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Open-porous magnesium-based scaffolds withstand in vitro corrosion under cyclic loading: A mechanistic study

The successful application of magnesium (Mg) alloys as biodegradable bone substitutes for critical-sized defects may be comprised by their high degradation rate resulting in a loss of mechanical integrity. This study investigates the degradation pattern of an open-porous fluoride-coated Mg-based sca...

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Autores principales: Bonithon, Roxane, Lupton, Colin, Roldo, Marta, Dunlop, Joseph Nicholas, Blunn, Gordon William, Witte, Frank, Tozzi, Gianluca
Formato: Online Artículo Texto
Lenguaje:English
Publicado: KeAi Publishing 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9062748/
https://www.ncbi.nlm.nih.gov/pubmed/35574056
http://dx.doi.org/10.1016/j.bioactmat.2022.04.012
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author Bonithon, Roxane
Lupton, Colin
Roldo, Marta
Dunlop, Joseph Nicholas
Blunn, Gordon William
Witte, Frank
Tozzi, Gianluca
author_facet Bonithon, Roxane
Lupton, Colin
Roldo, Marta
Dunlop, Joseph Nicholas
Blunn, Gordon William
Witte, Frank
Tozzi, Gianluca
author_sort Bonithon, Roxane
collection PubMed
description The successful application of magnesium (Mg) alloys as biodegradable bone substitutes for critical-sized defects may be comprised by their high degradation rate resulting in a loss of mechanical integrity. This study investigates the degradation pattern of an open-porous fluoride-coated Mg-based scaffold immersed in circulating Hanks' Balanced Salt Solution (HBSS) with and without in situ cyclic compression (30 N/1 Hz). The changes in morphological and mechanical properties have been studied by combining in situ high-resolution X-ray computed tomography mechanics and digital volume correlation. Although in situ cyclic compression induced acceleration of the corrosion rate, probably due to local disruption of the coating layer where fatigue microcracks were formed, no critical failures in the overall scaffold were observed, indicating that the mechanical integrity of the Mg scaffolds was preserved. Structural changes, due to the accumulation of corrosion debris between the scaffold fibres, resulted in a significant increase (p < 0.05) in the material volume fraction from 0.52 ± 0.07 to 0.47 ± 0.03 after 14 days of corrosion. However, despite an increase in fibre material loss, the accumulated corrosion products appear to have led to an increase in Young's modulus after 14 days as well as lower third principal strain (εp3) accumulation (−91000 ± 6361 με and −60093 ± 2414 με after 2 and 14 days, respectively). Therefore, this innovative Mg scaffold design and composition provide a bone replacement, capable of sustaining mechanical loads in situ during the postoperative phase allowing new bone formation to be initially supported as the scaffold resorbs.
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spelling pubmed-90627482022-05-13 Open-porous magnesium-based scaffolds withstand in vitro corrosion under cyclic loading: A mechanistic study Bonithon, Roxane Lupton, Colin Roldo, Marta Dunlop, Joseph Nicholas Blunn, Gordon William Witte, Frank Tozzi, Gianluca Bioact Mater Article The successful application of magnesium (Mg) alloys as biodegradable bone substitutes for critical-sized defects may be comprised by their high degradation rate resulting in a loss of mechanical integrity. This study investigates the degradation pattern of an open-porous fluoride-coated Mg-based scaffold immersed in circulating Hanks' Balanced Salt Solution (HBSS) with and without in situ cyclic compression (30 N/1 Hz). The changes in morphological and mechanical properties have been studied by combining in situ high-resolution X-ray computed tomography mechanics and digital volume correlation. Although in situ cyclic compression induced acceleration of the corrosion rate, probably due to local disruption of the coating layer where fatigue microcracks were formed, no critical failures in the overall scaffold were observed, indicating that the mechanical integrity of the Mg scaffolds was preserved. Structural changes, due to the accumulation of corrosion debris between the scaffold fibres, resulted in a significant increase (p < 0.05) in the material volume fraction from 0.52 ± 0.07 to 0.47 ± 0.03 after 14 days of corrosion. However, despite an increase in fibre material loss, the accumulated corrosion products appear to have led to an increase in Young's modulus after 14 days as well as lower third principal strain (εp3) accumulation (−91000 ± 6361 με and −60093 ± 2414 με after 2 and 14 days, respectively). Therefore, this innovative Mg scaffold design and composition provide a bone replacement, capable of sustaining mechanical loads in situ during the postoperative phase allowing new bone formation to be initially supported as the scaffold resorbs. KeAi Publishing 2022-04-29 /pmc/articles/PMC9062748/ /pubmed/35574056 http://dx.doi.org/10.1016/j.bioactmat.2022.04.012 Text en © 2022 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Bonithon, Roxane
Lupton, Colin
Roldo, Marta
Dunlop, Joseph Nicholas
Blunn, Gordon William
Witte, Frank
Tozzi, Gianluca
Open-porous magnesium-based scaffolds withstand in vitro corrosion under cyclic loading: A mechanistic study
title Open-porous magnesium-based scaffolds withstand in vitro corrosion under cyclic loading: A mechanistic study
title_full Open-porous magnesium-based scaffolds withstand in vitro corrosion under cyclic loading: A mechanistic study
title_fullStr Open-porous magnesium-based scaffolds withstand in vitro corrosion under cyclic loading: A mechanistic study
title_full_unstemmed Open-porous magnesium-based scaffolds withstand in vitro corrosion under cyclic loading: A mechanistic study
title_short Open-porous magnesium-based scaffolds withstand in vitro corrosion under cyclic loading: A mechanistic study
title_sort open-porous magnesium-based scaffolds withstand in vitro corrosion under cyclic loading: a mechanistic study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9062748/
https://www.ncbi.nlm.nih.gov/pubmed/35574056
http://dx.doi.org/10.1016/j.bioactmat.2022.04.012
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