生物医学中的光声成像
体内
荧光
化学
荧光寿命成像显微镜
临床前影像学
生物物理学
纳米技术
材料科学
光学
生物
物理
量子力学
生物技术
作者
Bangping Hu,Qi Liu,Yulan Jiang,Yujie Huang,Haiwei Ji,Jiqi Zhang,Xia Wang,Xing‐Can Shen,Hua Chen
出处
期刊:Angewandte Chemie
[Wiley]
日期:2024-11-13
卷期号:64 (7): e202418378-e202418378
被引量:22
标识
DOI:10.1002/anie.202418378
摘要
Abstract Hydrogen persulfide (H 2 S 2 ) plays a significant role in redox biology and signal transduction; therefore, quantitative visualization of H 2 S 2 in the deep tissue of living organisms is essential for obtaining reliable information about relevant pathophysiological processes directly. However, currently reported H 2 S 2 probes are unsuitable for this purpose because of their poor selectivity for many polysulfide species or their short wavelength, which hinders precise imaging in deep tissues. Herein, for the first time, we report a unique H 2 S 2 ‐mediated dithiole formation reaction. Based on this reaction, we construct the first NIR‐II fluorescence (FL) and photoacoustic (PA) dual‐ratiometric probe ( NIR‐II‐H 2 S 2 ) for quantitatively visualizing H 2 S 2 in vivo. This probe shows dual‐ratiometric NIR‐II fluorescence (I 840 /I 1000 , 107‐fold) and photoacoustic (PA 800 /PA 900 , 6.5‐fold) responses towards Na 2 S 2 species with high specificity, excellent sensitivity (1.8 nM), improved water solubility, and deep‐tissue penetration. More importantly, using NIR‐II dual‐ratiometric FL/PA imaging, we successfully demonstrated that the probe could be used to accurately quantify the fluctuating H 2 S 2 levels in the liver‐injury mouse models induced by lipopolysaccharides or metformin drugs. Overall, this study not only presents a promising tool for H 2 S 2 ‐related pathological research, but also provides a unique recognition site that may be generalized for designing more useful H 2 S 2 imaging agents in the future.
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