A label-free ratiometric immunoassay using bioinspired nanochannels and a smart modified electrode.

Anal Chim Acta

Ministry of Education Key Laboratory of Synthetic and Natural Functional Molecular Chemistry, Shanxi Provincial Key Laboratory of Electroanalytical Chemistry, College of Chemistry & Materials Science, Northwest University, Xi'an 710127, China.

Published: June 2021

Labeling with redox reporter is often required in developing electrochemical bioassay for most proteins or nucleic acid biomarkers. Herein, a label-free ratiometric immunosensing platform is firstly developed by integrating the antibody-conjugated nanochannels with a smart modified electrode. The electrode modifier is the composite of C, tetraoctylammonium bromide (TOA) and Prussian blue (PB). Cyclic voltammograms of the ultimate C-TOA/PB modified electrode exhibited two pairs of peaks at 0.15 V and -0.13 V, ascribing to the redox of PB and C, respectively. With the addition of K[Fe(CN)] in the electrolyte solution, the peaks of PB decreased due to the adsorption of [Fe(CN)] while the peaks of C increased because of the formation of the ternary complex (TC) C-TOA-[Fe(CN)]. As a result, the peak current ratio I/I decreased gradually with the increment of the concentration of [Fe(CN)]. For the nanochannels-based immunosensing platform, the steric hindrance of the bioconjugated nanochannels varied with the loading amount of the target CA125, and thus [Fe(CN)] passing through the channels was quantitatively affected. And the higher CA125 level was, the less [Fe(CN)] concentration was. And thus, the ratio I/I monitored at the C-TOA/PB modified electrode increased with the increase of the concentration of CA125. The ratiometric immunoassay featured a linear calibration range from 1.0 U mL to 100 U mL with a low detection limit of 0.86 U mL. In addition, the ratiometric immunosensing platform demonstrated good specificity and stability as well as acceptable accuracy in overcoming the effect of electrode passivation which was an inherent problem of electroanalysis.

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http://dx.doi.org/10.1016/j.aca.2021.338476DOI Listing

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