菁
费斯特共振能量转移
自体荧光
近红外光谱
荧光
体内
化学
荧光寿命成像显微镜
临床前影像学
光化学
材料科学
光学
物理
生物技术
生物
作者
Lei Shan,Kejia Jiang,Chenqing Zhang,Wei Sun,Yuantao Pan,Dong Wang,Peng Huang,Jing Lin
出处
期刊:Research
[American Association for the Advancement of Science]
日期:2023-01-01
卷期号:6
被引量:9
标识
DOI:10.34133/research.0286
摘要
Second near-infrared (NIR-II) window optical molecular imaging kicks off a new revolution in high-quality imaging in vivo, but always suffers from the hurdles of inevitable tissue autofluorescence background and NIR-II probe development. Here, we prepare a Förster resonance energy transfer-based ratiometric NIR-II window hydrogen sulfide (H 2 S) sensor through the combination of an H 2 S-responsive NIR-II cyanine dye (acceptor, LET-1055) and an H 2 S-inert rhodamine hybrid polymethine dye (donor, Rh930). This sensor not only exhibits high sensitivity and selectivity, but also shows rapid reaction kinetics (~20 min) and relatively low limit of detection (~96 nM) toward H 2 S, allowing in vivo ratiometric NIR-II fluorescence imaging of orthotopic liver and colon tumors and visualization of the drug-induced hepatic H 2 S fluctuations. Our findings provide the potential for advancing the feasibility of NIR-II activity-based sensing for in vivo clinical diagnosis.
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