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Characterization of Polycaprolactone Nanohydroxyapatite Composites with Tunable Degradability Suitable for Indirect Printing

Degradable bone implants are designed to foster the complete regeneration of natural tissue after large-scale loss trauma. Polycaprolactone (PCL) and hydroxyapatite (HA) composites are promising scaffold materials with superior mechanical and osteoinductive properties compared to the single material...

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Autores principales: Doyle, Stephanie E., Henry, Lauren, McGennisken, Ellen, Onofrillo, Carmine, Bella, Claudia Di, Duchi, Serena, O’Connell, Cathal D., Pirogova, Elena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7831941/
https://www.ncbi.nlm.nih.gov/pubmed/33477660
http://dx.doi.org/10.3390/polym13020295
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author Doyle, Stephanie E.
Henry, Lauren
McGennisken, Ellen
Onofrillo, Carmine
Bella, Claudia Di
Duchi, Serena
O’Connell, Cathal D.
Pirogova, Elena
author_facet Doyle, Stephanie E.
Henry, Lauren
McGennisken, Ellen
Onofrillo, Carmine
Bella, Claudia Di
Duchi, Serena
O’Connell, Cathal D.
Pirogova, Elena
author_sort Doyle, Stephanie E.
collection PubMed
description Degradable bone implants are designed to foster the complete regeneration of natural tissue after large-scale loss trauma. Polycaprolactone (PCL) and hydroxyapatite (HA) composites are promising scaffold materials with superior mechanical and osteoinductive properties compared to the single materials. However, producing three-dimensional (3D) structures with high HA content as well as tuneable degradability remains a challenge. To address this issue and create homogeneously distributed PCL-nanoHA (nHA) scaffolds with tuneable degradation rates through both PCL molecular weight and nHA concentration, we conducted a detailed characterisation and comparison of a range of PCL-nHA composites across three molecular weight PCLs (14, 45, and 80 kDa) and with nHA content up to 30% w/w. In general, the addition of nHA results in an increase of viscosity for the PCL-nHA composites but has little effect on their compressive modulus. Importantly, we observe that the addition of nHA increases the rate of degradation compared to PCL alone. We show that the 45 and 80 kDa PCL-nHA groups can be fabricated via indirect 3D printing and have homogenously distributed nHA even after fabrication. Finally, the cytocompatibility of the composite materials is evaluated for the 45 and 80 kDa groups, with the results showing no significant change in cell number compared to the control. In conclusion, our analyses unveil several features that are crucial for processing the composite material into a tissue engineered implant.
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spelling pubmed-78319412021-01-26 Characterization of Polycaprolactone Nanohydroxyapatite Composites with Tunable Degradability Suitable for Indirect Printing Doyle, Stephanie E. Henry, Lauren McGennisken, Ellen Onofrillo, Carmine Bella, Claudia Di Duchi, Serena O’Connell, Cathal D. Pirogova, Elena Polymers (Basel) Article Degradable bone implants are designed to foster the complete regeneration of natural tissue after large-scale loss trauma. Polycaprolactone (PCL) and hydroxyapatite (HA) composites are promising scaffold materials with superior mechanical and osteoinductive properties compared to the single materials. However, producing three-dimensional (3D) structures with high HA content as well as tuneable degradability remains a challenge. To address this issue and create homogeneously distributed PCL-nanoHA (nHA) scaffolds with tuneable degradation rates through both PCL molecular weight and nHA concentration, we conducted a detailed characterisation and comparison of a range of PCL-nHA composites across three molecular weight PCLs (14, 45, and 80 kDa) and with nHA content up to 30% w/w. In general, the addition of nHA results in an increase of viscosity for the PCL-nHA composites but has little effect on their compressive modulus. Importantly, we observe that the addition of nHA increases the rate of degradation compared to PCL alone. We show that the 45 and 80 kDa PCL-nHA groups can be fabricated via indirect 3D printing and have homogenously distributed nHA even after fabrication. Finally, the cytocompatibility of the composite materials is evaluated for the 45 and 80 kDa groups, with the results showing no significant change in cell number compared to the control. In conclusion, our analyses unveil several features that are crucial for processing the composite material into a tissue engineered implant. MDPI 2021-01-18 /pmc/articles/PMC7831941/ /pubmed/33477660 http://dx.doi.org/10.3390/polym13020295 Text en © 2021 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
Doyle, Stephanie E.
Henry, Lauren
McGennisken, Ellen
Onofrillo, Carmine
Bella, Claudia Di
Duchi, Serena
O’Connell, Cathal D.
Pirogova, Elena
Characterization of Polycaprolactone Nanohydroxyapatite Composites with Tunable Degradability Suitable for Indirect Printing
title Characterization of Polycaprolactone Nanohydroxyapatite Composites with Tunable Degradability Suitable for Indirect Printing
title_full Characterization of Polycaprolactone Nanohydroxyapatite Composites with Tunable Degradability Suitable for Indirect Printing
title_fullStr Characterization of Polycaprolactone Nanohydroxyapatite Composites with Tunable Degradability Suitable for Indirect Printing
title_full_unstemmed Characterization of Polycaprolactone Nanohydroxyapatite Composites with Tunable Degradability Suitable for Indirect Printing
title_short Characterization of Polycaprolactone Nanohydroxyapatite Composites with Tunable Degradability Suitable for Indirect Printing
title_sort characterization of polycaprolactone nanohydroxyapatite composites with tunable degradability suitable for indirect printing
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7831941/
https://www.ncbi.nlm.nih.gov/pubmed/33477660
http://dx.doi.org/10.3390/polym13020295
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