NLISA versus enzyme‐linked immunosorbent assay: Nanozyme‐linked immunosorbent array based on platinum sub‐nanocluster nanozyme for α‐fetoprotein detection

Abstract

AbstractRapid and accurate identification of tumor metabolic markers is important for early tumor diagnosis and individualized treatment. Here, a stable monodisperse sub‐nanometer platinum (Pt) material was developed as a highly efficient nanozyme with a specific activity of peroxidase as high as 20.86 U mg−1 through the growth of in situ domain‐limited Pt quantum dots via the polymer polyvinylpyrrolidone. Further, the synthesis of large quantities of Pt‐loaded SiO2 (Pt‐SiO2) was determined by silylation reaction and used for naked eye colorimetric testing of human alpha‐fetoprotein (AFP). In particular, the immunization incubation process occurred in preprepared microplates. A nanozyme‐based immunomodel was constructed in the presence of the target AFP, and a chromogenic reaction occurred with exogenous hydrogen peroxide and the chromogenic substrate tetramethylbenzidine. On optimization of experimental conditions, the dynamic working response range for AFP was found to be 0.05–20 ng mL−1, with a limit of detection of 38.7 pg mL−1. This work provides a new strategy to design efficient nanozyme‐based enzyme‐linked immunochromatographic platforms to meet the practical use of replacing natural enzymes.