Zhang Zhao-Qi, Wang Li, Zeng Mei-Qi, Zeng Rong-Chang, Kannan M Bobby, Lin Cun-Guo, Zheng Yu-Feng
Corrosion Laboratory for Light Metals, College of Material Science and Engineering, Shandong University of Science and Technology, Qingdao, 266590, China.
State Key Laboratory for Marine Corrosion and Protection, Luoyang Ship Material Research Institute, Qingdao, 266101, China.
Bioact Mater. 2020 Mar 30;5(2):398-409. doi: 10.1016/j.bioactmat.2020.03.005. eCollection 2020 Jun.
Protein exerts a critical influence on the degradation behavior of absorbable magnesium (Mg)-based implants. However, the interaction mechanism between protein and a micro-arc oxidation (MAO) coating on Mg alloys remains unclear. Hereby, a MAO coating was fabricated on AZ31 Mg alloy. And its degradation behavior in phosphate buffer saline (PBS) containing bovine serum albumin (BSA) was investigated and compared with that of the uncoated alloy. Surface morphologies and chemical compositions were studied using Field-emission scanning electron microscope (FE-SEM), Fourier transform infrared spectrophotometer (FT-IR) and X-ray diffraction (XRD). The degradation behavior of the bare Mg alloy and its MAO coating was studied through electrochemical and hydrogen evolution tests. Cytotoxicity assay was applied to evaluate the biocompatibility of Mg alloy substrate and MAO coating. Results indicated that the presence of BSA decreased the degradation rate of Mg alloy substrate because BSA (RCH(NH)COO‾) molecules combined with Mg ions to form (RCH(NH)COO)Mg and thus inhibited the dissolution of Mg(OH) by impeding the attack of Cl‾ ions. In the case of MAO coated Mg alloy, the adsorption of BSA on MAO coating and the formation of (RCH(NH)COO)Mg exhibited a synergistic effect and enhanced the corrosion resistance of the coated alloy significantly. Furthermore, cell bioactive assay suggested that the MAO coating had good viability for MG63 cells due to its high surface area.
蛋白质对可吸收镁基植入物的降解行为具有关键影响。然而,蛋白质与镁合金上微弧氧化(MAO)涂层之间的相互作用机制仍不清楚。在此,在AZ31镁合金上制备了MAO涂层。研究了其在含牛血清白蛋白(BSA)的磷酸盐缓冲盐水(PBS)中的降解行为,并与未涂层合金的降解行为进行了比较。使用场发射扫描电子显微镜(FE-SEM)、傅里叶变换红外光谱仪(FT-IR)和X射线衍射(XRD)研究了表面形貌和化学成分。通过电化学和析氢试验研究了裸镁合金及其MAO涂层的降解行为。应用细胞毒性试验评估镁合金基体和MAO涂层的生物相容性。结果表明,BSA的存在降低了镁合金基体的降解速率,因为BSA(RCH(NH)COO‾)分子与镁离子结合形成(RCH(NH)COO)Mg,从而通过阻止Cl‾离子的侵蚀抑制了Mg(OH)的溶解。对于MAO涂层镁合金,BSA在MAO涂层上的吸附以及(RCH(NH)COO)Mg的形成表现出协同效应,显著提高了涂层合金的耐腐蚀性。此外,细胞生物活性试验表明,MAO涂层由于其高表面积对MG63细胞具有良好的活力。