Dual enzyme-free amplification strategy for ultra-sensitive fluorescent detection of bisphenol A in water

被引:27
作者
Yun, Wen [1 ]
Wu, Hong [1 ]
Chen, Lin [3 ,4 ]
Yang, Lizhu [2 ]
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
[4] Southwest Univ Sci & Technol, Sch Mat Sci & Engn, Mianyang 621010, Peoples R China
基金
中国国家自然科学基金;
关键词
Bisphenol A; AuNPs; Hybridization chain reaction; Fluorescent; Enzyme-strand recycling; Enzyme-free; HYBRIDIZATION CHAIN-REACTION; COLORIMETRIC DETECTION; GOLD NANOPARTICLES; CARBON; APTASENSOR; MIGRATION; SAMPLES; FOOD; BPA;
D O I
10.1016/j.aca.2018.02.064
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
An ultra-sensitive strategy for bisphenol A (BPA) detection based on dual enzyme-free strategies: hybridization chain reaction (HCR) and enzyme-strand recycling reaction has been developed. The BPA aptamer can form hairpins structure by the partly self-complementary sequence. In the presence of BPA, the released BPA aptamer sequence can trigger the HCR between two hairpins to from a long nicked double-helix DNA. The tails of hairpins on the duplex DNA were closely enough to hybridize with molecular beacon (MB) on the gold nanoparticles (AuNPs) to circularly cleave the loop of MB, leading to a "turn-on" fluorescent signal. This method exhibited high sensitivity for BPA detection in a linear rang from 0.2 to 1000 pM with 0.05 pM of limit of detection. Moreover, it was successfully used for BPA detection in real water samples. Importantly, this method was simple without complex enzymatic procedure and high cost, showing a promising future for on-site detection of BPA in practical application. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:104 / 109
页数:6
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