功能化二硫化钼纳米载药复合物的制备及体外药物释放研究

章学易, 吴建荣, 钱倩倩, 牛世伟, 朱利民*

化工新型材料 ›› 2019, Vol. 47 ›› Issue (5) : 269 -272.

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化工新型材料 ›› 2019, Vol. 47 ›› Issue (5) : 269-272.
开发与应用

功能化二硫化钼纳米载药复合物的制备及体外药物释放研究

    章学易, 吴建荣, 钱倩倩, 牛世伟, 朱利民*
作者信息 +

Study on the preparation and in vitro drug release of functionalized MoS2 nanocomposite

  • Zhang Xueyi, Wu Jianrong, Qian Qianqian, Niu Shiwei, Zhu Limin
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摘要

采用二硫化钼(MoS2)表面接枝硫辛酸(LA)修饰的聚乙二醇(PEG)(LA-PEG),以增加其生物相容性,进一步接枝聚乙烯亚胺(PEI),用以连接牛血清蛋白(BSA)修饰的叶酸(FA),构建主动靶向体系叶酸-牛血清蛋白-聚乙烯亚胺-硫辛酸-二硫化钼-硫辛酸-聚乙二醇(FA-BSA-PEI-LA-MoS2-LA-PEG),并对产物的形貌及理化性质进行测试。研究结果表明,制得的产物的水动力学直径约133nm,适合用作抗癌药物载体,以阿霉素(DOX)为模型药物,研究产物的载药能力和体外药物释放行为,在pH=5.0,近红外光照射条件下,经过68h,产物负载的DOX的累计释放量为67.8%,具有良好的载药能力和应用价值。

Abstract

Lipophilic (LA) modified polyethylene glycol (PEG)(LA-PEG) was grafted to the surface of molybdenum disulfide (MoS2) to improve its biocompatibility,and further modified by graft polyethylenimine (PEI) which was used to link bovine serum albumin (BSA) modified folic acid (FA).Thus the drug delivery system FA-BSA-PEI-LA-MoS2-LA-PEG was constructed.The morphology and physicochemical properties of materials were characterized.The hydrodynamic size of materials was 133nm,which was suitable for using as a carrier of anticancer drugs.The drug loading efficiency and in vitro drug release behavior of complexes were investigated with DOX as model drug.The results showed that the cumulative drug release was 67.8% after 68h with NIR at pH 5.0.The drug delivery system had good drug-loading ability as well as application value.

关键词

二硫化钼 / 近红外光刺激响应 / pH敏感 / 药物控释 / 乳腺癌靶向

Key words

molybdenum disulfide / near-infrared light stimulus response / pH stimulus response / drug controlled release / breast cancer targeting

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功能化二硫化钼纳米载药复合物的制备及体外药物释放研究[J]. 化工新型材料, 2019, 47(5): 269-272 DOI:

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基金资助

上海市科学技术委员会资助项目(16410723700);生物医用纺织材料“111工程”中国教育部(B07024)

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