Dual-signal Amplification Strategy Aptasensor Based on Exonuclease III and Ordered Mesoporous Carbon-Gold Nanocomposites for Tetracycline Detection in Milk

被引:4
|
作者
Liu, Zengning [1 ,2 ]
Xu, Qingcui [1 ,2 ]
Fu, Jiayun [1 ,2 ]
Shi, Zhaoqiang [1 ,2 ]
Yang, Qingqing [1 ,2 ]
Guo, Yemin [1 ,2 ]
Zhang, Yanyan [1 ,2 ]
Sun, Xia [1 ,2 ]
Wang, Zhiqiang [2 ,3 ]
机构
[1] Shandong Univ Technol, Sch Agr Engn & Food Sci, 12 Zhangzhou Rd, Zibo 255049, Shandong, Peoples R China
[2] Shandong Prov Engn Res Ctr Vegetable Safety & Qua, 12 Zhangzhou Rd, Zibo 255049, Shandong, Peoples R China
[3] Shandong Univ Technol, Coll Comp Sci & Technol, 12 Zhangzhou Rd, Zibo 255049, Shandong, Peoples R China
来源
INTERNATIONAL JOURNAL OF ELECTROCHEMICAL SCIENCE | 2018年 / 13卷 / 08期
基金
中国国家自然科学基金;
关键词
Aptasensor; Screen-printed carbon electrodes; Ordered mesoporous carbon; Tetracycline residues; Real-time field detection; TANDEM MASS-SPECTROMETRY; LIQUID-CHROMATOGRAPHY; COLORIMETRIC APTASENSOR; SENSITIVE DETECTION; DNA APTAMER; IN-VITRO; BIOSENSOR; NANOPARTICLES; ELECTRODE; ACETYLCHOLINESTERASE;
D O I
10.20964/2018.08.120
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
In this paper, a screen-printed aptasensor based on a dual-signal amplification strategy with enzyme assisted target circulation and modification with ordered mesoporous carbon (OMC)-gold nanoparticle (AuNP) nanocomposites was used to detect tetracycline (TET) in milk. Exonuclease III (Exo III), an enzyme, is known to recognize double-stranded DNA nonspecifically. To take advantage of this intrinsic property, Exo III was selected to facilitate the target circulation and amplify the signal. Furthermore, OMC and AuNP nanocomposites formed a unique sensing film with a large surface area and good electronic conductivity, amplifying the current signal for tetracycline detection with excellent sensitivity. A TET-binding aptamer was self-assembled onto the surface of screen-printed carbon electrodes (SPCEs) modified with the nanocomposites to form a sensing layer. Additionally, Exo III sheared the hybridized double chain selectively, releasing the tetracycline target. The released target and the remaining hairpin probe hybridized again. After each cycle of digestion, the target was recycled, leading to amplification. Moreover, real milk samples were directly measured after diluting the milk 3 times. The results showed that the present dual-signal amplification strategy for tetracycline analysis exhibited a detection limit of 3.0 mu g/L with high specificity and demonstrated its applicability for detecting tetracycline residues in milk samples.
引用
收藏
页码:8260 / 8274
页数:15
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