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Fabrication of functional hollow microspheres constructed from MOF shells: Promising drug delivery systems with high loading capacity and targeted transport

机译:由MOF壳构成的功能性空心微球的制造:具有高负载能力和针对性运输的有前途的药物输送系统

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摘要

An advanced multifunctional, hollow metal-organic framework (MOF) drug delivery system with a high drug loading level and targeted delivery was designed and fabricated for the first time and applied to inhibit tumour cell growth. This hollow MOF targeting drug delivery system was prepared via a simple post-synthetic surface modification procedure, starting from hollow ZIF-8 successfully obtained for the first time via a mild phase transformation under solvothermal conditions. As a result, the hollow ZIF-8 exhibits a higher loading capacity for the model anticancer drug 5-fluorouracil (5-FU). Subsequently, 5-FU-loaded ZIF-8 was encapsulated into polymer layers (FA-CHI-5-FAM) with three components: a chitosan (CHI) backbone, the imaging agent 5-carboxyfluorescein (5-FAM), and the targeting reagent folic acid (FA). Thus, an advanced drug delivery system, ZIF-8/5-FU@FA-CHI-5-FAM, was fabricated. A cell imaging assay demonstrated that ZIF-8/5-FU@FA-CHI-5-FAM could target and be taken up by MGC-803 cells. Furthermore, the as-prepared ZIF-8/5-FU@FA-CHI-5-FAM exhibited stronger cell growth inhibitory effects on MGC-803 cells because of the release of 5-FU, as confirmed by a cell viability assay. In addition, a drug release experiment in vitro indicated that ZIF-8/5-FU@FA-CHI-5-FAM exhibited high loading capacity (51%) and a sustained drug release behaviour. Therefore, ZIF-8/5-FU@FA-CHI-5-FAM could provide targeted drug transportation, imaging tracking and localized sustained release.
机译:具有高载药量和靶向递送功能的先进多功能,中空金属有机骨架(MOF)药物递送系统是首次设计和制造,并用于抑制肿瘤细胞的生长。这种中空的MOF靶向药物递送系统是通过简单的合成后表面修饰程序制备的,该过程是通过在溶剂热条件下通过温和相变首次成功获得的中空ZIF-8开始的。结果,中空的ZIF-8对模型抗癌药5-氟尿嘧啶(5-FU)表现出更高的负载能力。随后,将加载有5-FU的ZIF-8封装到具有以下三个成分的聚合物层(FA-CHI-5-FAM)中:壳聚糖(CHI)主链,显像剂5-羧基荧光素(5-FAM)和靶向叶酸试剂(FA)。因此,制造了先进的药物输送系统ZIF-8 / 5-FU @ FA-CHI-5-FAM。细胞成像分析表明ZIF-8 / 5-FU @ FA-CHI-5-FAM可以靶向并被MGC-803细胞吸收。此外,如所制备的ZIF-8 / 5-FU @ FA-CHI-5-FAM由于5-FU的释放而对MGC-803细胞表现出更强的细胞生长抑制作用,如细胞活力测定所证实的。此外,体外药物释放实验表明ZIF-8 / 5-FU @ FA-CHI-5-FAM具有高载药量(51%)和持续的药物释放行为。因此,ZIF-8 / 5-FU @ FA-CHI-5-FAM可以提供有针对性的药物运输,成像跟踪和局部持续释放。

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