Matrix redox interference-free nanozyme-amplified detection of Hg2+using thiol-modified phosphatase-mimetic nanoceria

Given heavy metals pose huge threats to ecological system and human health, it is significant to monitor them. With the favorable feature of catalytic signal amplification, redox-type nanozymes have been widely used to detect heavy metals. However, the presence of redox substances in samples can interfere with these catalytic reactions, impacting the accuracy and repeatability of detection. To avoid the situation, here we designed a nonredox nanozyme (3-mercaptopropionic acid modified nanoceria, MPA-CeO2) and developed a novel approach free from matrix redox interference to detect Hg2+. The well-dispersed MPA-CeO2 showed high and stable phosphatase-mimetic activity to catalyze the hydrolysis of colorless p-nitrophenyl phosphate (p-NPP) to yellow pnitrophenol (p-NP). The addition of Hg2+ could bind specifically onto the MPA-CeO2 particles through S-Hg bond and cause the latter to aggregate, thereby suppressing the ability of MPA-CeO2 with shielded active surfaces to hydrolyze p-NPP. According to the simple principle, highly sensitive and specific colorimetric measurement of Hg2+ was achieved, and excellent reliability and practicability were demonstrated by real sample analysis. To our best knowledge, this study is the first one of detecting Hg2+ using phosphatase-mimicking nanozymes, and it will inspire the exploration of new analytical methods via designing non-redox nanozymes for various targets.

Automated summary

Given the significant threats of heavy metals to ecological systems and human health, monitoring them is crucial. This study designs a non-redox nanozyme for detecting Hg2+ without interference from redox substances. The approach demonstrates highly sensitive and specific measurement of Hg2+ with excellent reliability and practicability. It is the first study to detect Hg2+ using phosphatase-mimicking nanozymes, inspiring exploration of new analytical methods with non-redox nanozymes.