A label-free and ultrasensitive electrochemical biosensor using hybrid polypyrrole/gold nanoelectrocatalyst mediated signal amplification for the detection of miRNA-21

IF 2.7 3区 化学 Q2 CHEMISTRY, ANALYTICAL
LiNa Zhang and YanBin He
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引用次数: 0

Abstract

The quantitative detection of microRNAs (miRNAs) is crucial for the diagnosis of cancers, while the traditional methods involve complicated procedures and restricted signal gain. In this study, we have established an ultrasensitive electrochemical biosensor by combining a target-induced hybridization reaction and signal amplification strategy for the detection of miRNA-21. The signal amplification is achieved through employing double-stranded DNA as scaffolds for methylene blue (MB) and using a polypyrrole@gold nanocomposite (ppy@AuNPs) as the electrochemical catalyst for further enhancing the signal. Therefore, this proposed electrochemical platform displayed an analytical performance with a wide linear range from 10 fM to 100 nM and a low detection limit down to 5.4 fM. The excellent selectivity allows the biosensor to discriminate miRNA-21 from other miRNAs, even the one base-mismatched sequence. Moreover, this nanoelectrocatalyst-based platform exhibited good reproducibility and remarkable storage stability, which shows great potential for miRNA-21 detection.

Abstract Image

利用混合聚吡咯/金纳米电催化剂介导的信号放大技术检测 miRNA-21 的无标记超灵敏电化学生物传感器。
微RNA(miRNA)的定量检测对癌症诊断至关重要,而传统方法程序复杂、信号增益有限。在这项研究中,我们结合靶诱导杂交反应和信号放大策略,建立了一种超灵敏的电化学生物传感器,用于检测 miRNA-21。信号放大是通过使用双链 DNA 作为亚甲基蓝(MB)的支架,并使用聚吡咯@金纳米复合材料(ppy@AuNPs)作为电化学催化剂进一步增强信号来实现的。因此,该电化学平台的分析性能优异,线性范围从 10 fM 到 100 nM,检测限低至 5.4 fM。出色的选择性使该生物传感器能够区分 miRNA-21 和其他 miRNA,甚至是一个碱基不匹配的序列。此外,这种基于纳米电催化剂的平台表现出良好的重现性和显著的储存稳定性,显示出在 miRNA-21 检测方面的巨大潜力。
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来源期刊
Analytical Methods
Analytical Methods CHEMISTRY, ANALYTICAL-FOOD SCIENCE & TECHNOLOGY
CiteScore
5.10
自引率
3.20%
发文量
569
审稿时长
1.8 months
期刊介绍: Early applied demonstrations of new analytical methods with clear societal impact
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