化学
线性
整改
电阻式触摸屏
分析物
纳米孔
离子键合
分析化学(期刊)
光电子学
纳米技术
生物系统
离子
色谱法
电压
电子工程
材料科学
计算机科学
物理
有机化学
量子力学
计算机视觉
生物
工程类
作者
Xian Zhang,Zeng‐Qiang Wu,You‐Wei Zheng,Juan Song,Weiwei Zhao,Jing‐Juan Xu
标识
DOI:10.1021/acs.analchem.4c00629
摘要
As two mainstream ionic detection techniques, ionic current rectification (ICR) suffers from large fluctuations in trace level detection, while resistive-pulse sensing (RPS) encounters easy clogs in high-concentration detection. By rationally matching the nanopore size with the DNA tetrahedron (TDN), this work bridges the two techniques to achieve reliable detection with wide linearity. As a representative analyte, miRNA-10b could specifically combine with and release TDN from the interior wall, which thus induced the simultaneous generation of distinct ICR and RPS signals. The ICR signals could be attributed to the balance between the effective orifice and surface charge density of the inner wall, while the RPS signals were induced by the complex of miRNA-10b and TDN passing through the nanopore. Such an operation contributed to a wide detection range of 1 fM-1 nM with a good linearity. The feasibility of this method is also validated in single-cell and real plasma detection.
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