脱氧核酶
电催化剂
信号(编程语言)
生物传感器
化学
纳米技术
放大器
检出限
磁电机
电化学
对偶(语法数字)
光电子学
材料科学
电极
电压
电气工程
计算机科学
工程类
色谱法
CMOS芯片
物理化学
艺术
文学类
程序设计语言
作者
Jingyi Zhu,Baoshan He,Yao Liu,Yuling Wang,Jinshui Wang,Ying Liang,Huali Jin,Min Wei,Wenjie Ren,Zhiguang Suo,Yiwei Xu
标识
DOI:10.1016/j.bios.2023.115690
摘要
Herein, a novel magneto-mediated electrochemical aptasensor using the signal amplification technologies of DNAzyme motor and electrocatalyst for vanilla (VAN) detection was fabricated. The D/B duplex, formed by the DNAzyme motor that was each silenced by a blocker, and hairpin DNA1 (H1) containing adenosine ribonucleotide (rA) site were tethered on the sites of the gold nanoparticles@hollow porphyrinic-Metal-organic framework/polyethyleneimine-reduced graphene oxide (AuHPCN-222/PEI-rGO)-modified gold electrode (AuE). Then, after homogeneous and specific recognition in the presence of the VAN, trigger DNA was released and enriched by magnetic separation technique and introduced to the sensing platform to activate the DNAzyme motor, which efficiently improved target recognition capability and avoided the obstacle of multiple DNA strands tangling. More interestingly, the activated DNAzyme motor could repeatedly bind to and cleave H1 in the presence of Mg2+, leading to the exposure of a plethora of capture probes. The thionine (Thi) functionalized hairpin DNA2 (H2)–Pt@Ni–Co as signal probes could hybridize with capture probes. Additionally, the Pt@Ni–Co electrocatalysts presented catalytic activity towards Thi to obtain stronger electrochemical signals. VAN with concentrations ranging from 1 × 10−6 to 10 μM was determined and a detection limit was down to 0.15 pM. The designed electrochemical sensor was highly selective with specificity, stability, reproducibility, and reliable capability for monitoring the VAN in real samples.
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