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The Rheology and Printability of Cartilage Matrix-Only Biomaterials

The potential chondroinductivity from cartilage matrix makes it promising for cartilage repair; however, cartilage matrix-based hydrogels developed thus far have failed to match the mechanical performance of native cartilage or be bioprinted without adding polymers for reinforcement. There is a need...

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Autores principales: Kiyotake, Emi A., Cheng, Michael E., Thomas, Emily E., Detamore, Michael S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9220845/
https://www.ncbi.nlm.nih.gov/pubmed/35740971
http://dx.doi.org/10.3390/biom12060846
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author Kiyotake, Emi A.
Cheng, Michael E.
Thomas, Emily E.
Detamore, Michael S.
author_facet Kiyotake, Emi A.
Cheng, Michael E.
Thomas, Emily E.
Detamore, Michael S.
author_sort Kiyotake, Emi A.
collection PubMed
description The potential chondroinductivity from cartilage matrix makes it promising for cartilage repair; however, cartilage matrix-based hydrogels developed thus far have failed to match the mechanical performance of native cartilage or be bioprinted without adding polymers for reinforcement. There is a need for cartilage matrix-based hydrogels with robust mechanical performance and paste-like precursor rheology for bioprinting/enhanced surgical placement. In the current study, our goals were to increase hydrogel stiffness and develop the paste-like precursor/printability of our methacryl-modified solubilized and devitalized cartilage (MeSDVC) hydrogels. We compared two methacryloylating reagents, methacrylic anhydride (MA) and glycidyl methacrylate (GM), and varied the molar excess (ME) of MA from 2 to 20. The MA-modified MeSDVCs had greater methacryloylation than GM-modified MeSDVC (20 ME). While GM and most of the MA hydrogel precursors exhibited paste-like rheology, the 2 ME MA and GM MeSDVCs had the best printability (i.e., shape fidelity, filament collapse). After crosslinking, the 2 ME MA MeSDVC had the highest stiffness (1.55 ± 0.23 MPa), approaching the modulus of native cartilage, and supported the viability/adhesion of seeded cells for 15 days. Overall, the MA (2 ME) improved methacryloylation, hydrogel stiffness, and printability, resulting in a stand-alone MeSDVC printable biomaterial. The MeSDVC has potential as a future bioink and has future clinical relevance for cartilage repair.
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spelling pubmed-92208452022-06-24 The Rheology and Printability of Cartilage Matrix-Only Biomaterials Kiyotake, Emi A. Cheng, Michael E. Thomas, Emily E. Detamore, Michael S. Biomolecules Article The potential chondroinductivity from cartilage matrix makes it promising for cartilage repair; however, cartilage matrix-based hydrogels developed thus far have failed to match the mechanical performance of native cartilage or be bioprinted without adding polymers for reinforcement. There is a need for cartilage matrix-based hydrogels with robust mechanical performance and paste-like precursor rheology for bioprinting/enhanced surgical placement. In the current study, our goals were to increase hydrogel stiffness and develop the paste-like precursor/printability of our methacryl-modified solubilized and devitalized cartilage (MeSDVC) hydrogels. We compared two methacryloylating reagents, methacrylic anhydride (MA) and glycidyl methacrylate (GM), and varied the molar excess (ME) of MA from 2 to 20. The MA-modified MeSDVCs had greater methacryloylation than GM-modified MeSDVC (20 ME). While GM and most of the MA hydrogel precursors exhibited paste-like rheology, the 2 ME MA and GM MeSDVCs had the best printability (i.e., shape fidelity, filament collapse). After crosslinking, the 2 ME MA MeSDVC had the highest stiffness (1.55 ± 0.23 MPa), approaching the modulus of native cartilage, and supported the viability/adhesion of seeded cells for 15 days. Overall, the MA (2 ME) improved methacryloylation, hydrogel stiffness, and printability, resulting in a stand-alone MeSDVC printable biomaterial. The MeSDVC has potential as a future bioink and has future clinical relevance for cartilage repair. MDPI 2022-06-17 /pmc/articles/PMC9220845/ /pubmed/35740971 http://dx.doi.org/10.3390/biom12060846 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kiyotake, Emi A.
Cheng, Michael E.
Thomas, Emily E.
Detamore, Michael S.
The Rheology and Printability of Cartilage Matrix-Only Biomaterials
title The Rheology and Printability of Cartilage Matrix-Only Biomaterials
title_full The Rheology and Printability of Cartilage Matrix-Only Biomaterials
title_fullStr The Rheology and Printability of Cartilage Matrix-Only Biomaterials
title_full_unstemmed The Rheology and Printability of Cartilage Matrix-Only Biomaterials
title_short The Rheology and Printability of Cartilage Matrix-Only Biomaterials
title_sort rheology and printability of cartilage matrix-only biomaterials
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9220845/
https://www.ncbi.nlm.nih.gov/pubmed/35740971
http://dx.doi.org/10.3390/biom12060846
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