A time-resolved near-infrared phosphorescent iridium(iii) complex for fast and highly specific peroxynitrite detection and bioimaging applications

被引:35
|
作者
Li, Yuanyan [1 ,2 ]
Wu, Yongquan [2 ,3 ]
Chen, Luyan [2 ]
Zeng, Hong [2 ]
Chen, Xiaoyong [2 ]
Lun, Weican [2 ]
Fan, Xiaolin [1 ,2 ]
Wong, Wai-Yeung [3 ,4 ]
机构
[1] Nanchang Univ, Coll Chem, 999 Xuefu Ave, Nanchang 330031, Jiangxi, Peoples R China
[2] Gannan Normal Univ, Sch Chem & Chem Engn, Ganzhou 341000, Peoples R China
[3] Hong Kong Polytech Univ, Dept Appl Biol & Chem Technol, Hung Hom, Hong Kong, Peoples R China
[4] Hong Kong Polytech Univ, Shenzhen Res Inst, Shenzhen 518057, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
FLUORESCENT-PROBE; ENDOGENOUS PEROXYNITRITE; LIVING CELLS; INFLAMMATION; MITOCHONDRIA; AGGREGATION; VISCOSITY; SELENIUM;
D O I
10.1039/c9tb01673b
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Peroxynitrite (ONOO-), one of the reactive oxygen/nitrogen species (ROS/RNS) found in vivo, plays crucial roles in many physiological and pathological processes. The ability to selectively and sensitively determine ONOO(-)in vivo is important for the understanding of its biological roles. Thus, by utilizing the excellent chemical stability and photostability, high luminescence efficiency, and long luminescence lifetime of iridium complexes, we developed a novel near-infrared (NIR) phosphorescent iridium(iii) complex (FNO2) probe to detect ONOO- within seconds. The probe FNO2 showed better selectivity towards ONOO- over other interfering biomolecules, including O-2(-) and ClO-. Moreover, it possessed a long luminescence lifetime, which enabled successful elimination of the interference from background fluorescence in vitro (simulated by Rhodamine B) in time-resolved emission spectra. Finally, in addition to its low cytotoxicity, the probe FNO2 showed emission wavelength in the NIR region and was able to specifically sense ONOO- induced in living cells and inflamed mouse models.
引用
收藏
页码:7612 / 7618
页数:7
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