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Enhanced Osseointegration of Zn-Mg Composites by Tuning the Release of Zn Ions with Sacrificial Mg-Rich Anode Design

  • Hongtao Yang
  • , Xinhua Qu
  • , Wenjiao Lin
  • , Dafu Chen
  • , Donghui Zhu
  • , Kerong Dai*
  • , Yufeng Zheng
  • *此作品的通讯作者
  • Peking University
  • Shanghai Jiao Tong University
  • Lifetech Scientific (Shenzhen) Co. Ltd.
  • Capital Medical University
  • University of North Texas
  • Kumamoto University

科研成果: 期刊稿件文章同行评审

摘要

Relatively slow degradation rate and delayed osseointegration induced by excessive release of Zn 2+ ions are two main disadvantages of the use of pure Zn ion bioabsorbable orthopedic implants. In light of this, we designed a cathodic protection strategy by incorporating Mg, acting as a sacrificial anode, into Zn to form Zn-Mg composites. The performance of novel Zn-Mg composites with regard to degradation behavior and biocompatibility was evaluated systematically under in vitro and in vivo conditions. Macro-galvanic coupling that formed between the Mg-rich phase (anode) and the Zn matrix phase (cathode) accelerated the degradation of Zn-Mg composites as compared to that of pure Zn. Composition analysis revealed ZnO as the dominant product of Zn-Mg composites, followed by calcification matrix formation during the bone healing process. Cytotoxicity assay showed prominently improved cell viability after addition of Mg. Histological analysis manifested delayed osseointegration for the pure Zn group. In contrast, direct contact between new bone and Zn-5Mg composite in multiple locations and increased bone bonding areas were found over time. The synergic biological effect of co-releasing Zn 2+ and Mg 2+ ions by preferential corrosion of sacrificial Mg-rich phase contributed to the ameliorated bone integration. Thus, introducing sacrificial Mg-rich anode is an effective design strategy to increase the degradation rate of pure Zn while simultaneously improving its bone integration ability.

源语言英语
页(从-至)453-467
页数15
期刊ACS Biomaterials Science and Engineering
5
2
DOI
出版状态已出版 - 11 2月 2019
已对外发布

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