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Degradation behavior of ZE21C magnesium alloy suture anchors and their effect on ligament-bone junction repair
Current materials comprising suture anchors used to reconstruct ligament-bone junctions still have limitation in biocompatibility, degradability or mechanical properties. Magnesium alloys are potential bone implant materials, and Mg(2+) has been shown to promote ligament-bone healing. Here, we used...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
KeAi Publishing
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9986500/ https://www.ncbi.nlm.nih.gov/pubmed/36891259 http://dx.doi.org/10.1016/j.bioactmat.2023.02.021 |
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author | Ma, Delin Wang, Jun Zheng, Mingran Zhang, Yuan Huang, Junfei Li, Wenxiang Ding, Yiwen Zhang, Yunhao Zhu, Shijie Wang, Liguo Wu, Xiaochao Guan, Shaokang |
author_facet | Ma, Delin Wang, Jun Zheng, Mingran Zhang, Yuan Huang, Junfei Li, Wenxiang Ding, Yiwen Zhang, Yunhao Zhu, Shijie Wang, Liguo Wu, Xiaochao Guan, Shaokang |
author_sort | Ma, Delin |
collection | PubMed |
description | Current materials comprising suture anchors used to reconstruct ligament-bone junctions still have limitation in biocompatibility, degradability or mechanical properties. Magnesium alloys are potential bone implant materials, and Mg(2+) has been shown to promote ligament-bone healing. Here, we used Mg-2 wt.% Zn-0.5 wt.% Y-1 wt.% Nd-0.5 wt.% Zr (ZE21C) alloy and Ti6Al4V (TC4) alloy to prepare suture anchors to reconstruct the patellar ligament-tibia in SD rats. We studied the degradation behavior of the ZE21C suture anchor via in vitro and in vivo experiments and assessed its reparative effect on the ligament-bone junction. In vitro, the ZE21C suture anchor degraded gradually, and calcium and phosphorus products accumulated on its surface during degradation. In vivo, the ZE21C suture anchor could maintain its mechanical integrity within 12 weeks of implantation in rats. The tail of the ZE21C suture anchor in high stress concentration degraded rapidly during the early implantation stage (0–4weeks), while bone healing accelerated the degradation of the anchor head in the late implantation stage (4–12weeks). Radiological, histological, and biomechanical assays indicated that the ZE21C suture anchor promoted bone healing above the suture anchor and fibrocartilaginous interface regeneration in the ligament-bone junction, leading to better biomechanical strength than the TC4 group. Hence, this study provides a basis for further research on the clinical application of degradable magnesium alloy suture anchors. |
format | Online Article Text |
id | pubmed-9986500 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | KeAi Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-99865002023-03-07 Degradation behavior of ZE21C magnesium alloy suture anchors and their effect on ligament-bone junction repair Ma, Delin Wang, Jun Zheng, Mingran Zhang, Yuan Huang, Junfei Li, Wenxiang Ding, Yiwen Zhang, Yunhao Zhu, Shijie Wang, Liguo Wu, Xiaochao Guan, Shaokang Bioact Mater Article Current materials comprising suture anchors used to reconstruct ligament-bone junctions still have limitation in biocompatibility, degradability or mechanical properties. Magnesium alloys are potential bone implant materials, and Mg(2+) has been shown to promote ligament-bone healing. Here, we used Mg-2 wt.% Zn-0.5 wt.% Y-1 wt.% Nd-0.5 wt.% Zr (ZE21C) alloy and Ti6Al4V (TC4) alloy to prepare suture anchors to reconstruct the patellar ligament-tibia in SD rats. We studied the degradation behavior of the ZE21C suture anchor via in vitro and in vivo experiments and assessed its reparative effect on the ligament-bone junction. In vitro, the ZE21C suture anchor degraded gradually, and calcium and phosphorus products accumulated on its surface during degradation. In vivo, the ZE21C suture anchor could maintain its mechanical integrity within 12 weeks of implantation in rats. The tail of the ZE21C suture anchor in high stress concentration degraded rapidly during the early implantation stage (0–4weeks), while bone healing accelerated the degradation of the anchor head in the late implantation stage (4–12weeks). Radiological, histological, and biomechanical assays indicated that the ZE21C suture anchor promoted bone healing above the suture anchor and fibrocartilaginous interface regeneration in the ligament-bone junction, leading to better biomechanical strength than the TC4 group. Hence, this study provides a basis for further research on the clinical application of degradable magnesium alloy suture anchors. KeAi Publishing 2023-02-27 /pmc/articles/PMC9986500/ /pubmed/36891259 http://dx.doi.org/10.1016/j.bioactmat.2023.02.021 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Ma, Delin Wang, Jun Zheng, Mingran Zhang, Yuan Huang, Junfei Li, Wenxiang Ding, Yiwen Zhang, Yunhao Zhu, Shijie Wang, Liguo Wu, Xiaochao Guan, Shaokang Degradation behavior of ZE21C magnesium alloy suture anchors and their effect on ligament-bone junction repair |
title | Degradation behavior of ZE21C magnesium alloy suture anchors and their effect on ligament-bone junction repair |
title_full | Degradation behavior of ZE21C magnesium alloy suture anchors and their effect on ligament-bone junction repair |
title_fullStr | Degradation behavior of ZE21C magnesium alloy suture anchors and their effect on ligament-bone junction repair |
title_full_unstemmed | Degradation behavior of ZE21C magnesium alloy suture anchors and their effect on ligament-bone junction repair |
title_short | Degradation behavior of ZE21C magnesium alloy suture anchors and their effect on ligament-bone junction repair |
title_sort | degradation behavior of ze21c magnesium alloy suture anchors and their effect on ligament-bone junction repair |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9986500/ https://www.ncbi.nlm.nih.gov/pubmed/36891259 http://dx.doi.org/10.1016/j.bioactmat.2023.02.021 |
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