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Hydrogel-based microfluidic device with multiplexed 3D in vitro cell culture

Microfluidic devices that combine an extracellular matrix environment, cells, and physiologically relevant perfusion, are advantageous as cell culture platforms. We developed a hydrogel-based, microfluidic cell culture platform by loading polyethylene glycol (PEG) hydrogel-encapsulated U87 glioblast...

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Autores principales: Clancy, Allison, Chen, Dayi, Bruns, Joseph, Nadella, Jahnavi, Stealey, Samuel, Zhang, Yanjia, Timperman, Aaron, Zustiak, Silviya P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9588086/
https://www.ncbi.nlm.nih.gov/pubmed/36273031
http://dx.doi.org/10.1038/s41598-022-22439-y
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author Clancy, Allison
Chen, Dayi
Bruns, Joseph
Nadella, Jahnavi
Stealey, Samuel
Zhang, Yanjia
Timperman, Aaron
Zustiak, Silviya P.
author_facet Clancy, Allison
Chen, Dayi
Bruns, Joseph
Nadella, Jahnavi
Stealey, Samuel
Zhang, Yanjia
Timperman, Aaron
Zustiak, Silviya P.
author_sort Clancy, Allison
collection PubMed
description Microfluidic devices that combine an extracellular matrix environment, cells, and physiologically relevant perfusion, are advantageous as cell culture platforms. We developed a hydrogel-based, microfluidic cell culture platform by loading polyethylene glycol (PEG) hydrogel-encapsulated U87 glioblastoma cells into membrane-capped wells in polydimethyl siloxane (PDMS). The multilayer microfluidic cell culture system combines previously reported design features in a configuration that loads and biomimetically perfuses a 2D array of cell culture chambers. One dimension of the array is fed by a microfluidic concentration gradient generator (MCGG) while the orthogonal dimension provides loading channels that fill rows of cell culture chambers in a separate layer. In contrast to typical tree-like MCGG mixers, a fractional serial dilution of 1, ½, ¼, and 0 of the initial solute concentration is achieved by tailoring the input microchannel widths. Hydrogels are efficiently and reproducibly loaded in all wells and cells are evenly distributed throughout the hydrogel, maintaining > 90% viability for up to 4 days. In a drug screening assay, diffusion of temozolomide and carmustine to hydrogel-encapsulated U87 cells from the perfusion solution is measured, and dose–response curves are generated, demonstrating utility as an in vitro mimic of the glioblastoma microenvironment.
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spelling pubmed-95880862022-10-24 Hydrogel-based microfluidic device with multiplexed 3D in vitro cell culture Clancy, Allison Chen, Dayi Bruns, Joseph Nadella, Jahnavi Stealey, Samuel Zhang, Yanjia Timperman, Aaron Zustiak, Silviya P. Sci Rep Article Microfluidic devices that combine an extracellular matrix environment, cells, and physiologically relevant perfusion, are advantageous as cell culture platforms. We developed a hydrogel-based, microfluidic cell culture platform by loading polyethylene glycol (PEG) hydrogel-encapsulated U87 glioblastoma cells into membrane-capped wells in polydimethyl siloxane (PDMS). The multilayer microfluidic cell culture system combines previously reported design features in a configuration that loads and biomimetically perfuses a 2D array of cell culture chambers. One dimension of the array is fed by a microfluidic concentration gradient generator (MCGG) while the orthogonal dimension provides loading channels that fill rows of cell culture chambers in a separate layer. In contrast to typical tree-like MCGG mixers, a fractional serial dilution of 1, ½, ¼, and 0 of the initial solute concentration is achieved by tailoring the input microchannel widths. Hydrogels are efficiently and reproducibly loaded in all wells and cells are evenly distributed throughout the hydrogel, maintaining > 90% viability for up to 4 days. In a drug screening assay, diffusion of temozolomide and carmustine to hydrogel-encapsulated U87 cells from the perfusion solution is measured, and dose–response curves are generated, demonstrating utility as an in vitro mimic of the glioblastoma microenvironment. Nature Publishing Group UK 2022-10-22 /pmc/articles/PMC9588086/ /pubmed/36273031 http://dx.doi.org/10.1038/s41598-022-22439-y Text en © The Author(s) 2022 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Clancy, Allison
Chen, Dayi
Bruns, Joseph
Nadella, Jahnavi
Stealey, Samuel
Zhang, Yanjia
Timperman, Aaron
Zustiak, Silviya P.
Hydrogel-based microfluidic device with multiplexed 3D in vitro cell culture
title Hydrogel-based microfluidic device with multiplexed 3D in vitro cell culture
title_full Hydrogel-based microfluidic device with multiplexed 3D in vitro cell culture
title_fullStr Hydrogel-based microfluidic device with multiplexed 3D in vitro cell culture
title_full_unstemmed Hydrogel-based microfluidic device with multiplexed 3D in vitro cell culture
title_short Hydrogel-based microfluidic device with multiplexed 3D in vitro cell culture
title_sort hydrogel-based microfluidic device with multiplexed 3d in vitro cell culture
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9588086/
https://www.ncbi.nlm.nih.gov/pubmed/36273031
http://dx.doi.org/10.1038/s41598-022-22439-y
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