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Research on an Mg-Zn alloy as a degradable biomaterial.

机译:镁锌合金作为可降解生物材料的研究。

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In this study a binary Mg-Zn magnesium alloy was researched as a degradable biomedical material. An Mg-Zn alloy fabricated with high-purity raw materials and using a clean melting process had very low levels of impurities. After solid solution treatment and hot working the grain size of the Mg-Zn alloy was finer and a uniform single phase was gained. The mechanical properties of this Mg-Zn alloy were suitable for implant applications, i.e. the tensile strength and elongation achieved were approximately 279.5MPa and 18.8%, respectively. The results of in vitro degradation experiments including electrochemical measurements and immersion tests revealed that the zinc could elevate the corrosion potential of Mg in simulated body fluid (SBF) and reduce the degradation rate. The corrosion products on the surface of Mg-Zn were hydroxyapatite (HA) and other Mg/Ca phosphates in SBF. In addition, the influence caused by in vitro degradation on mechanical properties was studied, and the results showed that the bending strength of Mg-Zn alloy dropped sharply in the earlier stage of degradation, while smoothly during the later period. The in vitro cytotoxicity of Mg-Zn was examined. The result 0-1 grade revealed that the Mg-Zn alloy was harmless to L-929 cells. For in vivo experiments, Mg-Zn rods were implanted into the femoral shaft of rabbits. The radiographs illustrated that the magnesium alloy could be gradually absorbed in vivo at about 2.32mm/yr degradation rate obtained by weight loss method. Hematoxylin and eosin (HE) stained section around Mg-Zn rods suggested that there were newly formed bone surrounding the implant. HE stained tissue (containing heart, liver, kidney and spleen tissues) and the biochemical measurements, including serum magnesium, serum creatinine (CREA), blood urea nitrogen (BUN), glutamic-pyruvic transaminase (GPT) and creatine kinase (CK) proved that the in vivo degradation of Mg-Zn did not harm the important organs. Moreover, no adverse effects of hydrogen generated by degradation had been observed and also no negative effects caused by the release of zinc were detected. These results suggested that the novel Mg-Zn binary alloy had good biocompatibility in vivo.
机译:在这项研究中,研究了一种二元Mg-Zn镁合金作为可降解的生物医学材料。使用高纯度原材料制造的Mg-Zn合金,并采用干净的熔化工艺,杂质含量极低。在固溶处理和热加工之后,Mg-Zn合金的晶粒尺寸更细,并且获得了均匀的单相。这种Mg-Zn合金的机械性能适合植入应用,即所达到的拉伸强度和伸长率分别约为279.5MPa和18.8%。体外降解实验(包括电化学测量和浸没测试)的结果表明,锌可以提高模拟体液(SBF)中Mg的腐蚀电位并降低降解速率。在SBF中,Mg-Zn表面的腐蚀产物是羟基磷灰石(HA)和其他Mg / Ca磷酸盐。此外,研究了体外降解对机械性能的影响,结果表明,Mg-Zn合金的抗弯强度在降解的早期急剧下降,而在后期则平稳。检查了Mg-Zn的体外细胞毒性。 0-1级结果表明Mg-Zn合金对L-929细胞无害。为了进行体内实验,将Mg-Zn棒植入兔子的股骨干中。放射线照片表明,镁合金可以通过失重法以约2.32mm / yr的降解速率在体内逐渐吸收。 Mg-Zn棒周围的苏木精和曙红(HE)染色切片表明植入物周围有新形成的骨头。 HE染色的组织(包含心脏,肝脏,肾脏和脾脏组织)和生化指标,包括血清镁,血清肌酐(CREA),血尿素氮(BUN),谷氨酸-丙酮酸转氨酶(GPT)和肌酸激酶(CK)已证明Mg-Zn在体内的降解不会损害重要器官。此外,未观察到由降解产生的氢的不利影响,也未检测到由锌的释放引起的不利影响。这些结果表明,新型Mg-Zn二元合金在体内具有良好的生物相容性。

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