Intracellular Proteolytic Disassembly of Self-Quenched Near-Infrared Nanoparticles Turning Fluorescence on for Tumor-Targeted Imaging

被引:24
|
作者
Jiang, Jinhui [1 ]
Zhao, Zhibin [2 ,3 ]
Hai, Zijuan [1 ]
Wang, Hongyong [4 ]
Liang, Gaolin [1 ]
机构
[1] Univ Sci & Technol China, Dept Chem, CAS Key Lab Soft Matter Chem, 96 Jinzhai Rd, Hefei 230026, Anhui, Peoples R China
[2] Univ Sci & Technol China, Liver Immunol Lab, Inst Immunol, Hefei 230027, Anhui, Peoples R China
[3] Univ Sci & Technol China, Sch Life Sci, Hefei 230027, Anhui, Peoples R China
[4] Jiangsu Inst Nucl Med, Wuxi 214063, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
FURIN ACTIVITY; LIVING CELLS; IN-VITRO; PROBES; THERAPY; CANCER;
D O I
10.1021/acs.analchem.7b02971
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The design of tumor-targeting, intracellular protease-activatable near-infrared fluorescence (NIRF) nanoprobes is broadly interesting but remains challenging. In this work, we report the rational design of a NIR probe Cys(StBu)Lys(Biotin)-Lys-Lys(Cy5.5)-CBT (1) to facilely prepare the self-quenched nanoparticles 1-NPs for tumor-targeted imaging in vitro and in vivo. The biotinylated 1-NPs could be actively uptaken by biotin receptor-overexpressing tumor cells via receptor-mediated endocytosis. Upon intracellular proteolytic cleavage, 1-NPs were disassembled to yield the small molecular probe Lys(Cy5.5)-Luciferin-Lys(Biotin)-Lys-OH (1-D-cleaved), accompanied by fluorescence "Turn-On". With this NIRF "Turn-On" property, 1-NPs were successfully applied for tumor-targeted imaging. We envision that our nanoparticles could be applied for fluorescence-guided tumor surgery in the near future.
引用
收藏
页码:9625 / 9628
页数:4
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