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3D‐Printed Soft Lithography for Complex Compartmentalized Microfluidic Neural Devices
Compartmentalized microfluidic platforms are an invaluable tool in neuroscience research. However, harnessing the full potential of this technology remains hindered by the lack of a simple fabrication approach for the creation of intricate device architectures with high‐aspect ratio features. Here,...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7435242/ https://www.ncbi.nlm.nih.gov/pubmed/32832365 http://dx.doi.org/10.1002/advs.202001150 |
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author | Kajtez, Janko Buchmann, Sebastian Vasudevan, Shashank Birtele, Marcella Rocchetti, Stefano Pless, Christian Jonathan Heiskanen, Arto Barker, Roger A. Martínez‐Serrano, Alberto Parmar, Malin Lind, Johan Ulrik Emnéus, Jenny |
author_facet | Kajtez, Janko Buchmann, Sebastian Vasudevan, Shashank Birtele, Marcella Rocchetti, Stefano Pless, Christian Jonathan Heiskanen, Arto Barker, Roger A. Martínez‐Serrano, Alberto Parmar, Malin Lind, Johan Ulrik Emnéus, Jenny |
author_sort | Kajtez, Janko |
collection | PubMed |
description | Compartmentalized microfluidic platforms are an invaluable tool in neuroscience research. However, harnessing the full potential of this technology remains hindered by the lack of a simple fabrication approach for the creation of intricate device architectures with high‐aspect ratio features. Here, a hybrid additive manufacturing approach is presented for the fabrication of open‐well compartmentalized neural devices that provides larger freedom of device design, removes the need for manual postprocessing, and allows an increase in the biocompatibility of the system. Suitability of the method for multimaterial integration allows to tailor the device architecture for the long‐term maintenance of healthy human stem‐cell derived neurons and astrocytes, spanning at least 40 days. Leveraging fast‐prototyping capabilities at both micro and macroscale, a proof‐of‐principle human in vitro model of the nigrostriatal pathway is created. By presenting a route for novel materials and unique architectures in microfluidic systems, the method provides new possibilities in biological research beyond neuroscience applications. |
format | Online Article Text |
id | pubmed-7435242 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-74352422020-08-20 3D‐Printed Soft Lithography for Complex Compartmentalized Microfluidic Neural Devices Kajtez, Janko Buchmann, Sebastian Vasudevan, Shashank Birtele, Marcella Rocchetti, Stefano Pless, Christian Jonathan Heiskanen, Arto Barker, Roger A. Martínez‐Serrano, Alberto Parmar, Malin Lind, Johan Ulrik Emnéus, Jenny Adv Sci (Weinh) Full Papers Compartmentalized microfluidic platforms are an invaluable tool in neuroscience research. However, harnessing the full potential of this technology remains hindered by the lack of a simple fabrication approach for the creation of intricate device architectures with high‐aspect ratio features. Here, a hybrid additive manufacturing approach is presented for the fabrication of open‐well compartmentalized neural devices that provides larger freedom of device design, removes the need for manual postprocessing, and allows an increase in the biocompatibility of the system. Suitability of the method for multimaterial integration allows to tailor the device architecture for the long‐term maintenance of healthy human stem‐cell derived neurons and astrocytes, spanning at least 40 days. Leveraging fast‐prototyping capabilities at both micro and macroscale, a proof‐of‐principle human in vitro model of the nigrostriatal pathway is created. By presenting a route for novel materials and unique architectures in microfluidic systems, the method provides new possibilities in biological research beyond neuroscience applications. John Wiley and Sons Inc. 2020-06-15 /pmc/articles/PMC7435242/ /pubmed/32832365 http://dx.doi.org/10.1002/advs.202001150 Text en © 2020 The Authors. Published by WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Full Papers Kajtez, Janko Buchmann, Sebastian Vasudevan, Shashank Birtele, Marcella Rocchetti, Stefano Pless, Christian Jonathan Heiskanen, Arto Barker, Roger A. Martínez‐Serrano, Alberto Parmar, Malin Lind, Johan Ulrik Emnéus, Jenny 3D‐Printed Soft Lithography for Complex Compartmentalized Microfluidic Neural Devices |
title | 3D‐Printed Soft Lithography for Complex Compartmentalized Microfluidic Neural Devices |
title_full | 3D‐Printed Soft Lithography for Complex Compartmentalized Microfluidic Neural Devices |
title_fullStr | 3D‐Printed Soft Lithography for Complex Compartmentalized Microfluidic Neural Devices |
title_full_unstemmed | 3D‐Printed Soft Lithography for Complex Compartmentalized Microfluidic Neural Devices |
title_short | 3D‐Printed Soft Lithography for Complex Compartmentalized Microfluidic Neural Devices |
title_sort | 3d‐printed soft lithography for complex compartmentalized microfluidic neural devices |
topic | Full Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7435242/ https://www.ncbi.nlm.nih.gov/pubmed/32832365 http://dx.doi.org/10.1002/advs.202001150 |
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