A Triple‐Modal Biosensing Strategy for Hepatitis B Virus Based on Mg 2+ ‐Mediated Modulation of CRISPR/Cas12a and Au@Pt Nanoparticles

Abstract Hepatitis B virus (HBV) infection remains a significant global public health issue, and rapid detection of HBV DNA is crucial for disease prevention and control. However, traditional methods for HBV DNA detection are limited by their reliance on precise instruments and single readout, which can hardly meet the requirements of on‐site detection. In this study, the Mg 2+ ‐enhanced trans‐cleavage activity of clustered regularly interspaced short palindromic repeats/associated protein 12a (CRISPR/Cas12a) is reported and coupled with loop‐mediated isothermal amplification (LAMP) and Au@Pt nanoparticles as a signaling reporter for on‐site detection of HBV DNA. This triple‐modal biosensing strategy enables multiple signal readouts including UV–vis spectrum, RGB value, and temperature with high sensitivity and accuracy. The linear detection ranges using UV–vis spectroscopy, RGB color recognition, and photothermal modes are from 50 to 10,000 copies µL −1 , with the limitation of detection of 24.07, 39.65, and 23.33 copies µL −1 , respectively. This biosensing strategy is further employed for the qualitative detection of HBV DNA in 48 serum samples, achieving sensitivities of 100%, 100%, and 95.24% for triple modes. This work offers a promising tool of next‐generation LAMP‐CRISPR/Cas12a for the rapid and portable detection of nucleic acids.