化学发光
发光
近红外光谱
费斯特共振能量转移
荧光
自体荧光
纳米传感器
化学
过氧化氢
光化学
材料科学
分析化学(期刊)
光电子学
纳米技术
光学
物理
有机化学
色谱法
作者
Shiyi Zhang,Hao Yuan,Shengchun Sun,Chunlian Qin,Qiming Qiu,Yuyan Feng,Yongjie Liu,Yang Li,Lizhou Xu,Yibin Ying,Ji Qi,Yixian Wang
出处
期刊:Advanced Science
[Wiley]
日期:2023-06-13
卷期号:10 (23): e2207651-e2207651
被引量:32
标识
DOI:10.1002/advs.202207651
摘要
Chemiluminescence (CL) imaging, as an excitation-free technique, exhibits a markedly improved signal-to-noise ratio (SNR) owing to the absence of an excitation light source and autofluorescence interference. However, conventional chemiluminescence imaging generally focuses on the visible and first near-infrared (NIR-I) regions, which hinders high-performance biological imaging due to strong tissue scattering and absorption. To address the issue, self-luminescent NIR-II CL nanoprobes with a second near-infrared (NIR-II) luminescence in the presence of hydrogen peroxide are rationally designed. A cascade energy transfer, including chemiluminescence resonance energy transfer (CRET) from the chemiluminescent substrate to NIR-I organic molecules and Förster resonance energy transfer (FRET) from NIR-I organic molecules to NIR-II organic molecules, occurs in the nanoprobes, contributing to NIR-II light with great efficiency and good tissue penetration depth. Based on excellent selectivity, high sensitivity to hydrogen peroxide, and long-lasting luminescence performance, the NIR-II CL nanoprobes are applied to detect inflammation in mice, showing a 7.4-fold enhancement in SNR compared with that of fluorescence.
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