Near-infrared multi-functional aggregation-induced emission fluorescent probe for detection of viscosity and peroxynitrite and its imaging application

过氧亚硝酸盐 荧光 光化学 粘度 荧光寿命成像显微镜 化学 分子内力 生物物理学 材料科学 生物化学 有机化学 物理 超氧化物 复合材料 生物 量子力学
作者
Lingzi Zhong,Haiyi Niu,Yanfei Lin,Tianqing Ye,Zheng Shi-yan,Kan Chen,Lei Li,Longhua Guo,Jianbo Wang
出处
期刊:Microchemical Journal [Elsevier BV]
卷期号:206: 111540-111540 被引量:2
标识
DOI:10.1016/j.microc.2024.111540
摘要

Viscosity and peroxynitrite (ONOO−) are two crucial elements that influence the operational status of biological processes within living organisms. Their abnormal changes cause metabolic disorders and even diseases. Therefore, it is important to develop a near-infrared (NIR) probe with an aggregation-induced emission (AIE) feature that is capable of dual channel detection of both viscosity and ONOO−. Here, a NIR fluorescent probe LY with large Stokes shift was synthesized in which triphenylamine was conjugated to a pyridinium phenylborate salt. Probe LY with the distorted intramolecular twisted intramolecular charge transfer (TICT) properties is sensitive to systemic viscosity and exhibits enhanced fluorescence emission at the 704 nm peak. On the other hand, the probe is also susceptible to peroxynitrite-triggered borate oxidation, providing an AIE fluorescence-enhanced response at the 639 nm peak. Moreover, with excellent photochemical stability, lower cytotoxicity and a precise targeting ability for mitochondria, probe LY was used to visualize imaging changes in endogenous and exogenous cellular viscosity and peroxynitrite. The imaging results of the probe during ferroptosis confirmed that both the intracellular viscosity microenvironment and peroxynitrite were further overexpressed. Finally, in vivo imaging experiments showed that the occurrence of inflammation was accompanied by an increase in the viscosity and the release in peroxynitrite.
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