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基于 EXO III 驱动的信号放大的荧光和极性可切换光电化学双模均相传感平台用于超灵敏庆大霉素检测。

Fluorescent and polarity-switchable photoelectrochemical dual-mode homogeneous sensing platform for ultrasensitive kanamycin detection based on EXO III-driven signal amplification.

机构信息

Hubei Key Laboratory of Processing and Application of Catalytic Materials, College of Chemistry and Chemical Engineering, Huanggang Normal University, Huanggang, 438000, China.

School of Chemistry and Chemical Engineering, Yancheng Institute of Technology, Yancheng, 224051, China.

出版信息

Mikrochim Acta. 2024 Sep 16;191(10):602. doi: 10.1007/s00604-024-06679-5.

Abstract

A fluorescent and photoelectrochemical (PEC) dual-mode biosensor based on target biorecognition-triggered cyclic amplification was constructed for Kana detection. With the assistance of the catalyzed reaction of exonuclease III, a Kana-aptamer DNA duplex was designed for conducting the cyclic release of G-rich DNA sequence as well as output DNA S2. The released G-rich sequence triggers the fluorescence (FL) of thioflavin T (ThT), the intensity of which is positively correlated with the Kana concentration. The linear range is 0.2 to 30 nM, and the detection limit reaches 0.07 nM. Simultaneously, the released output DNA S2 was captured by FeO@CdTe-probe ssDNA and then combined with methylene blue to realize the transduction of polarity-reversed PEC signal, leading to the sensitive detection of Kana with a linear range of 0.2 to 40 nM and a calculated detection limit of 0.2 nM. The outstanding performance endows the dual-mode biosensor a promising prospect for practical application.

摘要

基于目标生物识别触发循环扩增的荧光和光电化学(PEC)双模生物传感器被构建用于检测卡那霉素。在核酸外切酶 III 的催化反应的辅助下,设计了一种卡那霉素适体 DNA 双链体,用于循环释放富含 G 的 DNA 序列和输出 DNA S2。释放的富含 G 的序列触发了硫黄素 T(ThT)的荧光(FL),其强度与卡那霉素浓度呈正相关。线性范围为 0.2 至 30 nM,检测限达到 0.07 nM。同时,释放的输出 DNA S2 被 FeO@CdTe-探针 ssDNA 捕获,然后与亚甲基蓝结合,实现极性反转 PEC 信号的转导,从而实现对卡那霉素的灵敏检测,线性范围为 0.2 至 40 nM,计算检测限为 0.2 nM。出色的性能使双模生物传感器具有广阔的实际应用前景。

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