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A biomarker (ONOO-)-activated multicolor fluorescent probe for early detection and assessment of arthritis
被引:41
作者:
Xu, Weizhen
[1
]
Yang, Qiaomei
[1
]
Zeng, Jiaqi
[2
]
Tan, Libin
[1
]
Zhou, Liyi
[1
]
Peng, Longpeng
[1
]
Zhou, Yizhuang
[2
]
Xie, Can
[1
]
Luo, Kun
[1
]
Zhang, Zhen
[3
]
机构:
[1] Cent South Univ Forestry & Technol, Coll Food Sci & Engn, Changsha 410004, Hunan, Peoples R China
[2] Guilin Med Univ, Sch Publ Hlth, Guangxi Key Lab Environm Expos & Entire Lifecycle, Guilin 541001, Guangxi, Peoples R China
[3] Shandong Univ Tradit Chinese Med, Innovat Res Inst Tradit Chinese Med, Jinan, Shandong, Peoples R China
来源:
SENSORS AND ACTUATORS B-CHEMICAL
|
2022年
/
359卷
关键词:
Fluorescent probe;
Multicolor imaging;
ONOO--activated;
Rat imaging;
Peroxynitrite (ONOO-);
RHEUMATOID-ARTHRITIS;
FLUOROGENIC PROBES;
HYPOCHLOROUS ACID;
PEROXYNITRITE;
CELLS;
DNA;
MITOCHONDRIA;
TRACKING;
MODEL;
D O I:
10.1016/j.snb.2022.131565
中图分类号:
O65 [分析化学];
学科分类号:
070302 ;
081704 ;
摘要:
To understand the entangled relationship between reactive oxygen species (ROS) and arthritis, it is of great interest to urgently need an effective bioanalytical method to detect biomarker peroxynitrite (ONOO-) of arthritis in vivo. In contrast to the previously reported ONOO- fluorescent probes, multicolor fluorescent probe could be applied to complex environments for multi-component analysis and provide multichannel imaging results. However, multicolor fluorescent probes for ONOO- detecting have not been reported so far. Herein, an ONOO-- activated multicolor fluorescent probe (MULTI-ONOO) based on FRET was developed for quantitative detecting and visualization of ONOO- levels in arthritis. This probe mainly contained an acceptor (near-infrared xanthane fluorophore) and a donor (naphthalimide fluorophore). In the presence of ONOO-, the oxonium ion undergoes a strong nucleophilic response between ONOO- and xanthane to generate coumarin (CM) and naphthimide (NP) fluorophores with multicolor signal output. Impressively, MULTI-ONOO has a rapid response time (~20 s) and outstanding detection limits as low as 11.6 nM. Finally, this probe was successfully adopted to detect endogenous ONOO- in living cells, arthritis tissues and rat model. Thus, this ONOO--activated multicolor probe could provide a robust tool for investigating the role of ONOO- between in different inflamed diseases.
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页数:8
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