Why the study?
Reported electrochemical conditions for aptasensors varied across studies, prompting optimization of conditions using Fe(CN)63−/4− as a redox marker to improve sensitivity for norovirus aptasensors.
Optimized electrochemical conditions using a screen-printed gold electrode and specific electrolyte concentrations improved the sensitivity of an aptasensor for detecting murine norovirus.
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Hypothesis-generating for electrochemical viral aptasensors; leaves open human diagnostic translation.
Electrochemical biosensors have attracted significant attention as a novel tool for the sensitive detection of pathogens and contaminants, with the potential capability of rapid, on-site diagnosis. In this study, we intended to improve the sensitivity of electrochemical biosensor using Fe(CN)63−/4− as redox marker, toward its application to norovirus aptasensors. Although many researchers have developed electrochemical aptasensors for various analytes using redox markers, the reported electrochemical conditions under which an aptasensor was examined varied across multiple studies. Here, we performed square-wave voltammetry (SWV) for electrodes modified with aptamer specific to murine norovirus and compared the reduction peak currents of Fe(CN)63− under various conditions. Effects of working electrode materials and NaCl and [Ru(NH3)6]Cl3 concentration in the electrolyte were examined. Among conditions we tested, the best sensitivity was obtained using a screen-printed gold electrode in an electrolyte containing 1 M NaCl with 4 mM K3[Fe(CN)6], in which the concentration of murine norovirus showed linearity with SWV peak current. This study provided useful information on the electrochemical measurement conditions regarding the development of electrochemical aptasensors.
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Hirano et al. (2020) studied this question.
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