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Bisphosphonate nanoclay edge-site interactions facilitate hydrogel self-assembly and sustained growth factor localization
Nanoclays have generated interest in biomaterial design for their ability to enhance the mechanics of polymeric materials and impart biological function. As well as their utility as physical cross-linkers, clays have been explored for sustained localization of biomolecules to promote in vivo tissue...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7069965/ https://www.ncbi.nlm.nih.gov/pubmed/32170076 http://dx.doi.org/10.1038/s41467-020-15152-9 |
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author | Kim, Yang-Hee Yang, Xia Shi, Liyang Lanham, Stuart A. Hilborn, Jons Oreffo, Richard O. C. Ossipov, Dmitri Dawson, Jonathan I. |
author_facet | Kim, Yang-Hee Yang, Xia Shi, Liyang Lanham, Stuart A. Hilborn, Jons Oreffo, Richard O. C. Ossipov, Dmitri Dawson, Jonathan I. |
author_sort | Kim, Yang-Hee |
collection | PubMed |
description | Nanoclays have generated interest in biomaterial design for their ability to enhance the mechanics of polymeric materials and impart biological function. As well as their utility as physical cross-linkers, clays have been explored for sustained localization of biomolecules to promote in vivo tissue regeneration. To date, both biomolecule-clay and polymer-clay nanocomposite strategies have utilised the negatively charged clay particle surface. As such, biomolecule-clay and polymer-clay interactions are set in competition, potentially limiting the functional enhancements achieved. Here, we apply specific bisphosphonate interactions with the positively charged clay particle edge to develop self-assembling hydrogels and functionalized clay nanoparticles with preserved surface exchange capacity. Low concentrations of nanoclay are applied to cross-link hyaluronic acid polymers derivatised with a pendant bisphosphonate to generate hydrogels with enhanced mechanical properties and preserved protein binding able to sustain, for over six weeks in vivo, the localized activity of the clinically licensed growth factor BMP-2. |
format | Online Article Text |
id | pubmed-7069965 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-70699652020-03-18 Bisphosphonate nanoclay edge-site interactions facilitate hydrogel self-assembly and sustained growth factor localization Kim, Yang-Hee Yang, Xia Shi, Liyang Lanham, Stuart A. Hilborn, Jons Oreffo, Richard O. C. Ossipov, Dmitri Dawson, Jonathan I. Nat Commun Article Nanoclays have generated interest in biomaterial design for their ability to enhance the mechanics of polymeric materials and impart biological function. As well as their utility as physical cross-linkers, clays have been explored for sustained localization of biomolecules to promote in vivo tissue regeneration. To date, both biomolecule-clay and polymer-clay nanocomposite strategies have utilised the negatively charged clay particle surface. As such, biomolecule-clay and polymer-clay interactions are set in competition, potentially limiting the functional enhancements achieved. Here, we apply specific bisphosphonate interactions with the positively charged clay particle edge to develop self-assembling hydrogels and functionalized clay nanoparticles with preserved surface exchange capacity. Low concentrations of nanoclay are applied to cross-link hyaluronic acid polymers derivatised with a pendant bisphosphonate to generate hydrogels with enhanced mechanical properties and preserved protein binding able to sustain, for over six weeks in vivo, the localized activity of the clinically licensed growth factor BMP-2. Nature Publishing Group UK 2020-03-13 /pmc/articles/PMC7069965/ /pubmed/32170076 http://dx.doi.org/10.1038/s41467-020-15152-9 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Kim, Yang-Hee Yang, Xia Shi, Liyang Lanham, Stuart A. Hilborn, Jons Oreffo, Richard O. C. Ossipov, Dmitri Dawson, Jonathan I. Bisphosphonate nanoclay edge-site interactions facilitate hydrogel self-assembly and sustained growth factor localization |
title | Bisphosphonate nanoclay edge-site interactions facilitate hydrogel self-assembly and sustained growth factor localization |
title_full | Bisphosphonate nanoclay edge-site interactions facilitate hydrogel self-assembly and sustained growth factor localization |
title_fullStr | Bisphosphonate nanoclay edge-site interactions facilitate hydrogel self-assembly and sustained growth factor localization |
title_full_unstemmed | Bisphosphonate nanoclay edge-site interactions facilitate hydrogel self-assembly and sustained growth factor localization |
title_short | Bisphosphonate nanoclay edge-site interactions facilitate hydrogel self-assembly and sustained growth factor localization |
title_sort | bisphosphonate nanoclay edge-site interactions facilitate hydrogel self-assembly and sustained growth factor localization |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7069965/ https://www.ncbi.nlm.nih.gov/pubmed/32170076 http://dx.doi.org/10.1038/s41467-020-15152-9 |
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