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Controlled biodegradation of magnesium alloy in physiological environment by metal organic framework nanocomposite coatings

Magnesium-based implants (MBIs) have recently attracted great attention in bone regeneration due to elastic modulus similar to bone. Nevertheless, the degradation rate and hydrogen release of MBIs in the body have to be tackled for practical applications. In the present study, we present a metal–org...

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Autores principales: Khalili, Mohammad Amin, Tamjid, Elnaz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8060305/
https://www.ncbi.nlm.nih.gov/pubmed/33883594
http://dx.doi.org/10.1038/s41598-021-87783-x
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author Khalili, Mohammad Amin
Tamjid, Elnaz
author_facet Khalili, Mohammad Amin
Tamjid, Elnaz
author_sort Khalili, Mohammad Amin
collection PubMed
description Magnesium-based implants (MBIs) have recently attracted great attention in bone regeneration due to elastic modulus similar to bone. Nevertheless, the degradation rate and hydrogen release of MBIs in the body have to be tackled for practical applications. In the present study, we present a metal–organic framework (MOF) nanoplates to reduce the degradation rate of AZ91 magnesium alloy. Zeolitic imidazolate frameworks (ZIF-8) with a specific surface area of 1789 m(2) g(−1) were prepared by solvothermal methods, and after dispersion in a chitosan solution (10% w/w), the suspension was electrospun on the surface of AZ91 alloy. Studying the degradation rate in simulated body fluid (SBF) by electrochemical analysis including potentiodynamic polarization and electrochemical impedance spectroscopy reveals that the degradation rate of the surface-modified implants decreases by ~ 80% as compared with the unmodified specimens. The reduced alkalization of the physiological environment and hydrogen release due to the implant degradation are shown. In vitro studies by fibroblasts and MG63 osteosarcoma cells exhibit improved cell adhesion and viability. The mechanisms behind the improved degradation resistance and enhanced bioactivity are presented and discussed. Surface modification of MBIs by MOF-chitosan coatings is a promising strategy to control the biodegradation of magnesium implants for bone regeneration.
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spelling pubmed-80603052021-04-22 Controlled biodegradation of magnesium alloy in physiological environment by metal organic framework nanocomposite coatings Khalili, Mohammad Amin Tamjid, Elnaz Sci Rep Article Magnesium-based implants (MBIs) have recently attracted great attention in bone regeneration due to elastic modulus similar to bone. Nevertheless, the degradation rate and hydrogen release of MBIs in the body have to be tackled for practical applications. In the present study, we present a metal–organic framework (MOF) nanoplates to reduce the degradation rate of AZ91 magnesium alloy. Zeolitic imidazolate frameworks (ZIF-8) with a specific surface area of 1789 m(2) g(−1) were prepared by solvothermal methods, and after dispersion in a chitosan solution (10% w/w), the suspension was electrospun on the surface of AZ91 alloy. Studying the degradation rate in simulated body fluid (SBF) by electrochemical analysis including potentiodynamic polarization and electrochemical impedance spectroscopy reveals that the degradation rate of the surface-modified implants decreases by ~ 80% as compared with the unmodified specimens. The reduced alkalization of the physiological environment and hydrogen release due to the implant degradation are shown. In vitro studies by fibroblasts and MG63 osteosarcoma cells exhibit improved cell adhesion and viability. The mechanisms behind the improved degradation resistance and enhanced bioactivity are presented and discussed. Surface modification of MBIs by MOF-chitosan coatings is a promising strategy to control the biodegradation of magnesium implants for bone regeneration. Nature Publishing Group UK 2021-04-21 /pmc/articles/PMC8060305/ /pubmed/33883594 http://dx.doi.org/10.1038/s41598-021-87783-x Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Khalili, Mohammad Amin
Tamjid, Elnaz
Controlled biodegradation of magnesium alloy in physiological environment by metal organic framework nanocomposite coatings
title Controlled biodegradation of magnesium alloy in physiological environment by metal organic framework nanocomposite coatings
title_full Controlled biodegradation of magnesium alloy in physiological environment by metal organic framework nanocomposite coatings
title_fullStr Controlled biodegradation of magnesium alloy in physiological environment by metal organic framework nanocomposite coatings
title_full_unstemmed Controlled biodegradation of magnesium alloy in physiological environment by metal organic framework nanocomposite coatings
title_short Controlled biodegradation of magnesium alloy in physiological environment by metal organic framework nanocomposite coatings
title_sort controlled biodegradation of magnesium alloy in physiological environment by metal organic framework nanocomposite coatings
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8060305/
https://www.ncbi.nlm.nih.gov/pubmed/33883594
http://dx.doi.org/10.1038/s41598-021-87783-x
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