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Construction and drug delivery of a fluorescent TPE-bridged cyclodextrin/hyaluronic acid supramolecular assembly

机译:荧光TPE桥接环糊精/透明质酸超分子组装的构建和药物递送

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A supramolecular assembly was successfully constructed from tetraphenylethylene-bridged β-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:通过四苯基己烯桥β-环糊精四聚体(TPECD)和亚氨基乙基接枝透明质酸(HAAD)成功构建了超分子组件,并用UV-Vis光谱,荧光发射光谱,Zeta电位,SEM,AFM和TEM完全表征。所获得的TPECD-HAAD组件,其作为平均直径为50nm的球形纳米颗粒,由于限制的分子内旋转而比游离TPECD发出更强的荧光。值得注意的是,这种超分子组件可以有效地将抗癌药物Doxorubicin(DOX)载入癌细胞,并且所得DOX @TPECD-HAAD系统具有更高的抗癌能力和比自由DOX更少的副作用。

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