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Gelatin-modified 3D printed PGS elastic hierarchical porous scaffold for cartilage regeneration
Regenerative cartilage replacements are increasingly required in clinical settings for various defect repairs, including bronchial cartilage deficiency, articular cartilage injury, and microtia reconstruction. Poly (glycerol sebacate) (PGS) is a widely used bioelastomer that has been developed for v...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AIP Publishing LLC
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10404141/ https://www.ncbi.nlm.nih.gov/pubmed/37547670 http://dx.doi.org/10.1063/5.0152151 |
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author | Wang, Sinan Chen, Hongying Huang, Jinyi Shen, Sisi Tang, Zhengya Tan, Xiaoyan Lei, Dong Zhou, Guangdong |
author_facet | Wang, Sinan Chen, Hongying Huang, Jinyi Shen, Sisi Tang, Zhengya Tan, Xiaoyan Lei, Dong Zhou, Guangdong |
author_sort | Wang, Sinan |
collection | PubMed |
description | Regenerative cartilage replacements are increasingly required in clinical settings for various defect repairs, including bronchial cartilage deficiency, articular cartilage injury, and microtia reconstruction. Poly (glycerol sebacate) (PGS) is a widely used bioelastomer that has been developed for various regenerative medicine applications because of its excellent elasticity, biodegradability, and biocompatibility. However, because of inadequate active groups, strong hydrophobicity, and limited ink extrusion accuracy, 3D printed PGS scaffolds may cause insufficient bioactivity, inefficient cell inoculation, and inconsistent cellular composition, which seriously hinders its further cartilage regenerative application. Here, we combined 3D printed PGS frameworks with an encapsulated gelatin hydrogel to fabricate a PGS@Gel composite scaffold. PGS@Gel scaffolds have a controllable porous microstructure, with suitable pore sizes and enhanced hydrophilia, which could significantly promote the cells' penetration and adhesion for efficient chondrocyte inoculation. Furthermore, the outstanding elasticity and fatigue durability of the PGS framework enabled the regenerated cartilage built by the PGS@Gel scaffolds to resist the dynamic in vivo environment and maintain its original morphology. Importantly, PGS@Gel scaffolds increased the rate of cartilage regeneration concurrent with scaffold degradation. The scaffold was gradually degraded and integrated to form uniform, dense, and mature regenerated cartilage tissue with little scaffold residue. |
format | Online Article Text |
id | pubmed-10404141 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | AIP Publishing LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-104041412023-08-06 Gelatin-modified 3D printed PGS elastic hierarchical porous scaffold for cartilage regeneration Wang, Sinan Chen, Hongying Huang, Jinyi Shen, Sisi Tang, Zhengya Tan, Xiaoyan Lei, Dong Zhou, Guangdong APL Bioeng Articles Regenerative cartilage replacements are increasingly required in clinical settings for various defect repairs, including bronchial cartilage deficiency, articular cartilage injury, and microtia reconstruction. Poly (glycerol sebacate) (PGS) is a widely used bioelastomer that has been developed for various regenerative medicine applications because of its excellent elasticity, biodegradability, and biocompatibility. However, because of inadequate active groups, strong hydrophobicity, and limited ink extrusion accuracy, 3D printed PGS scaffolds may cause insufficient bioactivity, inefficient cell inoculation, and inconsistent cellular composition, which seriously hinders its further cartilage regenerative application. Here, we combined 3D printed PGS frameworks with an encapsulated gelatin hydrogel to fabricate a PGS@Gel composite scaffold. PGS@Gel scaffolds have a controllable porous microstructure, with suitable pore sizes and enhanced hydrophilia, which could significantly promote the cells' penetration and adhesion for efficient chondrocyte inoculation. Furthermore, the outstanding elasticity and fatigue durability of the PGS framework enabled the regenerated cartilage built by the PGS@Gel scaffolds to resist the dynamic in vivo environment and maintain its original morphology. Importantly, PGS@Gel scaffolds increased the rate of cartilage regeneration concurrent with scaffold degradation. The scaffold was gradually degraded and integrated to form uniform, dense, and mature regenerated cartilage tissue with little scaffold residue. AIP Publishing LLC 2023-08-04 /pmc/articles/PMC10404141/ /pubmed/37547670 http://dx.doi.org/10.1063/5.0152151 Text en © 2023 Author(s). https://creativecommons.org/licenses/by/4.0/All article content, except where otherwise noted, is licensed under a Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ). |
spellingShingle | Articles Wang, Sinan Chen, Hongying Huang, Jinyi Shen, Sisi Tang, Zhengya Tan, Xiaoyan Lei, Dong Zhou, Guangdong Gelatin-modified 3D printed PGS elastic hierarchical porous scaffold for cartilage regeneration |
title | Gelatin-modified 3D printed PGS elastic hierarchical porous scaffold for cartilage regeneration |
title_full | Gelatin-modified 3D printed PGS elastic hierarchical porous scaffold for cartilage regeneration |
title_fullStr | Gelatin-modified 3D printed PGS elastic hierarchical porous scaffold for cartilage regeneration |
title_full_unstemmed | Gelatin-modified 3D printed PGS elastic hierarchical porous scaffold for cartilage regeneration |
title_short | Gelatin-modified 3D printed PGS elastic hierarchical porous scaffold for cartilage regeneration |
title_sort | gelatin-modified 3d printed pgs elastic hierarchical porous scaffold for cartilage regeneration |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10404141/ https://www.ncbi.nlm.nih.gov/pubmed/37547670 http://dx.doi.org/10.1063/5.0152151 |
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