化学
适体
检出限
脱氧核酶
电极
电化学
组合化学
劈理(地质)
线性范围
黄曲霉毒素
生物传感器
寡核苷酸
纳米技术
劈开
信号(编程语言)
纳米复合材料
纳米颗粒
核苷酸
电化学气体传感器
纳米材料
胶体金
荧光
纳米点
脱氧核糖核酸酶
滚动圆复制
作者
Xiaodong Lü,Xinyi Liu,Qiaodie Wang,Xiaoze Dong,Mingwei Qin,Gengli Huang,Xiang Han,Yi-Yao Wu,Zhouping Wang
标识
DOI:10.1021/acs.analchem.5c05580
摘要
Designing an electrochemical aptasensor for detecting Aflatoxin B1 (AFB 1 ) in food samples is a great challenge. Herein, a catalytic hairpin assembly combined with a bipedal Mg 2+ -dependent deoxyribonuclease (Mg 2+ -DNAzyme) serves as a signal enhancer. Polyethylenimine-Ce-based metal–organic framework@nitrogen-doped multiwalled carbon nanotubes/gold nanoparticles nanocomposites (P-CeMOFs@MWCNTs/AuNPs) were used as electrode modification materials, and MOF-derived Co 3 O 4 and AuNP-labeled oligonucleotides (Au@Co 3 O 4 @S) served as signal probes. An ultrasensitive electrochemical aptasensor for the detection of AFB 1 was developed. During the reaction, AFB 1 displaced the aptamer from the complementary chain (T), enabling formation of the HP1-HP2 complex by opening HP1 and binding to HP2. HP3, containing ribonucleotide (rA), was repeatedly cleaved in the presence of Mg 2+, thereby vacating the complementary chain to capture the Au@Co 3 O 4 @S signal probe, ultimately leading to signal amplification. With such a design, the detection range of the sensor was verified to be 1 × 10 –4 –1 × 10 2 ng/mL, and the limit of detection was 6.3 × 10 –5 ng/mL. Under optimal conditions, the aptasensor had excellent specificity, reproducibility, and stability, while the recovery in food samples made it eligible for a wide range of applications.
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