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Sensitive Detection of Hg2+ with Switchable Electrochemiluminescence Luminophore and Disposable Bipolar Electrode
被引:14
作者:
Liu, Hongxing
[1
,2
]
Zhou, Xiaoming
[1
,2
]
Shen, Jinjin
[1
,2
]
Xing, Da
[1
,2
]
机构:
[1] South China Normal Univ, MOE Key Lab Laser Life Sci, Guangzhou 510631, Guangdong, Peoples R China
[2] South China Normal Univ, Inst Laser Life Sci, Coll Biophoton, Guangzhou 510631, Guangdong, Peoples R China
基金:
中国国家自然科学基金;
关键词:
electrochemiluminescence;
label-free detection;
light-switch" molecules;
mercury ions;
paper-based bipolar electrodes;
MERCURY;
NANOCLUSTERS;
SPECTROMETRY;
FLUORESCENT;
CADMIUM;
URINE;
LEAD;
DNA;
D O I:
10.1002/celc.201600912
中图分类号:
O646 [电化学、电解、磁化学];
学科分类号:
081704 ;
摘要:
A novel paper-based bipolar electrode-electrochemiluminescence (pBPE-ECL) switch system was used for the rapid, label-free, and sensitive detection of Hg2+. In the proposed approach, Hg2+ selectively mediates two thymine-enriched single-stranded DNA probes to form double-stranded DNA (dsDNA). In the presence of Hg2+, the "light-switch" molecule [Ru(phen)(2) dppz](2+) can freely intercalate into the base pairs of the dsDNA, resulting in intense ECL emission. The assay takes advantage of the wireless pBPE-ECL platform to yield a low-cost, disposable, and sensitive analysis. The system has a limit of 0.1 nM for Hg2+ detection. We also showed that the system can be used to distinguish Hg2+ over other metal ions, including Pb2+, Zn2+, Cu2+, Ba2+, Co2+, Cd2+, Fe3+, Mn2+, and Li+. Moreover, the proposed approach was rapid, low-cost, and label-free for effective sensing of Hg2+ in drinking and lake water.
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页码:1681 / 1685
页数:5
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