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Upscaling of pneumatic membrane valves for the integration of 3D cell cultures on chip

Microfluidic large-scale integration (mLSI) technology enables the automation of two-dimensional (2D) cell culture processes in a highly parallel manner. Despite the wide range of biological applications of mLSI chips, manufacturing limitations of the central functional element, the pneumatic membra...

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Autores principales: Compera, Nina, Atwell, Scott, Wirth, Johannes, Wolfrum, Bernhard, Meier, Matthias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8314520/
https://www.ncbi.nlm.nih.gov/pubmed/34143169
http://dx.doi.org/10.1039/d1lc00194a
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author Compera, Nina
Atwell, Scott
Wirth, Johannes
Wolfrum, Bernhard
Meier, Matthias
author_facet Compera, Nina
Atwell, Scott
Wirth, Johannes
Wolfrum, Bernhard
Meier, Matthias
author_sort Compera, Nina
collection PubMed
description Microfluidic large-scale integration (mLSI) technology enables the automation of two-dimensional (2D) cell culture processes in a highly parallel manner. Despite the wide range of biological applications of mLSI chips, manufacturing limitations of the central functional element, the pneumatic membrane valve (PMV), make the technology inaccessible for integrating tissue cultures and organoids with dimensions larger than tens of microns. In this study, we developed microtechnology processes to upscale PMVs for mLSI chips by combining 3D printing and soft lithography. Therefore, we developed a robust soft lithography protocol for the production of polydimethylsiloxane chips with PMVs from 3D-printed acrylate and wax molds. While scaled-up PMVs manufactured from acrylate-printed molds exhibited channel profiles with staircases, owing to the inherent 3D stereolithography printing process, PMVs manufactured from reflowed wax molds exhibited a semi-half-rounded channel profile. PMVs with different channel profiles showed closing pressures between 130 and 22.5 kPa, respectively. We demonstrated the functionality of the scaled-up PMVs by forming and maintaining 3D cell cultures from mouse fibroblasts (NIH3T3), human induced pluripotent stem cells (hiPSCs), and human adipose-derived adult stem cells (hASCs), with a narrow size distribution between 124 and 136 μm. Further, parallel and serial design of PMVs on an mLSI chip is used to first form and culture 3D cell cultures before fusing them within a defined flow process. Unit cell designs with upscaled PMVs enabled parallel formation, culturing, trapping, retrieval, and fusion of 3D cell cultures. Thus, the presented additive manufacturing strategy for mLSI chips will foster new developments for highly parallel 3D cell culture screening applications.
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spelling pubmed-83145202021-08-03 Upscaling of pneumatic membrane valves for the integration of 3D cell cultures on chip Compera, Nina Atwell, Scott Wirth, Johannes Wolfrum, Bernhard Meier, Matthias Lab Chip Chemistry Microfluidic large-scale integration (mLSI) technology enables the automation of two-dimensional (2D) cell culture processes in a highly parallel manner. Despite the wide range of biological applications of mLSI chips, manufacturing limitations of the central functional element, the pneumatic membrane valve (PMV), make the technology inaccessible for integrating tissue cultures and organoids with dimensions larger than tens of microns. In this study, we developed microtechnology processes to upscale PMVs for mLSI chips by combining 3D printing and soft lithography. Therefore, we developed a robust soft lithography protocol for the production of polydimethylsiloxane chips with PMVs from 3D-printed acrylate and wax molds. While scaled-up PMVs manufactured from acrylate-printed molds exhibited channel profiles with staircases, owing to the inherent 3D stereolithography printing process, PMVs manufactured from reflowed wax molds exhibited a semi-half-rounded channel profile. PMVs with different channel profiles showed closing pressures between 130 and 22.5 kPa, respectively. We demonstrated the functionality of the scaled-up PMVs by forming and maintaining 3D cell cultures from mouse fibroblasts (NIH3T3), human induced pluripotent stem cells (hiPSCs), and human adipose-derived adult stem cells (hASCs), with a narrow size distribution between 124 and 136 μm. Further, parallel and serial design of PMVs on an mLSI chip is used to first form and culture 3D cell cultures before fusing them within a defined flow process. Unit cell designs with upscaled PMVs enabled parallel formation, culturing, trapping, retrieval, and fusion of 3D cell cultures. Thus, the presented additive manufacturing strategy for mLSI chips will foster new developments for highly parallel 3D cell culture screening applications. The Royal Society of Chemistry 2021-06-18 /pmc/articles/PMC8314520/ /pubmed/34143169 http://dx.doi.org/10.1039/d1lc00194a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Compera, Nina
Atwell, Scott
Wirth, Johannes
Wolfrum, Bernhard
Meier, Matthias
Upscaling of pneumatic membrane valves for the integration of 3D cell cultures on chip
title Upscaling of pneumatic membrane valves for the integration of 3D cell cultures on chip
title_full Upscaling of pneumatic membrane valves for the integration of 3D cell cultures on chip
title_fullStr Upscaling of pneumatic membrane valves for the integration of 3D cell cultures on chip
title_full_unstemmed Upscaling of pneumatic membrane valves for the integration of 3D cell cultures on chip
title_short Upscaling of pneumatic membrane valves for the integration of 3D cell cultures on chip
title_sort upscaling of pneumatic membrane valves for the integration of 3d cell cultures on chip
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8314520/
https://www.ncbi.nlm.nih.gov/pubmed/34143169
http://dx.doi.org/10.1039/d1lc00194a
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