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Development of Porous and Flexible PTMC Membranes for In Vitro Organ Models Fabricated by Evaporation-Induced Phase Separation

Polymeric membranes are widely applied in biomedical applications, including in vitro organ models. In such models, they are mostly used as supports on which cells are cultured to create functional tissue units of the desired organ. To this end, the membrane properties, e.g., morphology and porosity...

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Autores principales: Pasman, Thijs, Baptista, Danielle, van Riet, Sander, Truckenmüller, Roman K., Hiemstra, Pieter S., Rottier, Robbert J., Stamatialis, Dimitrios, Poot, André A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7694515/
https://www.ncbi.nlm.nih.gov/pubmed/33167539
http://dx.doi.org/10.3390/membranes10110330
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author Pasman, Thijs
Baptista, Danielle
van Riet, Sander
Truckenmüller, Roman K.
Hiemstra, Pieter S.
Rottier, Robbert J.
Stamatialis, Dimitrios
Poot, André A.
author_facet Pasman, Thijs
Baptista, Danielle
van Riet, Sander
Truckenmüller, Roman K.
Hiemstra, Pieter S.
Rottier, Robbert J.
Stamatialis, Dimitrios
Poot, André A.
author_sort Pasman, Thijs
collection PubMed
description Polymeric membranes are widely applied in biomedical applications, including in vitro organ models. In such models, they are mostly used as supports on which cells are cultured to create functional tissue units of the desired organ. To this end, the membrane properties, e.g., morphology and porosity, should match the tissue properties. Organ models of dynamic (barrier) tissues, e.g., lung, require flexible, elastic and porous membranes. Thus, membranes based on poly (dimethyl siloxane) (PDMS) are often applied, which are flexible and elastic. However, PDMS has low cell adhesive properties and displays small molecule ad- and absorption. Furthermore, the introduction of porosity in these membranes requires elaborate methods. In this work, we aim to develop porous membranes for organ models based on poly(trimethylene carbonate) (PTMC): a flexible polymer with good cell adhesive properties which has been used for tissue engineering scaffolds, but not in in vitro organ models. For developing these membranes, we applied evaporation-induced phase separation (EIPS), a new method in this field based on solvent evaporation initiating phase separation, followed by membrane photo-crosslinking. We optimised various processing variables for obtaining form-stable PTMC membranes with average pore sizes between 5 to 8 µm and water permeance in the microfiltration range (17,000–41,000 L/m(2)/h/bar). Importantly, the membranes are flexible and are suitable for implementation in in vitro organ models.
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spelling pubmed-76945152020-11-28 Development of Porous and Flexible PTMC Membranes for In Vitro Organ Models Fabricated by Evaporation-Induced Phase Separation Pasman, Thijs Baptista, Danielle van Riet, Sander Truckenmüller, Roman K. Hiemstra, Pieter S. Rottier, Robbert J. Stamatialis, Dimitrios Poot, André A. Membranes (Basel) Article Polymeric membranes are widely applied in biomedical applications, including in vitro organ models. In such models, they are mostly used as supports on which cells are cultured to create functional tissue units of the desired organ. To this end, the membrane properties, e.g., morphology and porosity, should match the tissue properties. Organ models of dynamic (barrier) tissues, e.g., lung, require flexible, elastic and porous membranes. Thus, membranes based on poly (dimethyl siloxane) (PDMS) are often applied, which are flexible and elastic. However, PDMS has low cell adhesive properties and displays small molecule ad- and absorption. Furthermore, the introduction of porosity in these membranes requires elaborate methods. In this work, we aim to develop porous membranes for organ models based on poly(trimethylene carbonate) (PTMC): a flexible polymer with good cell adhesive properties which has been used for tissue engineering scaffolds, but not in in vitro organ models. For developing these membranes, we applied evaporation-induced phase separation (EIPS), a new method in this field based on solvent evaporation initiating phase separation, followed by membrane photo-crosslinking. We optimised various processing variables for obtaining form-stable PTMC membranes with average pore sizes between 5 to 8 µm and water permeance in the microfiltration range (17,000–41,000 L/m(2)/h/bar). Importantly, the membranes are flexible and are suitable for implementation in in vitro organ models. MDPI 2020-11-05 /pmc/articles/PMC7694515/ /pubmed/33167539 http://dx.doi.org/10.3390/membranes10110330 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Pasman, Thijs
Baptista, Danielle
van Riet, Sander
Truckenmüller, Roman K.
Hiemstra, Pieter S.
Rottier, Robbert J.
Stamatialis, Dimitrios
Poot, André A.
Development of Porous and Flexible PTMC Membranes for In Vitro Organ Models Fabricated by Evaporation-Induced Phase Separation
title Development of Porous and Flexible PTMC Membranes for In Vitro Organ Models Fabricated by Evaporation-Induced Phase Separation
title_full Development of Porous and Flexible PTMC Membranes for In Vitro Organ Models Fabricated by Evaporation-Induced Phase Separation
title_fullStr Development of Porous and Flexible PTMC Membranes for In Vitro Organ Models Fabricated by Evaporation-Induced Phase Separation
title_full_unstemmed Development of Porous and Flexible PTMC Membranes for In Vitro Organ Models Fabricated by Evaporation-Induced Phase Separation
title_short Development of Porous and Flexible PTMC Membranes for In Vitro Organ Models Fabricated by Evaporation-Induced Phase Separation
title_sort development of porous and flexible ptmc membranes for in vitro organ models fabricated by evaporation-induced phase separation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7694515/
https://www.ncbi.nlm.nih.gov/pubmed/33167539
http://dx.doi.org/10.3390/membranes10110330
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