A coumarin-based reversible fluorescent probe for Cu2+ and S2- and its applicability in vivo and for organism imaging

被引:9
作者
Lu, Wen [1 ]
Shi, Jiuzhou [1 ]
Chen, Jichao [2 ]
Sun, Lu [1 ]
Shao, Lingcen [1 ]
Ren, Hongyu [1 ]
Huang, Mengmeng [1 ]
Wang, Yanqin [1 ]
Yang, Shilong [3 ]
Li, Xu [1 ]
机构
[1] Nanjing Forestry Univ, Coll Sci, Nanjing 210037, Jiangsu, Peoples R China
[2] Nanjing Forestry Univ, Coll Chem Engn, Nanjing 210037, Jiangsu, Peoples R China
[3] Nanjing Forestry Univ, Adv Anal & Testing Ctr, Nanjing 210037, Jiangsu, Peoples R China
关键词
SEQUENTIAL DETECTION; HYDROGEN-SULFIDE; OXIDATIVE STRESS; AQUEOUS-MEDIA; COPPER; SENSOR; CELLS; ZINC; CHEMOSENSOR; RECOGNITION;
D O I
10.1039/d1nj01951a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This study describes the synthesis of a coumarin-based reversible fluorescent probe BuCAC for the detection of Cu2+ and S2- in CH3CN : PBS (v/v = 8 : 2, pH = 7.4) solution. The resulting BuCAC exhibited high sensitivity (detection limit = 3.03 x 10(-7) M) and selectivity towards Cu2+ through a 2 : 1 binding mode. In the presence of S2-, the BuCAC-Cu2+ recovered to BuCAC and CuS, which in turn perform the function of a sensitive probe with a lower detection limit of about 1.7 x 10(-7) M. This "on-off-on" process can easily occur in 1 min with a repetition of at least 5 times. The sensing mechanism was confirmed by Job's plot analysis, MS, and density theory calculation. Besides, fluorescence imaging in zebrafish, HeLa cells, and soybean root tissue revealed that the probe BuCAC could serve as a valuable tool for monitoring and tracking intracellular Cu2+ and S2- while benefiting from its excellent fluorescence performance and lower cytotoxicity.
引用
收藏
页码:11983 / 11991
页数:9
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