生物传感器
霍乱弧菌
样品(材料)
DNA
生物
色谱法
化学
微生物学
材料科学
细菌
环境化学
纳米技术
遗传学
作者
Md. Romzan Ali,M. S. Bacchu,Md. Ali Ahasan Setu,Selina Akter,MD NAZMUL HASAN,Fahima Chowdhury,Mahbubur Rahman,Md Sohel Ahommed,Md. Zaved Hossain Khan
标识
DOI:10.1016/j.bios.2021.113338
摘要
Due to the epidemics of emerging microbial diseases worldwide, the accurate and rapid quantification of pathogenic bacteria is extremely critical. In this work, a highly sensitive DNA-based electrochemical biosensor has been developed to detect Vibrio cholerae using gold nanocube and 3-aminopropyltriethoxysilane (APTES) modified glassy carbon electrode (GCE) with DNA carrier matrix. Electrochemical impedance spectroscopy (EIS), cyclic voltammetry (CV), Fourier transform infrared spectroscopy (FTIR), scanning electron microscope (SEM) experiments were performed to interrogate the proposed sensor at each stage of preparation. The biosensor has demonstrated high sensitivity with a wide linear response range to target DNA from 10 −8 to 10 −14 ( R 2 = 0.992 ) and 10 −14 to 10 −27 molL −1 ( R 2 = 0.993 ) with a limit of detection (LOD) value of 7.41 × 10 −30 molL −1 ( S/N = 5 ). The biosensor also exhibits a selective detection behavior in bacterial cultures that belong to the same and distant genera. Moreover, the proposed sensor can be used for six consecutive DNA assays with a repeatability relative standard deviations (RSD) value of 5% ( n = 5). Besides, the DNA biosensor shows excellent recovery for detecting V. cholerae in poultry feces, indicating that the designed biosensor could become a powerful tool for pathogenic microorganisms screening in clinical diagnostics, food safety, and environmental monitoring. • A novel electrochemical DNA biosensor is developed for sensitive detection of Vibrio cholerae. • The biosensor has demonstrated high sensitivity with a limit of detection value of 7.41 × 10 −30 molL −1 . • The proposed sensor could be reused for six consecutive DNA assays with a repeatability RSD value of 5%. • This technique might be a promising alternative for monitoring the bacterium in real samples.
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