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Localized Controlled Drug Delivery from Mesoporous Implants

机译:来自中孔植入物的局部受控药物递送

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Mesoporous materials possess both a well-defined topography on the nanometer scale, and they may serve as hosts for drugs. In this work, titanium implants coated with mesoporous TiO_2 thin films have been evaluated both in vitro and in vivo. Material characterization showed that, long-range ordered mesoporous TiO_2, with a pore-size of 6 nm, and a narrow pore-size distribution were obtained. An in vivo study demonstrated that the films were robust enough to withstand the implantation procedure. The in vitro apatite formation experiments showed that formation of apatite was higher on the mesoporous surface compared to its nonporous counterpart. In a separate in vivo study, two osteoporosis drugs, alendronate (ALN) and raloxifene (RLX), were immobilised into the nanoporous oxide films. The in vitro drug release tests carried out showed a sustained release of both drugs. The osteogenic response after 28 days of implantation of the drug-loaded implants showed a significantly improved bone fixation.
机译:中孔材料具有纳米尺度的明确鉴定的地形,它们可以作为药物的主体。在这项工作中,已经在体外和体内评估涂有介孔TiO_2薄膜的钛植入物。材料表征显示,获得了孔径为6nm的远程有序的介孔TiO_2和窄孔尺寸分布。体内研究表明,薄膜足够坚固以承受植入程序。体外磷灰石形成实验表明,与其无孔对应物相比,在中孔表面上形成磷灰石的形成。在体内研究中,将两个骨质疏松症药物,醛酸盐(AlN)和雷洛昔芬(RLX)固定在纳米多孔氧化物膜中。进行的体外药物释放试验表明两种药物的持续释放。植入药物植入物28天后的骨质发生反应显示出显着改善的骨固定。

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