A “turn-off” SERS aptasensor based DNAzyme-gold nanorod for ultrasensitive lead ion detection

被引:18
|
作者
Xu W. [1 ,2 ,3 ]
Zhao A. [1 ,2 ,3 ]
Zuo F. [1 ,2 ,3 ]
Jafar Hussain H.M. [4 ]
Khan R. [4 ]
机构
[1] Institute of Intelligent Machines, Chinese Academy of Sciences, Hefei
[2] Department of Chemistry, University of Science and Technology of China, Hefei, 230026, Anhui
[3] State Key Laboratory of Transducer Technology, Chinese Academy of Sciences, Hefei
[4] School of Life Sciences, University of Science and Technology of China, Hefei
来源
基金
中国国家自然科学基金;
关键词
Complex biological samples; DNAzyme; Gold nanorods; Lead (II) ions; Sensitivity; Surface-enhanced Raman scattering;
D O I
10.1016/j.acax.2019.100020
中图分类号
学科分类号
摘要
It is great significance to precisely monitor lead (II) ions (Pb2+) for environment protection and human health monitoring. We designed a sensitive detection strategy for sensitive and selective determination of Pb2+, based on a Pb2+-specific DNAzyme as the catalytic unit, Cy3-labeled DNA modified gold nanorods (AuNRs) as SERS reporter. Firstly, AuNRs surface were employed as a platform for the immobilization of thiolated probe DNA, and then hybridized with DNAzyme catalytic beacons. By taking advantage of DNAzyme digest, a molecular beacon, causes a “turn-off” SERS signal by disrupting the labeled probes. Under the optical conditions, the DNAzyme-AuNRs sensor system exhibited high sensitivity, acceptable stability and reproducibility with a wide linear range from 0.5 to 100 nM (R2 = 0.9973), and an ultra-low detection limit of 0.01 nM. The proposed strategy has additional advantages of being less time-consuming, low-cost and remote query, and avoids the interference of some metals such as Fe3+, Cd2+, Ba2+, Cu2+, Zn2+. The SERS biosensor system has been successfully applied for detecting Pb2+ in real samples with a satisfactory result. The result indicated that the proposed sensing strategy not only enriches SERS platform of monitoring Pb2+ but also exhibits potential for the point-of-care diagnostic application of the clinical screening in complicated biological samples. © 2019
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