synthesis or biomedical assays. While the first microfluidic devices were based on silicon and glass structures, those materials have not yet been significantly expanded towards 3D despite their high chemical compatibility, mechanical strength or mass-production potential. In our work, we present a generic fabrication route based on the implementation of vertical vias and a redistribution layer to create glass–silicon–glass 3D microfluidic structures. It is used to build different droplet-generating devices with several flow-focusing junctions in parallel, all fed from a single source. We study the effect of having several of these junctions in parallel by varying the flow conditions of both the continuous and the dispersed phases. We demonstrate that the generic concept enables an upscaling in the production rate by increasing the number of droplet generators per device without sacrificing the monodispersity of the droplets. |
format | Online Article Text |
id | pubmed-10386391 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-103863912023-07-30 Silicon-Based 3D Microfluidics for Parallelization of Droplet Generation Monserrat Lopez, Diego Rottmann, Philipp Fussenegger, Martin Lörtscher, Emanuel Micromachines (Basel) Article Both the diversity and complexity of microfluidic systems have experienced a tremendous progress over the last decades, enabled by new materials, novel device concepts and innovative fabrication routes. In particular the subfield of high-throughput screening, used for biochemical, genetic and pharmacological samples, has extensively emerged from developments in droplet microfluidics. More recently, new 3D device architectures enabled either by stacking layers of PDMS or by direct 3D-printing have gained enormous attention for applications in chemical synthesis or biomedical assays. While the first microfluidic devices were based on silicon and glass structures, those materials have not yet been significantly expanded towards 3D despite their high chemical compatibility, mechanical strength or mass-production potential. In our work, we present a generic fabrication route based on the implementation of vertical vias and a redistribution layer to create glass–silicon–glass 3D microfluidic structures. It is used to build different droplet-generating devices with several flow-focusing junctions in parallel, all fed from a single source. We study the effect of having several of these junctions in parallel by varying the flow conditions of both the continuous and the dispersed phases. We demonstrate that the generic concept enables an upscaling in the production rate by increasing the number of droplet generators per device without sacrificing the monodispersity of the droplets. MDPI 2023-06-23 /pmc/articles/PMC10386391/ /pubmed/37512600 http://dx.doi.org/10.3390/mi14071289 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Monserrat Lopez, Diego Rottmann, Philipp Fussenegger, Martin Lörtscher, Emanuel Silicon-Based 3D Microfluidics for Parallelization of Droplet Generation |
title | Silicon-Based 3D Microfluidics for Parallelization of Droplet Generation |
title_full | Silicon-Based 3D Microfluidics for Parallelization of Droplet Generation |
title_fullStr | Silicon-Based 3D Microfluidics for Parallelization of Droplet Generation |
title_full_unstemmed | Silicon-Based 3D Microfluidics for Parallelization of Droplet Generation |
title_short | Silicon-Based 3D Microfluidics for Parallelization of Droplet Generation |
title_sort | silicon-based 3d microfluidics for parallelization of droplet generation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10386391/ https://www.ncbi.nlm.nih.gov/pubmed/37512600 http://dx.doi.org/10.3390/mi14071289 |
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