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Microfabricated tuneable and transferable porous PDMS membranes for Organs-on-Chips
We present a novel and highly reproducible process to fabricate transferable porous PDMS membranes for PDMS-based Organs-on-Chips (OOCs) using microelectromechanical systems (MEMS) fabrication technologies. Porous PDMS membranes with pore sizes down to 2.0 μm in diameter and a wide porosity range (2...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6131253/ https://www.ncbi.nlm.nih.gov/pubmed/30202042 http://dx.doi.org/10.1038/s41598-018-31912-6 |
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author | Quirós-Solano, W. F. Gaio, N. Stassen, O. M. J. A. Arik, Y. B. Silvestri, C. Van Engeland, N. C. A. Van der Meer, A. Passier, R. Sahlgren, C. M. Bouten, C. V. C. van den Berg, A. Dekker, R. Sarro, P. M. |
author_facet | Quirós-Solano, W. F. Gaio, N. Stassen, O. M. J. A. Arik, Y. B. Silvestri, C. Van Engeland, N. C. A. Van der Meer, A. Passier, R. Sahlgren, C. M. Bouten, C. V. C. van den Berg, A. Dekker, R. Sarro, P. M. |
author_sort | Quirós-Solano, W. F. |
collection | PubMed |
description | We present a novel and highly reproducible process to fabricate transferable porous PDMS membranes for PDMS-based Organs-on-Chips (OOCs) using microelectromechanical systems (MEMS) fabrication technologies. Porous PDMS membranes with pore sizes down to 2.0 μm in diameter and a wide porosity range (2–65%) can be fabricated. To overcome issues normally faced when using replica moulding and extend the applicability to most OOCs and improve their scalability and reproducibility, the process includes a sacrificial layer to easily transfer the membranes from a silicon carrier to any PDMS-based OOC. The highly reliable fabrication and transfer method does not need of manual handling to define the pore features (size, distribution), allowing very thin (<10 μm) functional membranes to be transferred at chip level with a high success rate (85%). The viability of cell culturing on the porous membranes was assessed by culturing two different cell types on transferred membranes in two different OOCs. Human umbilical endothelial cells (HUVEC) and MDA-MB-231 (MDA) cells were successfully cultured confirming the viability of cell culturing and the biocompatibility of the membranes. The results demonstrate the potential of controlling the porous membrane features to study cell mechanisms such as transmigrations, monolayer formation, and barrier function. The high control over the membrane characteristics might consequently allow to intentionally trigger or prevent certain cellular responses or mechanisms when studying human physiology and pathology using OOCs. |
format | Online Article Text |
id | pubmed-6131253 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-61312532018-09-13 Microfabricated tuneable and transferable porous PDMS membranes for Organs-on-Chips Quirós-Solano, W. F. Gaio, N. Stassen, O. M. J. A. Arik, Y. B. Silvestri, C. Van Engeland, N. C. A. Van der Meer, A. Passier, R. Sahlgren, C. M. Bouten, C. V. C. van den Berg, A. Dekker, R. Sarro, P. M. Sci Rep Article We present a novel and highly reproducible process to fabricate transferable porous PDMS membranes for PDMS-based Organs-on-Chips (OOCs) using microelectromechanical systems (MEMS) fabrication technologies. Porous PDMS membranes with pore sizes down to 2.0 μm in diameter and a wide porosity range (2–65%) can be fabricated. To overcome issues normally faced when using replica moulding and extend the applicability to most OOCs and improve their scalability and reproducibility, the process includes a sacrificial layer to easily transfer the membranes from a silicon carrier to any PDMS-based OOC. The highly reliable fabrication and transfer method does not need of manual handling to define the pore features (size, distribution), allowing very thin (<10 μm) functional membranes to be transferred at chip level with a high success rate (85%). The viability of cell culturing on the porous membranes was assessed by culturing two different cell types on transferred membranes in two different OOCs. Human umbilical endothelial cells (HUVEC) and MDA-MB-231 (MDA) cells were successfully cultured confirming the viability of cell culturing and the biocompatibility of the membranes. The results demonstrate the potential of controlling the porous membrane features to study cell mechanisms such as transmigrations, monolayer formation, and barrier function. The high control over the membrane characteristics might consequently allow to intentionally trigger or prevent certain cellular responses or mechanisms when studying human physiology and pathology using OOCs. Nature Publishing Group UK 2018-09-10 /pmc/articles/PMC6131253/ /pubmed/30202042 http://dx.doi.org/10.1038/s41598-018-31912-6 Text en © The Author(s) 2018 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/. |
spellingShingle | Article Quirós-Solano, W. F. Gaio, N. Stassen, O. M. J. A. Arik, Y. B. Silvestri, C. Van Engeland, N. C. A. Van der Meer, A. Passier, R. Sahlgren, C. M. Bouten, C. V. C. van den Berg, A. Dekker, R. Sarro, P. M. Microfabricated tuneable and transferable porous PDMS membranes for Organs-on-Chips |
title | Microfabricated tuneable and transferable porous PDMS membranes for Organs-on-Chips |
title_full | Microfabricated tuneable and transferable porous PDMS membranes for Organs-on-Chips |
title_fullStr | Microfabricated tuneable and transferable porous PDMS membranes for Organs-on-Chips |
title_full_unstemmed | Microfabricated tuneable and transferable porous PDMS membranes for Organs-on-Chips |
title_short | Microfabricated tuneable and transferable porous PDMS membranes for Organs-on-Chips |
title_sort | microfabricated tuneable and transferable porous pdms membranes for organs-on-chips |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6131253/ https://www.ncbi.nlm.nih.gov/pubmed/30202042 http://dx.doi.org/10.1038/s41598-018-31912-6 |
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