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Modular operation of microfluidic chips for highly parallelized cell culture and liquid dosing via a fluidic circuit board
Microfluidic systems enable automated and highly parallelized cell culture with low volumes and defined liquid dosing. To achieve this, systems typically integrate all functions into a single, monolithic device as a “one size fits all” solution. However, this approach limits the end users’ (re)desig...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8433198/ https://www.ncbi.nlm.nih.gov/pubmed/34567716 http://dx.doi.org/10.1038/s41378-020-00216-z |
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author | Vollertsen, A. R. de Boer, D. Dekker, S. Wesselink, B. A. M. Haverkate, R. Rho, H. S. Boom, R. J. Skolimowski, M. Blom, M. Passier, R. van den Berg, A. van der Meer, A. D. Odijk, M. |
author_facet | Vollertsen, A. R. de Boer, D. Dekker, S. Wesselink, B. A. M. Haverkate, R. Rho, H. S. Boom, R. J. Skolimowski, M. Blom, M. Passier, R. van den Berg, A. van der Meer, A. D. Odijk, M. |
author_sort | Vollertsen, A. R. |
collection | PubMed |
description | Microfluidic systems enable automated and highly parallelized cell culture with low volumes and defined liquid dosing. To achieve this, systems typically integrate all functions into a single, monolithic device as a “one size fits all” solution. However, this approach limits the end users’ (re)design flexibility and complicates the addition of new functions to the system. To address this challenge, we propose and demonstrate a modular and standardized plug-and-play fluidic circuit board (FCB) for operating microfluidic building blocks (MFBBs), whereby both the FCB and the MFBBs contain integrated valves. A single FCB can parallelize up to three MFBBs of the same design or operate MFBBs with entirely different architectures. The operation of the MFBBs through the FCB is fully automated and does not incur the cost of an extra external footprint. We use this modular platform to control three microfluidic large-scale integration (mLSI) MFBBs, each of which features 64 microchambers suitable for cell culturing with high spatiotemporal control. We show as a proof of principle that we can culture human umbilical vein endothelial cells (HUVECs) for multiple days in the chambers of this MFBB. Moreover, we also use the same FCB to control an MFBB for liquid dosing with a high dynamic range. Our results demonstrate that MFBBs with different designs can be controlled and combined on a single FCB. Our novel modular approach to operating an automated microfluidic system for parallelized cell culture will enable greater experimental flexibility and facilitate the cooperation of different chips from different labs. |
format | Online Article Text |
id | pubmed-8433198 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-84331982021-09-24 Modular operation of microfluidic chips for highly parallelized cell culture and liquid dosing via a fluidic circuit board Vollertsen, A. R. de Boer, D. Dekker, S. Wesselink, B. A. M. Haverkate, R. Rho, H. S. Boom, R. J. Skolimowski, M. Blom, M. Passier, R. van den Berg, A. van der Meer, A. D. Odijk, M. Microsyst Nanoeng Article Microfluidic systems enable automated and highly parallelized cell culture with low volumes and defined liquid dosing. To achieve this, systems typically integrate all functions into a single, monolithic device as a “one size fits all” solution. However, this approach limits the end users’ (re)design flexibility and complicates the addition of new functions to the system. To address this challenge, we propose and demonstrate a modular and standardized plug-and-play fluidic circuit board (FCB) for operating microfluidic building blocks (MFBBs), whereby both the FCB and the MFBBs contain integrated valves. A single FCB can parallelize up to three MFBBs of the same design or operate MFBBs with entirely different architectures. The operation of the MFBBs through the FCB is fully automated and does not incur the cost of an extra external footprint. We use this modular platform to control three microfluidic large-scale integration (mLSI) MFBBs, each of which features 64 microchambers suitable for cell culturing with high spatiotemporal control. We show as a proof of principle that we can culture human umbilical vein endothelial cells (HUVECs) for multiple days in the chambers of this MFBB. Moreover, we also use the same FCB to control an MFBB for liquid dosing with a high dynamic range. Our results demonstrate that MFBBs with different designs can be controlled and combined on a single FCB. Our novel modular approach to operating an automated microfluidic system for parallelized cell culture will enable greater experimental flexibility and facilitate the cooperation of different chips from different labs. Nature Publishing Group UK 2020-11-30 /pmc/articles/PMC8433198/ /pubmed/34567716 http://dx.doi.org/10.1038/s41378-020-00216-z Text en © The Author(s) 2020 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Vollertsen, A. R. de Boer, D. Dekker, S. Wesselink, B. A. M. Haverkate, R. Rho, H. S. Boom, R. J. Skolimowski, M. Blom, M. Passier, R. van den Berg, A. van der Meer, A. D. Odijk, M. Modular operation of microfluidic chips for highly parallelized cell culture and liquid dosing via a fluidic circuit board |
title | Modular operation of microfluidic chips for highly parallelized cell culture and liquid dosing via a fluidic circuit board |
title_full | Modular operation of microfluidic chips for highly parallelized cell culture and liquid dosing via a fluidic circuit board |
title_fullStr | Modular operation of microfluidic chips for highly parallelized cell culture and liquid dosing via a fluidic circuit board |
title_full_unstemmed | Modular operation of microfluidic chips for highly parallelized cell culture and liquid dosing via a fluidic circuit board |
title_short | Modular operation of microfluidic chips for highly parallelized cell culture and liquid dosing via a fluidic circuit board |
title_sort | modular operation of microfluidic chips for highly parallelized cell culture and liquid dosing via a fluidic circuit board |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8433198/ https://www.ncbi.nlm.nih.gov/pubmed/34567716 http://dx.doi.org/10.1038/s41378-020-00216-z |
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