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Physico-chemical and biological evaluation of doxycycline loaded into hybrid oxide-polymer layer on Ti–Mo alloy

机译:Ti-Mo合金中杂化氧化物-聚合物层中强力霉素的理化和生物学评估

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摘要

Oxide-polymer coatings were formed on the surface of the vanadium-free Ti–15Mo titanium alloy. The Ti alloy surface was modified by the plasma electrolytic oxidation process, and then, the polymer layer of a poly (D, -lactide- -glycolide) with doxycycline was formed. The polymer evenly covered the porous oxide layer and filled some of the pores. However, the microstructure of the polymer surface was completely different from that of the PEO layer. The surface morphology, roughness and microstructure of the polymer layer were examined by scanning electron microscopy (SEM) and a confocal microscope. The results confirmed the effectiveness of polymer and doxycycline deposition in their stable chemical forms. The drug analysis was performed by high-performance liquid chromatography. The H NMR technique was used to monitor the course of hydrolytic degradation of PLGA. It was shown that the PLGA layer is hydrolysed within a few weeks, and the polyglycolidyl part of the copolymer is hydrolysed to glycolic acid as first and much faster than the polylactide one to lactic acid. This paper presents influence of different microstructures on the biological properties of modified titanium alloys. Cytocompatibility and bacterial adhesion tests were evaluated using osteoblast-like MG-63 cells and using the reference and strains. The results showed that the optimum concentration of doxycycline was found to inhibit the growth of the bacteria and that the layer is still cytocompatible.
机译:在无钒的Ti-15Mo钛合金的表面上形成了氧化物聚合物涂层。通过等离子电解氧化处理对Ti合金表面进行改性,然后形成具有多西环素的聚(D,-丙交酯-乙交酯)的聚合物层。聚合物均匀地覆盖了多孔氧化物层并填充了一些孔。然而,聚合物表面的微观结构与PEO层的微观结构完全不同。通过扫描电子显微镜(SEM)和共聚焦显微镜检查聚合物层的表面形态,粗糙度和微观结构。结果证实了稳定形式的聚合物和强力霉素的有效性。通过高效液相色谱法进行药物分析。 1 H NMR技术用于监测PLGA的水解降解过程。结果表明,PLGA层在数周内就被水解,并且共聚物的聚糖苷基部分首先被水解为乙醇酸,并且水解速度比聚丙交酯的乳酸快得多。本文介绍了不同的微观结构对改性钛合金生物学性能的影响。使用成骨细胞样MG-63细胞并使用参考菌株和菌株评估细胞相容性和细菌粘附力测试。结果表明,发现最佳浓度的强力霉素可抑制细菌的生长,并且该层仍具有细胞相容性。

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