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将肝素/比伐卢定原位掺入可生物降解镁的植酸涂层中,具有改善的防腐和生物相容性。

In situ incorporation of heparin/bivalirudin into a phytic acid coating on biodegradable magnesium with improved anticorrosion and biocompatible properties.

作者信息

Chen Yingqi, Zhang Xuan, Zhao Sheng, Maitz Manfred F, Zhang Wentai, Yang Su, Mao Jinlong, Huang Nan, Wan Guojiang

机构信息

Key Laboratory of Advanced Technologies of Materials, Ministry of Education, College of Materials Science and Engineering, Southwest Jiaotong University, Chengdu, 610031, China.

出版信息

J Mater Chem B. 2017 Jun 14;5(22):4162-4176. doi: 10.1039/c6tb03157a. Epub 2017 May 17.

DOI:10.1039/c6tb03157a
PMID:32264147
Abstract

Heparin (Hep) or bivalirudin (BVLD) were immobilized in an organic phytic acid (PA) coating on Mg by an in situ chemical route. Such a drug-loaded PA coating was designed to enhance both corrosion control and biocompatibility. It was found that both Hep- and BVLD-loaded PA coatings exhibited a dual role in effectively controlling corrosion as well as providing a biofunctional effect. Experiments involving electrochemical corrosion and in vitro degradation by immersion revealed that PA&Hep- and PA&BVLD-coated Mg had the same effect or even slower corrosion/degradation in phosphate buffered saline compared to PA-coated Mg, and it degraded significantly slower than untreated Mg. Moreover, Hep- or BVLD-loaded PA coatings showed relatively good hemocompatibility, with a prolonged clotting time, inhibited platelets adhesion as well as reduced hemolysis compared to untreated Mg. In addition, both PA&Hep and PA&BVLD coatings promoted endothelial cells growth and restrained the proliferation of smooth muscle cells. In vivo assays indicated that PA&Hep-coated Mg exhibited a significant difference in mass loss compared to untreated Mg, as well as better histocompatibility than other samples. These results demonstrate that our coating strategy shows a great potential in surface modification of biodegradable Mg. Finally, the mechanism for the incorporation of the drugs into the PA coating is discussed from both theoretical and practical perspectives.

摘要

通过原位化学途径将肝素(Hep)或比伐卢定(BVLD)固定在镁表面的有机植酸(PA)涂层中。这种载药PA涂层旨在增强腐蚀控制和生物相容性。研究发现,负载肝素和比伐卢定的PA涂层在有效控制腐蚀以及提供生物功能效应方面均发挥双重作用。涉及电化学腐蚀和浸泡体外降解的实验表明,与PA涂层镁相比,PA&Hep涂层和PA&BVLD涂层的镁在磷酸盐缓冲盐水中具有相同的效果,甚至腐蚀/降解速度更慢,且其降解速度明显慢于未处理的镁。此外,负载肝素或比伐卢定的PA涂层显示出相对良好的血液相容性,与未处理的镁相比,凝血时间延长,血小板粘附受到抑制,溶血减少。另外,PA&Hep涂层和PA&BVLD涂层均促进内皮细胞生长并抑制平滑肌细胞增殖。体内试验表明,与未处理的镁相比,PA&Hep涂层的镁在质量损失方面存在显著差异,并且组织相容性优于其他样品。这些结果表明,我们的涂层策略在可生物降解镁的表面改性方面具有巨大潜力。最后,从理论和实际角度讨论了药物掺入PA涂层的机制。

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