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Formulation of a covalently bonded hydroxyapatite and poly(ether ether ketone) composite
Spinal fusion devices can be fabricated from composites based on combining hydroxyapatite and poly(ether ether ketone) phases. These implants serve as load-bearing scaffolds for the formation of new bone tissue between adjacent vertebrae. In this work, we report a novel approach to covalently bond h...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6299303/ https://www.ncbi.nlm.nih.gov/pubmed/30574291 http://dx.doi.org/10.1177/2041731418815570 |
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author | Hughes, Erik AB Parkes, Andrew Williams, Richard L Jenkins, Mike J Grover, Liam M |
author_facet | Hughes, Erik AB Parkes, Andrew Williams, Richard L Jenkins, Mike J Grover, Liam M |
author_sort | Hughes, Erik AB |
collection | PubMed |
description | Spinal fusion devices can be fabricated from composites based on combining hydroxyapatite and poly(ether ether ketone) phases. These implants serve as load-bearing scaffolds for the formation of new bone tissue between adjacent vertebrae. In this work, we report a novel approach to covalently bond hydroxyapatite and poly(ether ether ketone) to produce a novel composite formulation with enhanced interfacial adhesion between phases. Compared to non-linked composites (HA_PEEK), covalently linked composites (HA_L_PEEK), loaded with 1.25 vol% hydroxyapatite, possessed a greater mean flexural strength (170 ± 5.4 vs 171.7 ± 14.8 MPa (mean ± SD)) and modulus (4.8 ± 0.2 vs 5.0 ± 0.3 GPa (mean ± SD)). Although the mechanical properties were not found to be significantly different (p > 0.05), PEEK_L_HA contained substantially larger hydroxyapatite inclusions (100–1000 µm) compared to HA_PEEK (50–200 µm), due to the inherently agglomerative nature of the covalently bonded hydroxyapatite and poly(ether ether ketone) additive. Larger inclusions would expectedly weaken the HA_L_PEEK composite; however, there is no significant difference between the flexural modulus of poly(ether ether ketone) with respect to HA_L_PEEK (p = 0.13). In addition, the flexural modulus of HA_PEEK is significantly lower compared to poly(ether ether ketone) (p = 0.03). Ultimately, covalent linking reduces hydroxyapatite particulate de-bonding from the polymeric matrix and inhibits micro-crack development, culminating in enhanced transfer of stiffness between hydroxyapatite and poly(ether ether ketone) under loading. |
format | Online Article Text |
id | pubmed-6299303 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-62993032018-12-20 Formulation of a covalently bonded hydroxyapatite and poly(ether ether ketone) composite Hughes, Erik AB Parkes, Andrew Williams, Richard L Jenkins, Mike J Grover, Liam M J Tissue Eng Acellular Approaches for Regenerative Medicine: Driving Biology without the Cell Spinal fusion devices can be fabricated from composites based on combining hydroxyapatite and poly(ether ether ketone) phases. These implants serve as load-bearing scaffolds for the formation of new bone tissue between adjacent vertebrae. In this work, we report a novel approach to covalently bond hydroxyapatite and poly(ether ether ketone) to produce a novel composite formulation with enhanced interfacial adhesion between phases. Compared to non-linked composites (HA_PEEK), covalently linked composites (HA_L_PEEK), loaded with 1.25 vol% hydroxyapatite, possessed a greater mean flexural strength (170 ± 5.4 vs 171.7 ± 14.8 MPa (mean ± SD)) and modulus (4.8 ± 0.2 vs 5.0 ± 0.3 GPa (mean ± SD)). Although the mechanical properties were not found to be significantly different (p > 0.05), PEEK_L_HA contained substantially larger hydroxyapatite inclusions (100–1000 µm) compared to HA_PEEK (50–200 µm), due to the inherently agglomerative nature of the covalently bonded hydroxyapatite and poly(ether ether ketone) additive. Larger inclusions would expectedly weaken the HA_L_PEEK composite; however, there is no significant difference between the flexural modulus of poly(ether ether ketone) with respect to HA_L_PEEK (p = 0.13). In addition, the flexural modulus of HA_PEEK is significantly lower compared to poly(ether ether ketone) (p = 0.03). Ultimately, covalent linking reduces hydroxyapatite particulate de-bonding from the polymeric matrix and inhibits micro-crack development, culminating in enhanced transfer of stiffness between hydroxyapatite and poly(ether ether ketone) under loading. SAGE Publications 2018-12-17 /pmc/articles/PMC6299303/ /pubmed/30574291 http://dx.doi.org/10.1177/2041731418815570 Text en © The Author(s) 2018 http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution 4.0 License (http://www.creativecommons.org/licenses/by/4.0/) which permits any use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Acellular Approaches for Regenerative Medicine: Driving Biology without the Cell Hughes, Erik AB Parkes, Andrew Williams, Richard L Jenkins, Mike J Grover, Liam M Formulation of a covalently bonded hydroxyapatite and poly(ether ether ketone) composite |
title | Formulation of a covalently bonded hydroxyapatite and poly(ether ether ketone) composite |
title_full | Formulation of a covalently bonded hydroxyapatite and poly(ether ether ketone) composite |
title_fullStr | Formulation of a covalently bonded hydroxyapatite and poly(ether ether ketone) composite |
title_full_unstemmed | Formulation of a covalently bonded hydroxyapatite and poly(ether ether ketone) composite |
title_short | Formulation of a covalently bonded hydroxyapatite and poly(ether ether ketone) composite |
title_sort | formulation of a covalently bonded hydroxyapatite and poly(ether ether ketone) composite |
topic | Acellular Approaches for Regenerative Medicine: Driving Biology without the Cell |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6299303/ https://www.ncbi.nlm.nih.gov/pubmed/30574291 http://dx.doi.org/10.1177/2041731418815570 |
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