4.8 Article

Development of a high-strength Zn-Mn-Mg alloy for ligament reconstruction fixation

期刊

ACTA BIOMATERIALIA
卷 119, 期 -, 页码 485-498

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.actbio.2020.10.032

关键词

Zn alloy; ACL reconstruction; Interference screw; Tendon-bone integration; Peri-tunnel bone loss

资金

  1. National Key R&D Program of China [2016YFC1102500]
  2. National Natural Science Foundation of China [51871020, 81871761, 51771022]
  3. Beijing Natural Science Foundation [7192221, 7172229]
  4. Fundamental Research Funds for the Central Universities [FRF-TP-19-022A3Z]

向作者/读者索取更多资源

A high-strength Zn-0.8Mn-0.4Mg alloy was developed for ligament reconstruction fixation, showing good biocompatibility and promising osteogenic effect. Compared to Ti6Al4V, the Zn alloy screws significantly accelerated new bone formation and promoted tendon-bone integration in ACL reconstruction, contributing to early joint function recovery and rehabilitation training.
Although various biodegradable materials have been investigated for ligament reconstruction fixation in the past decades, only few of them possess a combination of high mechanical properties, appropriate degradation rate, good biocompatibility, and osteogenic effect, thus limiting their clinical applications. A high-strength Zn-0.8Mn-0.4Mg alloy (i.e., Zn08Mn04Mg) with yield strength of 317 MPa was developed to address this issue. The alloy showed good biocompatibility and promising osteogenic effect in vitro . The degradation effects of Zn08Mn04Mg interference screws on the interface between soft tissue and bone were investigated in anterior cruciate ligament (ACL) reconstruction in rabbits. Compared to Ti6Al4V, the Zn alloy screws significantly accelerated the formation of new bone and further induced partial tendon mineralization, which promoted tendon-bone integration. The newly developed screws are believed to facilitate early joint function recovery and rehabilitation training and also avoid screw breakage during insertion, thereby contributing to an extensive clinical prospect. (C) 2020 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.

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