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RGDC Peptide-Induced Biomimetic Calcium Phosphate Coating Formed on AZ31 Magnesium Alloy

机译:在AZ31镁合金上形成RGDC肽诱导的仿生磷酸钙涂层

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摘要

Magnesium alloys as biodegradable metal implants have received a lot of interest in biomedical applications. However, magnesium alloys have extremely high corrosion rates a in physiological environment, which have limited their application in the orthopedic field. In this study, calcium phosphate compounds (Ca–P) coating was prepared by arginine–glycine–aspartic acid–cysteine (RGDC) peptide-induced mineralization in 1.5 simulated body fluid (SBF) to improve the corrosion resistance and biocompatibility of the AZ31 magnesium alloys. The adhesion of Ca–P coating to the AZ31 substrates was evaluated by a scratch test. Corrosion resistance and cytocompatibility of the Ca–P coating were investigated. The results showed that the RGDC could effectively promote the nucleation and crystallization of the Ca–P coating and the Ca–P coating had poor adhesion to the AZ31 substrates. The corrosion resistance and biocompatibility of the biomimetic Ca–P coating Mg alloys were greatly improved compared with that of the uncoated sample.
机译:镁合金作为可生物降解的金属植入物已在生物医学应用中引起了广泛兴趣。然而,镁合金在生理环境中具有极高的腐蚀速率,这限制了它们在整形外科领域的应用。在这项研究中,通过精氨酸-甘氨酸-天冬氨酸-半胱氨酸(RGDC)肽诱导的1.5模拟体液(SBF)矿化制备磷酸钙化合物(Ca-P)涂层,以改善AZ31镁的耐腐蚀性和生物相容性合金。通过刮擦测试评估了Ca–P涂层对AZ31基材的附着力。研究了Ca-P涂层的耐腐蚀性和细胞相容性。结果表明,RGDC可以有效地促进Ca-P涂层的形核和结晶,并且Ca-P涂层与AZ31基材的粘合性较差。与未经涂层的样品相比,仿生的Ca-P涂层镁合金的耐腐蚀性和生物相容性得到了极大的提高。

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