"Signal-on" SERS sensing platform for highly sensitive and selective Pb2+ detection based on catalytic hairpin assembly

被引:30
作者
Wu, Yan [1 ]
Fu, Cuicui [1 ]
Xiang, Jie [1 ]
Cao, Yulian [1 ]
Deng, Yu [1 ]
Xu, Rui [1 ]
Zhang, Huan [1 ]
Shi, Wenbing [1 ]
机构
[1] Yangtze Normal Univ, Coll Chem & Chem Engn, Chongqing Key Lab Inorgan Special Funct Mat, Chongqing 408100, Peoples R China
基金
中国国家自然科学基金;
关键词
Lead ion detection; Catalytic hairpin assembly; DNAzyme; Surface-enhanced Raman scattering; ENHANCED RAMAN-SPECTROSCOPY; MODIFIED GOLD NANOPARTICLES; FLUORESCENCE DETECTION; COLORIMETRIC DETECTION; PICOMOLAR DETECTION; QUANTUM DOTS; ENZYME-FREE; LEAD IONS; DNA; DNAZYME;
D O I
10.1016/j.aca.2020.06.038
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
In this work, a surface-enhanced Raman scattering (SERS) sensing strategy was proposed for the analysis of lead ion (Pb2+) with high sensitivity and specificity based on the high specificity of the catalytic nucleic acids (DNAzymes) to Pb2+ and the catalytic hairpin assembly (CHA) amplification. First, the Pb2+-DNAzyme initiated the reaction by target Pb2+ and released a linear DNA (rS1). Second, the hairpin DNA 1 (H1) was immobilized on the SERS substrate surface via Ag-S bond. Then, the rS1 could cyclically trigger the allosteric effects of CHA amplification and the H1 was opened and then the R6G-labeled hairpin probe 2 (H2) hybridized with H1 to form H1-H2 double-stranded and the released rS1 could initiate the next cycle of CHA reaction. This process made the Raman tag of R6G close to the surface of SERS substrate, and the intensity of SERS signal from R6G labels increase with the increase of concentration of target Pb2+. Benefiting from outstanding performances of the Pb2+-specific DNAzymes and enzyme-free CHA amplification system, this biosensor exhibits good sensitivity for Pb2+ with a limit of detection of 0.42 pM. More importantly, this developed detection platform could be employed for reliable analysis of Pb2+ in real environment system. (C) 2020 Elsevier B.V. All rights reserved.
引用
收藏
页码:106 / 113
页数:8
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