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在过氧化氢(HO)和白蛋白存在的情况下,Ti6Al4V的时间依赖性增强腐蚀。

Time-dependent Enhanced Corrosion of Ti6Al4V in the Presence of HO and Albumin.

作者信息

Zhang Yue, Addison Owen, Yu Fei, Troconis Brendy C Rincon, Scully John R, Davenport Alison J

机构信息

School of Metallurgy & Materials, University of Birmingham, Birmingham, B15 2TT, UK.

School of Dentistry, University of Birmingham, Birmingham, B5 7EG, UK.

出版信息

Sci Rep. 2018 Feb 16;8(1):3185. doi: 10.1038/s41598-018-21332-x.

Abstract

There is increasing concern regarding the biological consequences of metal release from implants. However, the mechanisms underpinning implant surface degradation, especially in the absence of wear, are often poorly understood. Here the synergistic effect of albumin and HO on corrosion of Ti6Al4V in physiological saline is studied with electrochemical methods. It is found that albumin induces a time-dependent dissolution of Ti6Al4V in the presence of HO in physiology saline. Potentiostatic polarisation measurements show that albumin supresses dissolution in the presence of HO at short times (<24 h) but over longer time periods (120 h) it significantly accelerates corrosion, which is attributed to albumin-catalysed dissolution of the corrosion product layer resulting in formation of a thinner oxide film. Dissolution of Ti6Al4V in the presence of albumin and HO in physiological saline is also found to be dependent on potential: the titanium ion release rate is found to be higher (0.57 µg/cm) at a lower potential (90 mV), where the oxide capacitance and resistance inferred from Electrochemical Impedance Spectroscopy also suggests a less resistant oxide film. The study highlights the importance of using more realistic solutions, and considering behaviour over longer time periods when testing corrosion resistance of metallic biomaterials.

摘要

人们越来越关注植入物释放金属所带来的生物学后果。然而,对于植入物表面降解的机制,尤其是在无磨损情况下的机制,人们往往了解甚少。在此,我们采用电化学方法研究了白蛋白和过氧化氢(HO)对生理盐水中Ti6Al4V腐蚀的协同作用。研究发现,在生理盐水中存在HO的情况下,白蛋白会诱导Ti6Al4V随时间溶解。恒电位极化测量表明,在短时间内(<24小时),白蛋白在HO存在时会抑制溶解,但在较长时间(120小时)内,它会显著加速腐蚀,这归因于白蛋白催化腐蚀产物层的溶解,导致形成更薄的氧化膜。还发现,在生理盐水中存在白蛋白和HO的情况下,Ti6Al4V的溶解也取决于电位:在较低电位(90mV)下,钛离子释放速率较高(0.57μg/cm),从电化学阻抗谱推断的氧化膜电容和电阻也表明氧化膜的抗性较低。该研究强调了使用更接近实际的溶液以及在测试金属生物材料耐腐蚀性时考虑更长时间行为的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1fe/5816596/2d8b8631f35d/41598_2018_21332_Fig1_HTML.jpg

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