In vivo near-infrared imaging and phototherapy of tumors using a cathepsin B-activated fluorescent probe

被引:97
作者
Chen, Xiaoqiang [1 ,2 ]
Lee, Dayoung [1 ]
Yu, Sungsook [3 ]
Kim, Gyoungmi [1 ]
Lee, Songyi [1 ]
Cho, Yejin [3 ]
Jeong, Haengdueng [3 ]
Nam, Ki Taek [3 ]
Yoon, Juyoung [1 ]
机构
[1] Ewha Womans Univ, Dept Chem & Nano Sci, Seoul 120750, South Korea
[2] Nanjing Tech Univ, Coll Chem Engn, Jiangsu Natl Synerget Innovat Ctr Adv Mat SICAM, State Key Lab Mat Oriented Chem Engn, Nanjing 210009, Jiangsu, Peoples R China
[3] Yonsei Univ, Severance Biomed Sci Inst, Brain Korea PLUS Project Med Sci 21, Coll Med, Seoul 120752, South Korea
基金
新加坡国家研究基金会; 中国国家自然科学基金;
关键词
Specific phototherapy; NIR bioimaging; Enzyme-activated fluorescence; Multiple functional probe; LYSOSOMAL MEMBRANE PERMEABILIZATION; UP-CONVERSION-NANOPARTICLES; PHOTODYNAMIC THERAPY; INDOCYANINE GREEN; CANCER-THERAPY; ALBUMIN; PHOTOSENSITIZER; PROTEASES; APOPTOSIS; DELIVERY;
D O I
10.1016/j.biomaterials.2017.01.020
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The development of multifunctional reagents for simultaneous specific near-infrared (NIR) imaging and phototherapy of tumors is of great significance. This work describes the design of a cathepsin B-activated fluorescent probe (CyA-P-CyB) and its applications as an NIR imaging probe for tumor cells and as a phototherapy reagent for tumors. In vitro experiments demonstrated that CyA-P-CyB was activated via the cleavage of a peptide linker by cathepsin B in tumor cells to produce fluorescence in the NIR region based on a FRET mechanism. MTT assays showed that the phototoxicity of CyA-P-CyB toward cells depended on the activity of cathepsin B, and the probe exhibited specific phototoxicity toward tumor cells. CyA-P-CyB was also successfully applied to the in vivo imaging and phototherapy of tumors. Histological analysis indicated that CyA-P-CyB had no cytotoxic effects on seven mouse tissues (lung, liver, heart, kidney, pancreas, spleen and brain) after the CyA-P-CyB treatment and laser irradiation. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:130 / 140
页数:11
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