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首页> 外文期刊>RSC Advances >Construction and drug delivery of a fluorescent TPE-bridged cyclodextrin/hyaluronic acid supramolecular assembly
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Construction and drug delivery of a fluorescent TPE-bridged cyclodextrin/hyaluronic acid supramolecular assembly

机译:荧光TPE桥联的环糊精/透明质酸超分子组装体的构建和药物递送

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摘要

A supramolecular assembly was successfully constructed from tetraphenylethylene-bridged b-cyclodextrin tetramers (TPECD) and adamantyl-grafted hyaluronic acids (HAAD) and fully characterized by UV-vis spectroscopy, fluorescence emission spectroscopy, zeta potential, SEM, AFM and TEM. The obtained TPECD-HAAD assembly, which existed as spherical nanoparticles with an average diameter of 50 nm, emitted stronger fluorescence than free TPECD due to the restricted intramolecular rotation. Significantly, this supramolecular assembly can efficiently load the anticancer drug doxorubicin (DOX) into cancer cells, and the resultant DOX@TPECD-HAAD system had higher anticancer ability and fewer side effects than free DOX.
机译:由四苯乙烯桥连的b-环糊精四聚体(TPECD)和金刚烷基接枝的透明质酸(HAAD)成功构建了超分子组装体,并通过紫外可见光谱,荧光发射光谱,ζ电位,SEM,AFM和TEM进行了全面表征。所获得的TPECD-HAAD组件以球形纳米颗粒的形式存在,平均直径为50 nm,由于分子内旋转受到限制,其发射的荧光比游离TPECD的荧光强。值得注意的是,这种超分子组装可以有效地将抗癌药物阿霉素(DOX)加载到癌细胞中,并且所产生的DOX @ TPECD-HAAD系统比游离DOX具有更高的抗癌能力和更少的副作用。

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