A microfluidic impedance biosensor based on immunomagnetic separation and urease catalysis for continuous-flow detection of E-coli O157:H7

被引:69
|
作者
Yao, Lan [1 ]
Wang, Lei [2 ]
Huang, Fengchun [2 ]
Cai, Gaozhe [2 ]
Xi, Xinge [3 ]
Lin, Jianhan [1 ,2 ]
机构
[1] China Agr Univ, Key Lab Agr Informat Acquisit Technol, Minist Agr, Beijing 100083, Peoples R China
[2] China Agr Univ, Key Lab Modern Precis Agr Syst Integrat Res, Minist Educ, Beijing 100083, Peoples R China
[3] Univ Arkansas, Dept Biol & Agr Engn, Fayetteville, AR 72701 USA
关键词
Impedance biosensor; Impedance normalization; Continuous-flow detection; Immunomagenatic separation; Urease catalysis; RAPID DETECTION; MAGNETIC NANOPARTICLES; SIGNAL AMPLIFICATION; SENSITIVE DETECTION; IMMUNOSENSOR; MICROELECTRODE; SAMPLES; SYSTEM;
D O I
10.1016/j.snb.2017.12.110
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Early screening of foodborne pathogens is a key to control the outbreaks of foodborne illnesses. In this study, a microfluidic impedance biosensor combined with the immune magnetic nanoparticles (MNPs) for bacteria separation, the urease for biological signal amplification and the microfluidic chip for impedance measurement was developed for rapid, sensitive and continuous-flow detection of E. coli O157:H7. After the streptavidin modified MNPs were conjugated with the biotinylated polyclonal antibodies (PAbs) to form the immune MNPs, the target bacteria was first separated by the MNPs from the background to form the MNP-bacteria complexes. Then, the gold nanoparticles (GNPs) modified with the urease and the aptamers against E. coli O157:H7 were conjugated with the MNP-bacteria to form the MNP-bacteria-GNP-urease complexes. Finally, the complexes were used to catalyze the hydrolysis of urea into ammonium carbonate, leading to the decrease in the impedance. The impedance was online measured by this proposed biosensor and analyzed using the impedance normalization to determine the concentration of E. coli O157:H7. A good linear relationship between the impedance relative change rate of the catalysate and the concentration of the bacteria was obtained with low detection limit of 12 CFU/mL. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:1013 / 1021
页数:9
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