A novel nanozyme facilitates high-sensitivity detection of hepatic markers ALT and AST, suggesting enhanced reliability for clinical diagnoses.
Probing the activities of alanine aminotransferase (ALT) and aspartate aminotransferase (AST) is of significance for clinical diagnosis of hepatic diseases and monitoring of therapeutic effects. Traditional detection methods often rely on a single signal driven by cascade catalysis of multiple natural enzymes, exposing weaknesses, including poor robustness and limited reliability. To overcome the deficiencies, here we design a novel nanoprobe (Na₂V₆O₁₆/Cu-MOF) with both peroxidase-like catalytic and luminescent properties and establish a colorimetric/fluorescence bimodal method for the on-demand sensing of hepatic ALT and AST. In the bifunctional nanozyme, Na₂V₆O₁₆ exhibits reposeful enzyme-like activity to trigger the oxidation chromogenic process of 3,3',5,5'-tetramethylbenzidine (TMB) via H₂O₂-dependent free radical formation, and the 2-aminoterephthalic acid-coordinated Cu-MOF presents stable luminescence, which can be quenched by blue oxTMB from nanozyme catalysis via the inner filter effect. The presence of ALT or AST mediates the generation of H₂O₂, which consequently modulates the colorimetric turn-on and fluorescence readouts. With the enzyme-nanozyme cascade catalysis facilitated by Na₂V₆O₁₆/Cu-MOF as well as its fluorescent feature, high-sensitivity bimodal detection of ALT and AST was obtained. Importantly, the established system offers robust catalytic performance, and the on-demand readouts enable mutual verification of different responses, both of which jointly improve the dependability of target analysis. Our work provides a reliable strategy for transaminase biomarker detection, contributing new insights into the design of multifunctional nanozymes and their applications in constructing advanced catalytic sensing platforms.
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Wang et al. (2026) studied this question.
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