A 3,5-dinitropyridin-2yl substituted naphthalimide-based fluorescent probe for the selective detection of biothiols and its application in cell-imaging

被引:7
|
作者
Zhuo, Yihua [1 ]
Zhang, Yanyu [1 ]
Feng, Yadong [1 ,2 ]
Xu, Yuqing [3 ]
You, Qihua [1 ,2 ]
Zhang, Lei [4 ]
Huang, Huabin [1 ]
Lin, Lili [1 ,2 ]
机构
[1] Xiamen Huaxia Univ, Coll Environm & Publ Hlth, 288 Tianma Rd, Xiamen 361024, Peoples R China
[2] Fujian Prov Univ, Biochem Pharm Engn Res Ctr, 288 Tianma Rd, Xiamen 361024, Peoples R China
[3] Ludong Univ, Sch Phys & Optoelect Engn, Yantai 264025, Peoples R China
[4] Biol Inst Shanxi, 50 Shifan Rd, Taiyuan 030006, Peoples R China
关键词
SENSITIVE DETECTION; HOMOCYSTEINE; GLUTATHIONE; DESIGN; PLASMA; THIOLS; H2S;
D O I
10.1039/d1ra00010a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A naphthalimide-based fluorescent probe was developed for the sensitive and selective detection of biothiols. The fluorescence of the probe was quenched by the electron-withdrawing 3,5-dinitropyridin-2-yl group via the photoinduced electron transfer process, and turned on by biothiol-triggered nucleophilic aromatic substitution. The sensing mechanism was confirmed by HPLC analysis and theoretical calculations. The probe shows a satisfactory response time of 30 min with low detection limits (Cys: 0.32 mu M; Hcy: 0.88 mu M; GSH: 0.46 mu M). Furthermore, the probe was successfully utilized to detect endogenous and exogenous biothiols in HeLa cells.
引用
收藏
页码:9290 / 9295
页数:6
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