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A Fast Alternative to Soft Lithography for the Fabrication of Organ‐on‐a‐Chip Elastomeric‐Based Devices and Microactuators
Organ‐on‐a‐chip technology promises to revolutionize how pre‐clinical human trials are conducted. Engineering an in vitro environment that mimics the functionality and architecture of human physiology is essential toward building better platforms for drug development and personalized medicine. Howev...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8061392/ https://www.ncbi.nlm.nih.gov/pubmed/33898174 http://dx.doi.org/10.1002/advs.202003273 |
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author | Ferreira, Daniel A. Rothbauer, Mario Conde, João P. Ertl, Peter Oliveira, Carla Granja, Pedro L. |
author_facet | Ferreira, Daniel A. Rothbauer, Mario Conde, João P. Ertl, Peter Oliveira, Carla Granja, Pedro L. |
author_sort | Ferreira, Daniel A. |
collection | PubMed |
description | Organ‐on‐a‐chip technology promises to revolutionize how pre‐clinical human trials are conducted. Engineering an in vitro environment that mimics the functionality and architecture of human physiology is essential toward building better platforms for drug development and personalized medicine. However, the complex nature of these devices requires specialized, time consuming, and expensive fabrication methodologies. Alternatives that reduce design‐to‐prototype time are needed, in order to fulfill the potential of these devices. Here, a streamlined approach is proposed for the fabrication of organ‐on‐a‐chip devices with incorporated microactuators, by using an adaptation of xurography. This method can generate multilayered, membrane‐integrated biochips in a matter of hours, using low‐cost benchtop equipment. These devices are capable of withstanding considerable pressure without delamination. Furthermore, this method is suitable for the integration of flexible membranes, required for organ‐on‐a‐chip applications, such as mechanical actuation or the establishment of biological barrier function. The devices are compatible with cell culture applications and present no cytotoxic effects or observable alterations on cellular homeostasis. This fabrication method can rapidly generate organ‐on‐a‐chip prototypes for a fraction of cost and time, in comparison to conventional soft lithography, constituting an interesting alternative to the current fabrication methods. |
format | Online Article Text |
id | pubmed-8061392 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-80613922021-04-23 A Fast Alternative to Soft Lithography for the Fabrication of Organ‐on‐a‐Chip Elastomeric‐Based Devices and Microactuators Ferreira, Daniel A. Rothbauer, Mario Conde, João P. Ertl, Peter Oliveira, Carla Granja, Pedro L. Adv Sci (Weinh) Full Papers Organ‐on‐a‐chip technology promises to revolutionize how pre‐clinical human trials are conducted. Engineering an in vitro environment that mimics the functionality and architecture of human physiology is essential toward building better platforms for drug development and personalized medicine. However, the complex nature of these devices requires specialized, time consuming, and expensive fabrication methodologies. Alternatives that reduce design‐to‐prototype time are needed, in order to fulfill the potential of these devices. Here, a streamlined approach is proposed for the fabrication of organ‐on‐a‐chip devices with incorporated microactuators, by using an adaptation of xurography. This method can generate multilayered, membrane‐integrated biochips in a matter of hours, using low‐cost benchtop equipment. These devices are capable of withstanding considerable pressure without delamination. Furthermore, this method is suitable for the integration of flexible membranes, required for organ‐on‐a‐chip applications, such as mechanical actuation or the establishment of biological barrier function. The devices are compatible with cell culture applications and present no cytotoxic effects or observable alterations on cellular homeostasis. This fabrication method can rapidly generate organ‐on‐a‐chip prototypes for a fraction of cost and time, in comparison to conventional soft lithography, constituting an interesting alternative to the current fabrication methods. John Wiley and Sons Inc. 2021-02-08 /pmc/articles/PMC8061392/ /pubmed/33898174 http://dx.doi.org/10.1002/advs.202003273 Text en © 2021 The Authors. Advanced Science published by Wiley‐VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://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 Ferreira, Daniel A. Rothbauer, Mario Conde, João P. Ertl, Peter Oliveira, Carla Granja, Pedro L. A Fast Alternative to Soft Lithography for the Fabrication of Organ‐on‐a‐Chip Elastomeric‐Based Devices and Microactuators |
title | A Fast Alternative to Soft Lithography for the Fabrication of Organ‐on‐a‐Chip Elastomeric‐Based Devices and Microactuators |
title_full | A Fast Alternative to Soft Lithography for the Fabrication of Organ‐on‐a‐Chip Elastomeric‐Based Devices and Microactuators |
title_fullStr | A Fast Alternative to Soft Lithography for the Fabrication of Organ‐on‐a‐Chip Elastomeric‐Based Devices and Microactuators |
title_full_unstemmed | A Fast Alternative to Soft Lithography for the Fabrication of Organ‐on‐a‐Chip Elastomeric‐Based Devices and Microactuators |
title_short | A Fast Alternative to Soft Lithography for the Fabrication of Organ‐on‐a‐Chip Elastomeric‐Based Devices and Microactuators |
title_sort | fast alternative to soft lithography for the fabrication of organ‐on‐a‐chip elastomeric‐based devices and microactuators |
topic | Full Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8061392/ https://www.ncbi.nlm.nih.gov/pubmed/33898174 http://dx.doi.org/10.1002/advs.202003273 |
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