Abstract:a b s t r a c tBacterial food poisoning is an ever-present threat that can be prevented with proper care and handling of food products. A disposable electrochemical immunosensor for the simultaneous measurements of common food pathogenic bacteria namely Escherichia coli O157:H7 (E. coli), campylobacter and salmonella were developed. The immunosensor was fabricated by immobilizing the mixture of anti-E. coli, anticampylobacter and anti-salmonella antibodies with a ratio of 1:1:1 on the surface of the multiwall … Show more
“…This value is markedly smaller than 5000 [20], 3270 cfu/mL [2], 1200 [21], 150 cfu/mL [9], 83.7 cfu/mL [22], 30 cfu/mL [4], and 22 cfu/mL [8], and higher than 7 cfu/mL [23], 3 cfu/mL [24], and 2 cfu/mL [25]. The detection limit of 4.5 fg/ μ L [26] and 800 cells/mL [27] was also realized. The results implied that this detecting approach exhibited a lower detection limit.…”
Silica coated silver (Ag@SiO2) nanoparticles were prepared and characterized by transmission electron microscope (TEM) and UV-vis absorption, and the nanoparticles were used as labels in sandwich-type immunosensor of Escherichia coli O157:H7 (E. coli O157:H7). The labels involved in immunoreaction were dissolved by mixed acid of hydrofluoric acid and nitric acid, and the released Ag+ ions were electrochemical stripping analyzed (via differential pulse voltammetry, DPV) at poly(acrylic acid)/poly(diallyldimethylammonium chloride)/carbon nanotubes (PAA/PDCNT) modified glass carbon electrode (GCE), which obviously enhanced the signal of Ag+ stripping. Then, the number of E. coli O157:H7 could be indirectly reflected by the signal intensity of labeled Ag+. And the results showed that the DPV signals were proportional to the logarithm of the E. coli O157:H7 concentration in the range from 20 cfu/mL to 8.0 × 103 cfu/mL with the detection limit of 13 cfu/mL.
“…This value is markedly smaller than 5000 [20], 3270 cfu/mL [2], 1200 [21], 150 cfu/mL [9], 83.7 cfu/mL [22], 30 cfu/mL [4], and 22 cfu/mL [8], and higher than 7 cfu/mL [23], 3 cfu/mL [24], and 2 cfu/mL [25]. The detection limit of 4.5 fg/ μ L [26] and 800 cells/mL [27] was also realized. The results implied that this detecting approach exhibited a lower detection limit.…”
Silica coated silver (Ag@SiO2) nanoparticles were prepared and characterized by transmission electron microscope (TEM) and UV-vis absorption, and the nanoparticles were used as labels in sandwich-type immunosensor of Escherichia coli O157:H7 (E. coli O157:H7). The labels involved in immunoreaction were dissolved by mixed acid of hydrofluoric acid and nitric acid, and the released Ag+ ions were electrochemical stripping analyzed (via differential pulse voltammetry, DPV) at poly(acrylic acid)/poly(diallyldimethylammonium chloride)/carbon nanotubes (PAA/PDCNT) modified glass carbon electrode (GCE), which obviously enhanced the signal of Ag+ stripping. Then, the number of E. coli O157:H7 could be indirectly reflected by the signal intensity of labeled Ag+. And the results showed that the DPV signals were proportional to the logarithm of the E. coli O157:H7 concentration in the range from 20 cfu/mL to 8.0 × 103 cfu/mL with the detection limit of 13 cfu/mL.
“…ACCEPTED MANUSCRIPT 13 sakazakii were also investigated. The effect of incubation temperature on the ΔIp was studied in the temperature range from 24 to 36 ℃.…”
Section: Accepted Manuscriptmentioning
confidence: 99%
“…Currently, amperometric immunosensor has been widely studied for pathogen detection with convenience and simple preparation [12][13][14][15]. To construct an useful electrochemical immunosensor, working electrode should have large surface areas to load capture molecules, good biocompatibility to preservate biological activity of bimolecular and excellent conductivity to efficiently transport electron [16].…”
“…In the past two decades, label-free alternatives have been studied by many authors. Some of the examples include quartz crystal microbalance (QCM), 1-3 surface acoustic wave (SAW) devices, 4,5 surface plasmon resonance (SPR), 6,7 silicon microcantilevers, [8][9][10][11] electrochemical sensors, [12][13][14] nanotube and nanowire biosensors. [15][16][17] Although these label-free methods can be rapid and simpler, they generally lack the sensitivity of ELISA.…”
In this study, we examined how the materials’ properties of a lead magnesium niobate-lead titanate solid solution, [Pb(Mg1/3Nb2/3)O3]0.63[PbTiO3]0.37 (PMN-PT) piezoelectric plate sensor (PEPS) affected the enhancement of the relative detection resonance frequency shift, −Δf/f of the sensor, where f and Δf were the resonance frequency and resonance frequency shift of the sensor, respectively. Specifically, the electromechanical coupling constant, −k31, of the PMN-PT PEPS was varied by changing the grain size of the piezoelectric layer as well as by applying a bias direct current electric field. Detection of streptavidin at the same concentration was carried out with biotin covalently immobilized on the surface of PEPS. It is shown that the −Δf/f of the same streptavidin detection was increased by more than 2-fold when the −k31 increased from 0.285 to 0.391.
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