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PEEK and Hyaluronan-Based 3D Printed Structures: Promising Combination to Improve Bone Regeneration
Hybrid bone substitute made up of a 3D printed polyetheretherketone (PEEK) scaffold coated with methacrylated hyaluronic acid (MeHA)-hydroxyapatite (HAp) hydrogel is the objective of the present work. Development and characterization of the scaffold and of the MeHA-HAp after its infiltration and UV...
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/PMC9787780/ https://www.ncbi.nlm.nih.gov/pubmed/36557882 http://dx.doi.org/10.3390/molecules27248749 |
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author | Ferroni, Letizia D’Amora, Ugo Leo, Sara Tremoli, Elena Raucci, Maria Grazia Ronca, Alfredo Ambrosio, Luigi Zavan, Barbara |
author_facet | Ferroni, Letizia D’Amora, Ugo Leo, Sara Tremoli, Elena Raucci, Maria Grazia Ronca, Alfredo Ambrosio, Luigi Zavan, Barbara |
author_sort | Ferroni, Letizia |
collection | PubMed |
description | Hybrid bone substitute made up of a 3D printed polyetheretherketone (PEEK) scaffold coated with methacrylated hyaluronic acid (MeHA)-hydroxyapatite (HAp) hydrogel is the objective of the present work. Development and characterization of the scaffold and of the MeHA-HAp after its infiltration and UV photocrosslinking have been followed by analyses of its biological properties using human mesenchymal stem cells (MSCs). Interconnected porous PEEK matrices were produced by fused deposition modeling (FDM) characterized by a reticular pattern with 0°/90° raster orientation and square pores. In parallel, a MeHA-HAp slurry has been synthesized and infiltrated in the PEEK scaffolds. The mechanical properties of the coated and pure PEEK scaffold have been evaluated, showing that the inclusion of MeHA-HAp into the lattice geometry did not significantly change the strength of the PEEK structure with Young’s modulus of 1034.9 ± 126.1 MPa and 1020.0 ± 63.7 MPa for PEEK and PEEK-MeHA-HAp scaffolds, respectively. Human MSCs were seeded on bare and coated scaffolds and cultured for up to 28 days to determine the adhesion, proliferation, migration and osteogenic differentiation. In vitro results showed that the MeHA-HAp coating promotes MSCs adhesion and proliferation and contributes to osteogenic differentiation and extracellular matrix mineralization. This study provides an efficient solution for the development of a scaffold combining the great mechanical performances of PEEK with the bioactive properties of MeHA and HAp, having high potential for translational clinical applications. |
format | Online Article Text |
id | pubmed-9787780 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-97877802022-12-24 PEEK and Hyaluronan-Based 3D Printed Structures: Promising Combination to Improve Bone Regeneration Ferroni, Letizia D’Amora, Ugo Leo, Sara Tremoli, Elena Raucci, Maria Grazia Ronca, Alfredo Ambrosio, Luigi Zavan, Barbara Molecules Article Hybrid bone substitute made up of a 3D printed polyetheretherketone (PEEK) scaffold coated with methacrylated hyaluronic acid (MeHA)-hydroxyapatite (HAp) hydrogel is the objective of the present work. Development and characterization of the scaffold and of the MeHA-HAp after its infiltration and UV photocrosslinking have been followed by analyses of its biological properties using human mesenchymal stem cells (MSCs). Interconnected porous PEEK matrices were produced by fused deposition modeling (FDM) characterized by a reticular pattern with 0°/90° raster orientation and square pores. In parallel, a MeHA-HAp slurry has been synthesized and infiltrated in the PEEK scaffolds. The mechanical properties of the coated and pure PEEK scaffold have been evaluated, showing that the inclusion of MeHA-HAp into the lattice geometry did not significantly change the strength of the PEEK structure with Young’s modulus of 1034.9 ± 126.1 MPa and 1020.0 ± 63.7 MPa for PEEK and PEEK-MeHA-HAp scaffolds, respectively. Human MSCs were seeded on bare and coated scaffolds and cultured for up to 28 days to determine the adhesion, proliferation, migration and osteogenic differentiation. In vitro results showed that the MeHA-HAp coating promotes MSCs adhesion and proliferation and contributes to osteogenic differentiation and extracellular matrix mineralization. This study provides an efficient solution for the development of a scaffold combining the great mechanical performances of PEEK with the bioactive properties of MeHA and HAp, having high potential for translational clinical applications. MDPI 2022-12-09 /pmc/articles/PMC9787780/ /pubmed/36557882 http://dx.doi.org/10.3390/molecules27248749 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 Ferroni, Letizia D’Amora, Ugo Leo, Sara Tremoli, Elena Raucci, Maria Grazia Ronca, Alfredo Ambrosio, Luigi Zavan, Barbara PEEK and Hyaluronan-Based 3D Printed Structures: Promising Combination to Improve Bone Regeneration |
title | PEEK and Hyaluronan-Based 3D Printed Structures: Promising Combination to Improve Bone Regeneration |
title_full | PEEK and Hyaluronan-Based 3D Printed Structures: Promising Combination to Improve Bone Regeneration |
title_fullStr | PEEK and Hyaluronan-Based 3D Printed Structures: Promising Combination to Improve Bone Regeneration |
title_full_unstemmed | PEEK and Hyaluronan-Based 3D Printed Structures: Promising Combination to Improve Bone Regeneration |
title_short | PEEK and Hyaluronan-Based 3D Printed Structures: Promising Combination to Improve Bone Regeneration |
title_sort | peek and hyaluronan-based 3d printed structures: promising combination to improve bone regeneration |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9787780/ https://www.ncbi.nlm.nih.gov/pubmed/36557882 http://dx.doi.org/10.3390/molecules27248749 |
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