A dynamic, ultra-sensitive and "turn-on" strategy for fluorescent detection of uranyl based on DNAzyme and entropy-driven amplification initiated circular cleavage amplification

被引:23
作者
Yun, Wen [1 ,3 ]
Wu, Hong [1 ]
Yang, Zhehan [1 ]
Wang, Ruiqi [1 ]
Wang, Chongjun [1 ]
Yang, Lizhu [2 ]
Tang, Yongjian [3 ]
机构
[1] Chongqing Technol & Business Univ, Coll Environm & Resources, Chongqing Key Lab Catalysis & New Environm Mat, Chongqing 400067, Peoples R China
[2] Wenzhou Med Univ, Sch Pharmaceut Sci, Wenzhou 325035, Zhejiang, Peoples R China
[3] Southwest Univ Sci & Technol, State Key Lab Environm Friendly Energy Mat, Mianyang 621010, Peoples R China
基金
中国国家自然科学基金;
关键词
Fluorescence; Uranyl; DNAzyme; Entropy-driven amplification; Circular cleavage; ELECTROCHEMICAL BIOSENSOR; DEPLETED URANIUM; COLORIMETRIC DETECTION; SIGNAL AMPLIFICATION; ICP-MS; RECOGNITION; RATIOS; SENSOR; STEP; HG2+;
D O I
10.1016/j.aca.2019.04.018
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A uranyl detection strategy with ultra-sensitivity was developed based on entropy-driven amplification and DNAzyme circular cleavage amplification. The cleavage of UO22+-specific DNAzyme produces a DNA fragment to initiate the entropy-driven amplification. Two DNA sequences released from the entropy-driven amplification are partly complementary. They can form an entire enzyme strand (E-DNA) of Mg2+-specific DNAzyme. The formed E-DNA can circularly cleave FAM-labeled probes on gold nanoparticles (AuNPs), causing the leaving of FAM from AuNPs and recovery of fluorescent signal. A linear relationship was obtained in the range from 30 pM to 5 nM between fluorescence intensity and concentration of UO22+. The limit of detection was low to 13 pM. This method showed a promising future for practical application in real water samples. (C) 2019 Elsevier B.V. All rights reserved.
引用
收藏
页码:104 / 110
页数:7
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