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A Preliminary Evaluation of the Pro-Chondrogenic Potential of 3D-Bioprinted Poly(ester Urea) Scaffolds
Degeneration of articular cartilage (AC) is a common healthcare issue that can result in significantly impaired function and mobility for affected patients. The avascular nature of the tissue strongly burdens its regenerative capacity contributing to the development of more serious conditions such a...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7408263/ https://www.ncbi.nlm.nih.gov/pubmed/32630145 http://dx.doi.org/10.3390/polym12071478 |
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author | Moxon, Samuel R. Ferreira, Miguel J.S. dos Santos, Patricia Popa, Bogdan Gloria, Antonio Katsarava, Ramaz Tugushi, David Serra, Armenio C. Hooper, Nigel M. Kimber, Susan J. Fonseca, Ana C. Domingos, Marco A. N. |
author_facet | Moxon, Samuel R. Ferreira, Miguel J.S. dos Santos, Patricia Popa, Bogdan Gloria, Antonio Katsarava, Ramaz Tugushi, David Serra, Armenio C. Hooper, Nigel M. Kimber, Susan J. Fonseca, Ana C. Domingos, Marco A. N. |
author_sort | Moxon, Samuel R. |
collection | PubMed |
description | Degeneration of articular cartilage (AC) is a common healthcare issue that can result in significantly impaired function and mobility for affected patients. The avascular nature of the tissue strongly burdens its regenerative capacity contributing to the development of more serious conditions such as osteoarthritis. Recent advances in bioprinting have prompted the development of alternative tissue engineering therapies for the generation of AC. Particular interest has been dedicated to scaffold-based strategies where 3D substrates are used to guide cellular function and tissue ingrowth. Despite its extensive use in bioprinting, the application of polycaprolactone (PCL) in AC is, however, restricted by properties that inhibit pro-chondrogenic cell phenotypes. This study proposes the use of a new bioprintable poly(ester urea) (PEU) material as an alternative to PCL for the generation of an in vitro model of early chondrogenesis. The polymer was successfully printed into 3D constructs displaying adequate substrate stiffness and increased hydrophilicity compared to PCL. Human chondrocytes cultured on the scaffolds exhibited higher cell viability and improved chondrogenic phenotype with upregulation of genes associated with type II collagen and aggrecan synthesis. Bioprinted PEU scaffolds could, therefore, provide a potential platform for the fabrication of bespoke, pro-chondrogenic tissue engineering constructs. |
format | Online Article Text |
id | pubmed-7408263 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-74082632020-08-13 A Preliminary Evaluation of the Pro-Chondrogenic Potential of 3D-Bioprinted Poly(ester Urea) Scaffolds Moxon, Samuel R. Ferreira, Miguel J.S. dos Santos, Patricia Popa, Bogdan Gloria, Antonio Katsarava, Ramaz Tugushi, David Serra, Armenio C. Hooper, Nigel M. Kimber, Susan J. Fonseca, Ana C. Domingos, Marco A. N. Polymers (Basel) Article Degeneration of articular cartilage (AC) is a common healthcare issue that can result in significantly impaired function and mobility for affected patients. The avascular nature of the tissue strongly burdens its regenerative capacity contributing to the development of more serious conditions such as osteoarthritis. Recent advances in bioprinting have prompted the development of alternative tissue engineering therapies for the generation of AC. Particular interest has been dedicated to scaffold-based strategies where 3D substrates are used to guide cellular function and tissue ingrowth. Despite its extensive use in bioprinting, the application of polycaprolactone (PCL) in AC is, however, restricted by properties that inhibit pro-chondrogenic cell phenotypes. This study proposes the use of a new bioprintable poly(ester urea) (PEU) material as an alternative to PCL for the generation of an in vitro model of early chondrogenesis. The polymer was successfully printed into 3D constructs displaying adequate substrate stiffness and increased hydrophilicity compared to PCL. Human chondrocytes cultured on the scaffolds exhibited higher cell viability and improved chondrogenic phenotype with upregulation of genes associated with type II collagen and aggrecan synthesis. Bioprinted PEU scaffolds could, therefore, provide a potential platform for the fabrication of bespoke, pro-chondrogenic tissue engineering constructs. MDPI 2020-06-30 /pmc/articles/PMC7408263/ /pubmed/32630145 http://dx.doi.org/10.3390/polym12071478 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 Moxon, Samuel R. Ferreira, Miguel J.S. dos Santos, Patricia Popa, Bogdan Gloria, Antonio Katsarava, Ramaz Tugushi, David Serra, Armenio C. Hooper, Nigel M. Kimber, Susan J. Fonseca, Ana C. Domingos, Marco A. N. A Preliminary Evaluation of the Pro-Chondrogenic Potential of 3D-Bioprinted Poly(ester Urea) Scaffolds |
title | A Preliminary Evaluation of the Pro-Chondrogenic Potential of 3D-Bioprinted Poly(ester Urea) Scaffolds |
title_full | A Preliminary Evaluation of the Pro-Chondrogenic Potential of 3D-Bioprinted Poly(ester Urea) Scaffolds |
title_fullStr | A Preliminary Evaluation of the Pro-Chondrogenic Potential of 3D-Bioprinted Poly(ester Urea) Scaffolds |
title_full_unstemmed | A Preliminary Evaluation of the Pro-Chondrogenic Potential of 3D-Bioprinted Poly(ester Urea) Scaffolds |
title_short | A Preliminary Evaluation of the Pro-Chondrogenic Potential of 3D-Bioprinted Poly(ester Urea) Scaffolds |
title_sort | preliminary evaluation of the pro-chondrogenic potential of 3d-bioprinted poly(ester urea) scaffolds |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7408263/ https://www.ncbi.nlm.nih.gov/pubmed/32630145 http://dx.doi.org/10.3390/polym12071478 |
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