摘要
Electrochemical sensors that incorporate immunoassay principles have the ability to monitor dynamic processes of antigen–antibody interactions in real time. In this study, a gold electrode was modified with tin dioxide colloidal quantum wire (SnO 2 QWs) and then coated with the leucine/arginine subtype microcystin (MC-LR) antibody. The active site of SnO 2 QWs that was not bound by MC-LR antibody was then passivated with bovine serum protein (BSA). When the MC-LR antigen binds specifically to the antibodies on the electrode's surface, it triggers electrochemical reactions and generates electrical signals at specific voltage conditions. The SnO 2 QW exhibits excellent electron transport ability, and its ability to form a loose and porous microstructure on the gold electrode surface, which is conducive to the receptor function of the biosensor. The results show a high affinity between the MC-LR antigen and antibody, ranging from 1 pg/mL to 10 ng/mL of MC-LR antigen concentration. The kinetic characteristics of the immune reaction between MC-LR antigen and antibody were elucidated, obtaining a binding constant of 1.399 × 10 11 M −1 and a dissociation constant of 7.147 pM, demonstrating the potential of electrochemical biosensing technology in biomolecular interactions.
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