A unique off-on near-infrared QCy7-derived probe for selective detection and imaging of hydrogen sulfide in cells and in vivo

被引:24
作者
Su, Dongdong [1 ]
Cheng, Dan [2 ]
Lv, Yun [2 ]
Ren, Xiaojun [1 ]
Wu, Qian [2 ]
Yuan, Lin [2 ]
机构
[1] Beijing Univ Technol, Dept Chem & Chem Engn, Beijing 100124, Peoples R China
[2] Hunan Univ, Coll Chem & Chem Engn, State Key Lab Chemo Biosensing & Chemometr, Changsha 410082, Hunan, Peoples R China
基金
中国国家自然科学基金;
关键词
Fluorescent probe; Hydrogen sulfide; Fluorescence spectroscopy; Near-infrared; Off-on; In vivo; RATIOMETRIC FLUORESCENT-PROBE; CYANINE-BASED PROBE; SULFUR; H2S; FLUOROPHORE; ELECTRODE; GATEWAY; DISEASE; DESIGN; LEVEL;
D O I
10.1016/j.saa.2019.117635
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
Hydrogen sulfide (H2S) has been found to be an important biological regulator that plays important roles in many physiological and pathological processes. Near-infrared (NIR) fluorescent probes capable of selectively detecting H2S in vivo will be useful tools to understand its mechanisms in biological processes. Herein, we reported an easily synthesized and stimuli-responsive NIR fluorescent probe (QCy7-HS) for selective evaluation of endogenous H2S in the living cells and mice. In response to cellular H2S stimulus, QCy7-HS is converted to (tCy7 and shows a unique off-on near-infrared fluorescence signal change. The results of selectivity and kinetic studies indicated that our probe has high H2S binding capacity. Therefore, this probe was used for the fluorescence detection of H2S in cells. Moreover, the probe was applied for study exogenous and endogenous H2S in live mice, indicating that the new probe can be used as an efficient tool on H2S related events in living animals. (C) 2019 Elsevier B.V. All rights reserved.
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页数:7
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