Feng Wenchao, Geng Zhen, Li Zhaoyang, Cui Zhenduo, Zhu Shengli, Liang Yanqin, Liu Yunde, Wang Renfeng, Yang Xianjin
School of Materials Science and Engineering, Tianjin University, Tianjin 300072, China.
School of Materials Science and Engineering, Tianjin University, Tianjin 300072, China; Tianjin Key Laboratory of Composite and Functional Materials, Tianjin 300072, China.
Mater Sci Eng C Mater Biol Appl. 2016 May;62:105-12. doi: 10.1016/j.msec.2016.01.046. Epub 2016 Jan 21.
Bacterial infections have been identified as the main cause of orthopaedic implant failure. Owing to their high antibiotic delivery efficiency, titania nanotubes loaded with antibiotics constitute one of the most promising strategies for suppressing bacterial infections. However, it is difficult to control the drug-release behaviour of such nanotubes. Although sealing the nanotubes with a polymer solution provides sustained release effects to a certain extent, it inevitably influences their initial antibacterial activity. This study reports on the controlled release of gentamicin sulphate (GS) from titania nanotube surfaces whereby their initial antibacterial activity remains unaffected. Titania nanotubes were fabricated via electrochemical anodization and loaded with GS through physical adsorption. Experimental results showed that this loading method is feasible and efficient. The GS-loaded titania nanotubes were further covered by a thin film comprising a mixture of GS and chitosan (GSCH). The release kinetics confirmed that the drug release could be controlled by this thin film. Moreover, such a film was shown to not only inhibit initial bacterial adherence owing to its strong antibacterial properties but also enhance cell viability. Thus, GS-loaded titania nanotubes coated with GSCH have considerable potential as biomaterials for preventing initial release and peri-implant infection in the field of orthopaedics.
细菌感染已被确认为骨科植入物失败的主要原因。由于其高抗生素递送效率,负载抗生素的二氧化钛纳米管构成了抑制细菌感染最有前景的策略之一。然而,难以控制此类纳米管的药物释放行为。虽然用聚合物溶液密封纳米管在一定程度上提供了缓释效果,但不可避免地会影响其初始抗菌活性。本研究报道了硫酸庆大霉素(GS)从二氧化钛纳米管表面的可控释放,在此过程中其初始抗菌活性不受影响。通过电化学阳极氧化制备二氧化钛纳米管,并通过物理吸附负载GS。实验结果表明这种负载方法是可行且有效的。负载GS的二氧化钛纳米管进一步被包含GS和壳聚糖混合物(GSCH)的薄膜覆盖。释放动力学证实药物释放可由此薄膜控制。此外,这种薄膜不仅因其强大的抗菌性能抑制初始细菌黏附,还能提高细胞活力。因此,涂覆有GSCH的负载GS的二氧化钛纳米管作为骨科领域预防初始释放和植入物周围感染的生物材料具有相当大的潜力。