In vitro corrosion behavior and in vivo biodegradation of biomedical β-Ca3(PO4)2/Mg-Zn composites

被引:65
作者
Yu, Kun [2 ,3 ]
Chen, Liangjian [1 ,3 ]
Zhao, Jun [2 ]
Li, Shaojun [2 ]
Dai, Yilong [2 ]
Huang, Qiao [2 ]
Yu, Zhiming [2 ]
机构
[1] Cent S Univ, XiangYa Hosp 3, Changsha 410083, Hunan, Peoples R China
[2] Cent S Univ, Sch Mat Sci & Engn, Changsha 410083, Hunan, Peoples R China
[3] State Key Lab Powder Met, Changsha 410083, Hunan, Peoples R China
关键词
Composite; Corrosion product; Simulated body fluid; Mechanical properties; Cytotoxicity; MAGNESIUM ALLOYS;
D O I
10.1016/j.actbio.2012.04.009
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
In this study 5, 10 and 15% beta-Ca-3(PO4)(2)/Mg-Zn composites were prepared through powder metallurgy methods, and their corrosion behavior and mechanical properties were studied in simulated body fluid (SBF) at 37 degrees C. The 10% beta-Ca-3(PO4)(2)/Mg-Zn composite was selected for cytocompatibility assessment and in vivo biodegradation testing. The results identified the alpha-Mg, MgZn and beta-Ca-3(PO4)(2) phases in these sintered composites. The density and elastic modulus of the beta-Ca-3(PO4)(2)/Mg-6% Zn composite match those of natural bone, and the strength is approximately double that of natural bone. The 10% beta-Ca-3(PO4)(2)/Mg-6% Zn composites exhibit good corrosion resistance, as determined by a 30 day immersion test and electrochemical measurements in SBF at 37 degrees C. The 10% beta-Ca-3(PO4)(2)/Mg-6% Zn composite is safe for cellular applications, with a cytotoxicity grade of similar to 0-1 against L929 cells in in vitro testing. The beta-Ca-3(PO4)(2)/Mg-6% Zn composite also exhibits good biocompatibility with the tissue and the important visceral organs the heart, kidney and liver of experimental rabbits. The composite has a suitable degradation rate and improves the concrescence of a pre-broken bone. The corrosion products, such as Mg(OH)(2) and Ca-5(PO4)(6)(OH)(2), can improve the biocompatibility of the beta-Ca-3(PO4)(2)/Mg-Zn composite. (C) 2012 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:2845 / 2855
页数:11
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