Boosting the electrochemiluminescence of luminol by high-intensity focused ultrasound pretreatment combined with 1T/2H MoS(2) catalysis to construct a sensitive sensing platform

In the luminol-O(2) ECL system, O(2) as an endogenous coreactant has the advantages of non-toxicity and stability. Improving the efficiency to generate radicals of O(2) is a challenge currently. In this work, a strategy combining physical method - ultrasound and nanomaterial with unique physicochemical properties was designed to enhance the ECL signal of luminol-O(2) system. Specifically, high-intensity focused ultrasound (HIFU) pretreatment as a non-invasive method could generate ROS (H(2)O(2), O(2)(•−), OH•, (1)O(2)) in situ, triggering and boosting the ECL signal of luminol. In addition, 1T/2H MoS(2) with excellent catalytic activity could catalyze the H(2)O(2) produced in situ, accelerate the oxidation of luminol and further enhance the ECL response. At the same time, combined with the catalytic hairpin assembly (CHA) reaction, the constructed ECL biosensing platform showed excellent performance for the detection of miRNA-155. The concentration range of 0.1 fM ∼ 1 nM with the detection limit as low as 0.057 fM were obtained. Furthermore, the ECL biosensor was also successfully applied to the determination of miRNA-155 in human serum samples. The established ECL sensing platform opens up a promising method for the detection of clinical biomarkers.