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介孔硅纳米粒子上的 pH 和谷胱甘肽双重响应动态交联超分子网络用于控制抗癌药物释放。

pH and Glutathione Dual-Responsive Dynamic Cross-Linked Supramolecular Network on Mesoporous Silica Nanoparticles for Controlled Anticancer Drug Release.

机构信息

School of Chemistry and Chemical Engineering, Tianjin Key Laboratory of Organic Solar Cells and Photochemical Conversion, School of Material Science and Engineering, Tianjin University of Technology , Tianjin 300384, People's Republic of China.

出版信息

ACS Appl Mater Interfaces. 2015 Dec 30;7(51):28656-64. doi: 10.1021/acsami.5b10534. Epub 2015 Dec 15.

Abstract

A dynamic cross-linked supramolecular network of poly(glycidyl methacrylate)s derivative chains was constructed on mesoporous silica nanoparticles via disulfide bond and ion-dipole interactions between cucurbit[7]urils and protonated diamines in the polymer chains. This kind of multifunctional organic-inorganic hybrid material with pH- and glutathione- (GSH-) stimuli responsiveness can be applied to anticancer drug delivery and controlled release. Good release performance toward doxorubicin hydrochloride (DOX) was achieved under the simulative tumor intracellular environment (pH = 5.0, CGSH = 2-10 mM). Significantly, the release amount of DOX increased upon lowering the solution pH value and increasing the concentration of GSH, as demonstrated by a series of controlled release experiments. Furthermore, the DOX-loaded hybrid nanomaterials displayed apparent cell-growth inhibition effects to cancer cell lines, as evidenced by MTT assay and confocal laser scanning microscopy.

摘要

通过介孔硅纳米粒子上聚(甲基丙烯酸缩水甘油酯)衍生物链之间的二硫键和葫芦[7]脲与聚合物链中质子化二胺之间的离子-偶极相互作用,构建了一种动态交联的超分子网络。这种具有 pH 和谷胱甘肽(GSH)刺激响应的多功能有机-无机杂化材料可应用于抗癌药物的传递和控制释放。在模拟肿瘤细胞内环境(pH = 5.0,CGSH = 2-10 mM)下,对盐酸阿霉素(DOX)表现出良好的释放性能。通过一系列的控制释放实验,显著地,当降低溶液 pH 值和增加 GSH 浓度时,DOX 的释放量增加。此外,负载 DOX 的杂化纳米材料对癌细胞系表现出明显的细胞生长抑制作用,这一点通过 MTT 测定和共聚焦激光扫描显微镜得到了证明。

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