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Peptide:glycosaminoglycan hybrid hydrogels as an injectable intervention for spinal disc degeneration
Degeneration of the spinal discs is a major cause of back pain. During the degeneration process, there is a loss of glycosaminoglycans (GAGs) from the proteoglycan-rich gel in the disc's nucleus, which adversely alters biomechanical performance. Current surgical treatments for back pain are hig...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4920072/ https://www.ncbi.nlm.nih.gov/pubmed/27429755 http://dx.doi.org/10.1039/c6tb00121a |
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author | Miles, D. E. Mitchell, E. A. Kapur, N. Beales, P. A. Wilcox, R. K. |
author_facet | Miles, D. E. Mitchell, E. A. Kapur, N. Beales, P. A. Wilcox, R. K. |
author_sort | Miles, D. E. |
collection | PubMed |
description | Degeneration of the spinal discs is a major cause of back pain. During the degeneration process, there is a loss of glycosaminoglycans (GAGs) from the proteoglycan-rich gel in the disc's nucleus, which adversely alters biomechanical performance. Current surgical treatments for back pain are highly invasive and have low success rates; there is an urgent need for minimally-invasive approaches that restore the physiological mechanics of the spine. Here we present an injectable peptide:GAG hydrogel that rapidly self-assembles in situ and restores the mechanics of denucleated intervertebral discs. It forms a gel with comparable mechanical properties to the native tissue within seconds to minutes depending on the peptide chosen. Unlike other biomaterials that have been proposed for this purpose, these hybrid hydrogels can be injected through a very narrow 25 G gauge needle, minimising damage to the surrounding soft tissue, and they mimic the ability of the natural tissue to draw in water by incorporating GAGs. Furthermore, the GAGs enhance the gelation kinetics and thermodynamic stability of peptide hydrogels, significantly reducing effusion of injected material from the intervertebral disc (GAG leakage of 8 ± 3% after 24 h when peptide present, compared to 39 ± 3% when no peptide present). In an ex vivo model, we demonstrate that the hydrogels can restore the compressive stiffness of denucleated bovine intervertebral discs. Compellingly, this novel biomaterial has the potential to transform the clinical treatment of back pain by resolving current surgical challenges, thus improving patient quality of life. |
format | Online Article Text |
id | pubmed-4920072 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-49200722016-07-15 Peptide:glycosaminoglycan hybrid hydrogels as an injectable intervention for spinal disc degeneration Miles, D. E. Mitchell, E. A. Kapur, N. Beales, P. A. Wilcox, R. K. J Mater Chem B Mater Biol Med Chemistry Degeneration of the spinal discs is a major cause of back pain. During the degeneration process, there is a loss of glycosaminoglycans (GAGs) from the proteoglycan-rich gel in the disc's nucleus, which adversely alters biomechanical performance. Current surgical treatments for back pain are highly invasive and have low success rates; there is an urgent need for minimally-invasive approaches that restore the physiological mechanics of the spine. Here we present an injectable peptide:GAG hydrogel that rapidly self-assembles in situ and restores the mechanics of denucleated intervertebral discs. It forms a gel with comparable mechanical properties to the native tissue within seconds to minutes depending on the peptide chosen. Unlike other biomaterials that have been proposed for this purpose, these hybrid hydrogels can be injected through a very narrow 25 G gauge needle, minimising damage to the surrounding soft tissue, and they mimic the ability of the natural tissue to draw in water by incorporating GAGs. Furthermore, the GAGs enhance the gelation kinetics and thermodynamic stability of peptide hydrogels, significantly reducing effusion of injected material from the intervertebral disc (GAG leakage of 8 ± 3% after 24 h when peptide present, compared to 39 ± 3% when no peptide present). In an ex vivo model, we demonstrate that the hydrogels can restore the compressive stiffness of denucleated bovine intervertebral discs. Compellingly, this novel biomaterial has the potential to transform the clinical treatment of back pain by resolving current surgical challenges, thus improving patient quality of life. Royal Society of Chemistry 2016-05-11 2016-05-21 /pmc/articles/PMC4920072/ /pubmed/27429755 http://dx.doi.org/10.1039/c6tb00121a Text en This journal is © The Royal Society of Chemistry 2016 http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution 3.0 Unported License (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Chemistry Miles, D. E. Mitchell, E. A. Kapur, N. Beales, P. A. Wilcox, R. K. Peptide:glycosaminoglycan hybrid hydrogels as an injectable intervention for spinal disc degeneration |
title | Peptide:glycosaminoglycan hybrid hydrogels as an injectable intervention for spinal disc degeneration
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title_full | Peptide:glycosaminoglycan hybrid hydrogels as an injectable intervention for spinal disc degeneration
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title_fullStr | Peptide:glycosaminoglycan hybrid hydrogels as an injectable intervention for spinal disc degeneration
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title_full_unstemmed | Peptide:glycosaminoglycan hybrid hydrogels as an injectable intervention for spinal disc degeneration
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title_short | Peptide:glycosaminoglycan hybrid hydrogels as an injectable intervention for spinal disc degeneration
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title_sort | peptide:glycosaminoglycan hybrid hydrogels as an injectable intervention for spinal disc degeneration |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4920072/ https://www.ncbi.nlm.nih.gov/pubmed/27429755 http://dx.doi.org/10.1039/c6tb00121a |
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