Silver nanoparticle-gated fluorescence porous silica nanospheres for glutathione-responsive drug delivery

被引:28
|
作者
Qiu, Li [1 ]
Zhao, Yanbao [1 ]
Cao, Na [1 ]
Cao, Liuqin [1 ]
Sun, Lei [1 ]
Zou, Xueyan [1 ]
机构
[1] Henan Univ, Engn Res Ctr Nanomat, Kaifeng 475004, Peoples R China
来源
SENSORS AND ACTUATORS B-CHEMICAL | 2016年 / 234卷
基金
中国国家自然科学基金;
关键词
Porous silica; Glutathione-responsive; Drug delivery; MESOPOROUS SILICA; RELEASE; NANOCLUSTERS;
D O I
10.1016/j.snb.2016.04.136
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
To reduce the premature release of encapsulated drug, glutathione-responsive fluorescent porous silica (pSiO(2)) nanocarriers were developed by encapsulating Ag nanoclusters (Ag NCs) and capped with Ag nanoparticles (Ag NPs). Ag NCs/porous silica (Ag NCs/pSiO(2)) nanospheres (NSs) have an average diameter of 45 nm and large specific surface with Brunauer-Emmett-Teller (BET) area of 453 m(2) 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/pSiO(2) 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/pSiO(2) 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/pSiO(2) NSs displayed excellent antibacterial activity against both Gram-positive and Gram-negative bacteria. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:21 / 26
页数:6
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