2020
DOI: 10.1007/s00216-020-02417-x
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Probing antibody surface density and analyte antigen incubation time as dominant parameters influencing the antibody-antigen recognition events of a non-faradaic and diffusion-restricted electrochemical immunosensor

Abstract: Electrochemical sensors based on antibody-antigen recognition events are commonly used for the rapid, label-free, and sensitive detection of various analytes. However, various parameters at the bioelectronic interface, i.e., before and after the probe (such as an antibody) assembly onto the electrode, have a dominant influence on the underlying detection performance of analytes (such as an antigen). In this work, we thoroughly investigate the dependence of the bioelectronic interface characteristics on paramet… Show more

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Cited by 26 publications
(17 citation statements)
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References 26 publications
(29 reference statements)
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“…Moreover, the conformational change of the antibody–antigen complex may also play a role in the signal-on mechanism of the sensor, as it can give more access to the redox molecules to the surface, enhancing the electron transfer. Tunable signal-off and signal-on electrochemical sensors have been previously reported. , …”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…Moreover, the conformational change of the antibody–antigen complex may also play a role in the signal-on mechanism of the sensor, as it can give more access to the redox molecules to the surface, enhancing the electron transfer. Tunable signal-off and signal-on electrochemical sensors have been previously reported. , …”
Section: Resultsmentioning
confidence: 99%
“…Tunable signal-off and signalon electrochemical sensors have been previously reported. 41,42 Figure 3D shows the response (the % of the current change) of the two MERS-CoV biosensors towards the binding to the antibody. The results revealed that the responses of the two biosensors were almost similar.…”
Section: Design Of the Cotton-coated Electrochemicalmentioning
confidence: 99%
“…For each device functionalization, DSP solution was added to the chip surface and incubated for 2 h. Then, 10 µL of antibody mixed solution (stock) was added to each device surfaces for 2 h to immobilize one type of antibody to each electrode and then washed with 1 mM PBS for 3 times to remove unbound molecules. Then, the functionalized surfaces were rinsed with 10 mM (pH 8.0) Tris-HCl buffer to neutralized unreacted DSP molecules [36]. Finally, 0.1 µM 6-mercapto-1-hexanol (Sigma Aldrich, Australia) was incubated on the device surfaces for 10 min to block the remaining surfaces.…”
Section: Assay Protocol Signal Detection and Analysismentioning
confidence: 99%
“…This was done based on the findings from a recent study by Zorea et al, where it was found that for non-faradaic EIS, with increasing incubation times the measurable values of interfacial capacitance (constant phase element) and resistance (solution and diffusional resistance) decrease. 35 Calibration dose-response curves for EIS-based PGE2 detection in artificial urine (n = 3) and pooled human urine (n = 3) were reported as percentage changes in impedance modulus at 100 Hz relative to a baseline or zero dose as a function of PGE2 concentration. Calibration dose-response curves for MS-based PGE2 detection in artificial urine (n = 3) and pooled human urine (n = 3) were reported as percentage changes in 1/capacitance 2 at 100 Hz relative to a baseline or zero dose as a function of PGE2 concentration.…”
Section: T H Imentioning
confidence: 99%