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基于计时安培法的活快速定量检测。

Rapid Quantitative Detection of Live Based on Chronoamperometry.

机构信息

School of Environmental and Chemical Engineering, Xi'an Polytechnic University, Xi'an 710600, China.

Tianjin Institute of Environmental Medicine and Operational Medicine, Tianjin 300050, China.

出版信息

Biosensors (Basel). 2022 Oct 8;12(10):845. doi: 10.3390/bios12100845.

Abstract

The rapid quantitative detection of Escherichia coli (E. coli) is of great significance for evaluating water and food safety. At present, the conventional bacteria detection methods cannot meet the requirements of rapid detection in water environments. Herein, we report a method based on chronoamperometry to rapidly and quantitatively detect live E. coli. In this study, the current indicator i0 and the electricity indicator A were used to record the cumulative effect of bacteria on an unmodified glassy carbon electrode (GCE) surface during chronoamperometric detection. Through the analysis of influencing factors and morphological characterization, it was proved that the changes of the two set electrochemical indicator signals had a good correlation with the concentration of E. coli; detection time was less than 5 min, the detection range of E. coli was 104−108 CFU/mL, and the error range was <30%. The results of parallel experiments and spiking experiments showed that this method had good repeatability, stability, and sensitivity. Humic acid and dead cells did not affect the detection results. This study not only developed a rapid quantitative detection method for E. coli in the laboratory, but also realized a bacterial detection scheme based on the theory of bacterial dissolution and adsorption for the first time, providing a new direction and theoretical basis for the development of electrochemical biosensors in the future.

摘要

快速定量检测大肠杆菌(E. coli)对于评估水和食品安全具有重要意义。目前,常规的细菌检测方法无法满足水环境中快速检测的要求。在此,我们报道了一种基于计时安培法快速定量检测活大肠杆菌的方法。在本研究中,使用电流指示剂 i0 和电量指示剂 A 记录了在计时安培检测过程中细菌在未经修饰的玻碳电极(GCE)表面上的累积效应。通过对影响因素和形态特征的分析,证明了两种电化学指示剂信号的变化与大肠杆菌浓度具有良好的相关性;检测时间小于 5 分钟,大肠杆菌的检测范围为 104-108 CFU/mL,误差范围小于 30%。平行实验和加标实验的结果表明,该方法具有良好的重现性、稳定性和灵敏度。腐殖酸和死细胞不会影响检测结果。本研究不仅开发了一种大肠杆菌的实验室快速定量检测方法,而且首次实现了基于细菌溶解和吸附理论的细菌检测方案,为未来电化学生物传感器的发展提供了新的方向和理论依据。

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