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Acrylic Acid Plasma Coated 3D Scaffolds for Cartilage tissue engineering applications

The current generation of tissue engineered additive manufactured scaffolds for cartilage repair shows high potential for growing adult cartilage tissue. This study proposes two surface modification strategies based on non-thermal plasma technology for the modification of poly(ethylene oxide terepht...

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Autores principales: Cools, Pieter, Mota, Carlos, Lorenzo-Moldero, Ivan, Ghobeira, Rouba, De Geyter, Nathalie, Moroni, Lorenzo, Morent, Rino
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5832775/
https://www.ncbi.nlm.nih.gov/pubmed/29497176
http://dx.doi.org/10.1038/s41598-018-22301-0
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author Cools, Pieter
Mota, Carlos
Lorenzo-Moldero, Ivan
Ghobeira, Rouba
De Geyter, Nathalie
Moroni, Lorenzo
Morent, Rino
author_facet Cools, Pieter
Mota, Carlos
Lorenzo-Moldero, Ivan
Ghobeira, Rouba
De Geyter, Nathalie
Moroni, Lorenzo
Morent, Rino
author_sort Cools, Pieter
collection PubMed
description The current generation of tissue engineered additive manufactured scaffolds for cartilage repair shows high potential for growing adult cartilage tissue. This study proposes two surface modification strategies based on non-thermal plasma technology for the modification of poly(ethylene oxide terephthalate/poly(butylene terephthalate) additive manufactured scaffolds to enhance their cell-material interactions. The first, plasma activation in a helium discharge, introduced non-specific polar functionalities. In the second approach, a carboxylic acid plasma polymer coating, using acrylic acid as precursor, was deposited throughout the scaffolds. Both surface modifications were characterized by significant changes in wettability, linked to the incorporation of new oxygen-containing functional groups. Their capacity for chondrogenesis was studied using ATDC5 chondroblasts as a model cell-line. The results demonstrate that the carboxylic acid-rich plasma coating had a positive effect on the generation of the glucoaminoglycans (GAG) matrix and stimulated the migration of cells throughout the scaffold. He plasma activation stimulated the formation of GAGs but did not stimulate the migration of chondroblasts throughout the scaffolds. Both plasma treatments spurred chondrogenesis by favoring GAG deposition. This leads to the overall conclusion that acrylic acid based plasma coatings exhibit potential as a surface modification technique for cartilage tissue engineering applications.
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spelling pubmed-58327752018-03-05 Acrylic Acid Plasma Coated 3D Scaffolds for Cartilage tissue engineering applications Cools, Pieter Mota, Carlos Lorenzo-Moldero, Ivan Ghobeira, Rouba De Geyter, Nathalie Moroni, Lorenzo Morent, Rino Sci Rep Article The current generation of tissue engineered additive manufactured scaffolds for cartilage repair shows high potential for growing adult cartilage tissue. This study proposes two surface modification strategies based on non-thermal plasma technology for the modification of poly(ethylene oxide terephthalate/poly(butylene terephthalate) additive manufactured scaffolds to enhance their cell-material interactions. The first, plasma activation in a helium discharge, introduced non-specific polar functionalities. In the second approach, a carboxylic acid plasma polymer coating, using acrylic acid as precursor, was deposited throughout the scaffolds. Both surface modifications were characterized by significant changes in wettability, linked to the incorporation of new oxygen-containing functional groups. Their capacity for chondrogenesis was studied using ATDC5 chondroblasts as a model cell-line. The results demonstrate that the carboxylic acid-rich plasma coating had a positive effect on the generation of the glucoaminoglycans (GAG) matrix and stimulated the migration of cells throughout the scaffold. He plasma activation stimulated the formation of GAGs but did not stimulate the migration of chondroblasts throughout the scaffolds. Both plasma treatments spurred chondrogenesis by favoring GAG deposition. This leads to the overall conclusion that acrylic acid based plasma coatings exhibit potential as a surface modification technique for cartilage tissue engineering applications. Nature Publishing Group UK 2018-03-01 /pmc/articles/PMC5832775/ /pubmed/29497176 http://dx.doi.org/10.1038/s41598-018-22301-0 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
Cools, Pieter
Mota, Carlos
Lorenzo-Moldero, Ivan
Ghobeira, Rouba
De Geyter, Nathalie
Moroni, Lorenzo
Morent, Rino
Acrylic Acid Plasma Coated 3D Scaffolds for Cartilage tissue engineering applications
title Acrylic Acid Plasma Coated 3D Scaffolds for Cartilage tissue engineering applications
title_full Acrylic Acid Plasma Coated 3D Scaffolds for Cartilage tissue engineering applications
title_fullStr Acrylic Acid Plasma Coated 3D Scaffolds for Cartilage tissue engineering applications
title_full_unstemmed Acrylic Acid Plasma Coated 3D Scaffolds for Cartilage tissue engineering applications
title_short Acrylic Acid Plasma Coated 3D Scaffolds for Cartilage tissue engineering applications
title_sort acrylic acid plasma coated 3d scaffolds for cartilage tissue engineering applications
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5832775/
https://www.ncbi.nlm.nih.gov/pubmed/29497176
http://dx.doi.org/10.1038/s41598-018-22301-0
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