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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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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. |
format | Online Article Text |
id | pubmed-9220845 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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