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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
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.
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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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