A new strategy for label-free electrochemical immunoassay based on “gate-effect” of β-cyclodextrin modified electrode
A novel label-free electrochemical immunoassay was developed for prostate-specific antigen (PSA) detection via using β-cyclodextrin (β-CD) assembled layer created gates for the electron transfer of probe. To construct the sensor, a gold electrode was self-assembled with monoclonal anti-PSA antibody...
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Veröffentlicht in: | Analytica chimica acta 2016-07, Vol.926, p.48-54 |
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Sprache: | eng |
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Zusammenfassung: | A novel label-free electrochemical immunoassay was developed for prostate-specific antigen (PSA) detection via using β-cyclodextrin (β-CD) assembled layer created gates for the electron transfer of probe. To construct the sensor, a gold electrode was self-assembled with monoclonal anti-PSA antibody labeled 6-mercapto-β-cyclodextrin. Interspaces among β-CD molecules in the layer were automatically formed on gold electrode, which act as the channel of the electron transfer of [Fe(CN)6]3−/4− probe. When PSA bind with anti-PSA, it can block these channels on the electrode surface due to their steric hindrance effect, resulting in the decrease in redox current of the probe. Through such a gate-controlled effect, ultra trace amount of PSA may make the currents change greatly after the immunoreaction, which enhanced the signal-to-noise ratio to achieve the amplification effect. By evaluating the logarithm of PSA concentrations, the immunosensor had a good linear response to the current changes with a detection limit of 0.3 pg/mL (S/N = 3) when PSA concentration ranged from 1.0 pg/mL to 1.0 ng/mL. The label-free immunosensor exhibited satisfactory performances in sensitivity, repeatability as well as specificity.
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•A label-free PSA immunoassay was developed based on “gate-effect” amplification.•Interspaces among β-CD assembled for [Fe(CN)6]3−/4− electron transfer were controlled by the immunoreaction.•Higher sensitivity was achieved with time and cost saving principle. |
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ISSN: | 0003-2670 1873-4324 |
DOI: | 10.1016/j.aca.2016.04.035 |