A "reactive" turn-on fluorescence probe for hypochlorous acid and its bioimaging application

被引:35
作者
Gao, Yunling [1 ,3 ]
Pan, Yong [1 ]
Chi, Yu [1 ]
He, Yuanyuan [2 ]
Chen, Haiyan [2 ]
Nemykin, Victor N. [3 ]
机构
[1] Zhejiang Univ Technol, Coll Chem Engn, State Key Lab Breeding Base Green Chem Synth Tech, Hangzhou 310032, Zhejiang, Peoples R China
[2] China Pharmaceut Univ, Sch Engn, Dept Biomed Engn, Nanjing 210009, Peoples R China
[3] Univ Manitoba, Dept Chem, Winnipeg, MB R3T 2N2, Canada
基金
中国国家自然科学基金; 加拿大自然科学与工程研究理事会;
关键词
aza-BODIPY; Aldoxime; Turn-on probe; Red-emission; AZA-BODIPY DYES; PHOTODYNAMIC THERAPY; LIVING CELLS; SOLAR-CELLS; TRIPLET PHOTOSENSITIZERS; HYDROGEN-PEROXIDE; MYELOPEROXIDASE; CHEMOSENSOR; DERIVATIVES; CHEMODOSIMETER;
D O I
10.1016/j.saa.2018.07.090
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
An aza-BODIPY-CNOH probe attached aldoxime group demonstrated the specific detection for hypochlorous add by the turn-on red emission signal. NMR and HRMS experiments confirmed that the fluorescence originated from the oxidation degradation of the non-fluorescence, aldoxime-based aza-BODIPY-CNOH probe into the red-fluorescence, nitrile oxide-based aza-BODIPY compound aza-BODIPY-CNO. The aza-BODIPY-CNOH probe showed good biocompatibility and was low toxic to living cells as shown from MIT experiments. Living RAW264.7 cells imaging indicated the aza-BODIPY-CNOH probe had good permeability and either exogenous or endogenous HCIO caused the intracellular bright-red fluorescence, showing its potential hypochlorous acid-specific sensing ability in biological systems. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:190 / 196
页数:7
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