材料科学
羧酸盐
金属有机骨架
金属
多孔性
化学工程
纳米技术
有机化学
冶金
复合材料
吸附
工程类
化学
作者
Sha Lin,Xiangmei Liu,Lei Tan,Zhenduo Cui,Xianjin Yang,Kwk Yeung,Haobo Pan,Shuilin Wu
标识
DOI:10.1021/acsami.7b04810
摘要
Sustained drug release plays a critical role in targeting the therapy of local diseases such as bacterial infections. In the present work, porous iron-carboxylate metal-organic framework [MOF-53(Fe)] nanoparticles (NPs) were designed to entrap the vancomycin (Van) drugs. This system exhibited excellent chemical stability under acidic conditions (pH 7.4, 6.5, and 5.5) and much higher drug-loading capability because of the high porosity and large surface area of MOF NPs. The results showed that the drug-loading ratio of Van could reach 20 wt % and that the antibacterial ratio of the MOF-53(Fe)/Van system against Staphylococcus aureus could reach up to 90%. In addition, this MOF-53(Fe)/Van system exhibited excellent biocompatibility because of its chemical stability and sustained release of iron ions. Hence, these porous MOF NPs are a promising bioplatform not only for local therapy of bacterial infections but also for other biomedical therapies for tissue regeneration.
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