化学
荧光
体内
过氧化氢
生物物理学
内生
检出限
分子内力
近红外光谱
炎症
临床前影像学
光化学
生物化学
立体化学
免疫学
光学
生物
物理
生物技术
色谱法
作者
Jingli Hou,Meng Qian,Huanhuan Zhao,Yingchun Li,Yongfang Liao,Guifang Han,Zhelong Xu,Feng Wang,Yuguang Song,Yangping Liu
标识
DOI:10.1016/j.aca.2018.03.028
摘要
Much attention has been paid to develop optical probes for noninvasive, quantitative, in vivo monitoring of hydrogen peroxide (H2O2) due to its important roles in the initiation and development of numerous diseases. Motivated to meet this need, we herein report the synthesis of a near-infrared (NIR) fluorescent probe (AB1) for H2O2 by modulating intramolecular charge transfer (ICT) process of the dye 9H-1,3-Dichloro-7-hydroxy-9,9-dimethylacridine-2-one (DDAO). The probe AB1 exhibits both a large NIR fluorescence turn-on and a ratiometric response to H2O2 with high sensitivity and specificity. The fluorescence response of AB1 has a good linear relationship with H2O2 over a wide concentration range from 1 μM to 100 μM, thus affording a detection limit of 0.42 μM. Confocal microscopic experiments demonstrated that AB1 could ratiometrically detect exogenous and endogenous H2O2 in living cells. Moreover, owing to the NIR emission of DDAO, the probe was also utilized to image endogenous H2O2 from the peritoneal cavity in a mouse model of lipopolysaccharide-induced acute inflammation, based on the fluorescence turn-on mode. This new probe shows great potential as a reliable chemical tool to study the development and progression of H2O2-associated diseases in living animals.
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