A novel split-type photoelectrochemical immunosensor based on chemical redox cycling amplification for sensitive detection of cardiac troponin I

Photoelectrochemical (PEC) immunoassay is a burgeoning and promising bioanalytical method. However, the practical application of PEC still exist some challenges such as the inevitable damage of biomolecules caused by the PEC system and the unsatisfactory sensitivity for biomarkers with low abundance in real sample. To solve the problems, we integrated the cosensitized structure of Ag2S/ZnO nanocomposities as photoelectrode with photogenerated hole-induced chemical redox cycling amplification (CRCA) strategy to develop a split-type PEC immunosensor for cardiac troponin I (cTnI) with high sensitivity. Initially, the immunoreaction was carried out on the 96-well plates in which alkaline phosphatase (ALP) could catalyze ascorbic acid 2-phosphate (AAP) to generate the signal-reporting species ascorbic acid (AA). Subsequently, the AA participated and the tris (2-carboxyethyl) phosphine (TCEP) mediated chemical redox cycling reaction took place on the photoelectrode, thus leading to signal amplification. Under the optimized conditions, the immunosensor demonstrated a detection limit (LOD) of 3.0 x 10(-15) g mL(-1) with a detection range of 1.0 x 10(-14) g mL(-1) to 1.0 x 10(-9) g mL(-1) for cTnI. Impressively, the proposed method could determine the cTnI in human serum samples with high sensitivity and satisfactory accuracy. Considering the virtues of the photoelectrode and the chemical redox cycling strategy, the method would hold great potential for highly sensitive biosensing and bioanalysis.

Automated summary

The split-type PEC immunosensor developed in this study utilizes the cosensitized structure of Ag2S/ZnO nanocomposites as photoelectrode and the photogenerated hole-induced chemical redox cycling amplification strategy, demonstrating high sensitivity for cardiac troponin I (cTnI) detection. By integrating immunoreaction on 96-well plates with chemical redox cycling amplification on the photoelectrode, the immunosensor achieves a detection limit of 3.0 x 10(-15) g mL(-1) and a detection range of 1.0 x 10(-14) g mL(-1) to 1.0 x 10(-9) g mL(-1) for cTnI, showing potential for sensitive biosensing and bioanalysis.