National and Local Joint Engineering Research Center of Biomedical Functional Materials, School of Chemistry and Materials Science, Nanjing Normal University , Nanjing 210046, China.
ACS Appl Mater Interfaces. 2017 Jun 7;9(22):18609-18618. doi: 10.1021/acsami.7b05163. Epub 2017 May 25.
Mesoporous silica has been developed for the modification of titanium surfaces that are used as implant materials. Yet, the traditional modification methods failed to effectively construct mesoporous silica on the titanium surface evenly and firmly, in which the interaction between mesoporous silica and titanium was mainly physical. Here, in situ growth of mesoporous silica on a titanium surface was performed using a simple evaporation-induced self-assembly strategy. Meantime, in situ introduction of drugs (heparin and vancomycin) to mesoporous silica was also adopted to improve the drug-loading amount. Both the above-mentioned processes were completed at the same time. Transmission electron microscopy, N adsorption-desorption isotherms, Fourier transform infrared spectroscopy, scanning electron microscopy, and water contact angle measurements were used to characterize the structure of the mesoporous silica film. Results indicated that the mesoporous silica film that in situ grew on the titanium surface was smooth, thin, transparent, and stable. Cytotoxicity, proliferation performance of osteoblast cells, and in vitro and in vivo studies of the antibacterial activity of the coating were tested. This is the first study to modify the titanium surface by the in situ growth of a mesoporous silica coating with two kinds of drugs. The stability of the mesoporous silica coating can be attributed to the chemical bonding between dopamine and silicon hydroxyl of the mesoporous silica coating, and the smooth surface of mesoporous silica is a result of the method of in situ growth. The large amount of drug-loading also could be ascribed to the in situ introduction of drugs during the synthetic process. The strategy proposed in this work will bring more possibilities for the preparation of advanced functional materials based on the combination of mesoporous structure and metallic materials.
介孔硅已被开发用于修饰钛表面,钛表面被用作植入材料。然而,传统的修饰方法未能有效地将介孔硅均匀且牢固地构建在钛表面上,其中介孔硅与钛之间的相互作用主要是物理的。在这里,使用简单的蒸发诱导自组装策略在钛表面上原位生长介孔硅。同时,还采用原位引入药物(肝素和万古霉素)来介孔硅来提高载药量。上述两个过程同时完成。通过透射电子显微镜、N2 吸附-解吸等温线、傅里叶变换红外光谱、扫描电子显微镜和水接触角测量来表征介孔硅膜的结构。结果表明,原位生长在钛表面上的介孔硅膜光滑、薄、透明且稳定。对涂层的细胞毒性、成骨细胞增殖性能以及体外和体内抗菌活性进行了研究。这是首次通过原位生长具有两种药物的介孔硅涂层来修饰钛表面的研究。介孔硅涂层的稳定性归因于多巴胺与介孔硅涂层硅羟基之间的化学键,介孔硅的光滑表面是原位生长方法的结果。大量的载药量也归因于在合成过程中引入了原位药物。本工作中提出的策略将为基于介孔结构和金属材料的组合制备先进功能材料带来更多可能性。