纳米载体
谷胱甘肽
纳米团簇
荧光
药物输送
纳米颗粒
化学
核化学
纳米技术
材料科学
有机化学
物理
量子力学
酶
作者
Qiu Li,Yanbao Zhao,Na Cao,Liuqin Cao,Lei Sun,Xueyan Zou
标识
DOI:10.1016/j.snb.2016.04.136
摘要
To reduce the premature release of encapsulated drug, glutathione-responsive fluorescent porous silica (pSiO2) nanocarriers were developed by encapsulating Ag nanoclusters (Ag NCs) and capped with Ag nanoparticles (Ag NPs). Ag NCs/porous silica (Ag NCs/pSiO2) nanospheres (NSs) have an average diameter of 45 nm and large specific surface with Brunauer-Emmett-Teller (BET) area of 453 m2 g−1. After loading N-(2-Mercaptopropionyl) glycine (MPG), the absorbed Ag+ ions were in situ reduced to Ag NPs and capped on the outer surfaces of Ag NCs/pSiO2 NSs as gatekeepers to regulate the release of drugs. In the absence of glutathione (GSH), the release rate is below 8% within 12 h; while in the presence of 2 mM GSH, the amount released reaches 70% within 8 h. The Ag NPs-gated Ag NCs/pSiO2 NSs displayed excellent GSH-responsive release. The incorporated Ag NCs presented novel drug-dependent fluorescence, which could be used to trace the drug release. In addition, the Ag NPs-gated Ag NCs/pSiO2 NSs displayed excellent antibacterial activity against both Gram-positive and Gram-negative bacteria.
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