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Updated: May 8, 2026

Foodborne Pathogen Screening Using Magneto-fluorescent Nanosensor: Rapid Detection of E. Coli O157:H7
Published on: September 17, 2017
Magnetically induced aggregation-assisted mesoporous polydopamine/single-atom nanozyme platform for dual-channel
Lulu Cao1, Yuwei Wu2, Yuwei Ren3
1State Key Laboratory of Applied Microbiology Southern China, Guangdong Provincial Key Laboratory of Microbial Safety and Health, National Health Commission Science and Technology Innovation Platform for Nutrition and Safety of Microbial Food, Key Laboratory of Big Data Technologies for Food Microbiological Safety, State Administration for Market Regulation, Institute of Microbiology, Guangdong Academy of Sciences, Guangzhou, 510070, China; Food and Drug Laboratory, Guangdong Detection Center of Microbiology, Guangzhou, 510070, China; School of Food and Biological Engineering, Hefei University of Technology, Hefei, 230009, China.
Abstract:
Contamination with foodborne pathogenic bacteria poses a severe threat to public health, necessitating the integration of detection with source sterilization technologies. Herein, we developed an integrated nanoplatform by combining an aptamer-modified mesoporous polydopamine/palladium single-atom carbon dot composite probe (MPDA/Pd SA@DA-CDs/Apt) with an efficient magnetic separation module (MNRs/PGA/AM). This platform enables colorimetric-photothermal dual-modal detection and two-stage propulsion synergistic sterilization, allowing for precise monitoring and on-site elimination of Escherichia coli O157:H7. The dual-modal detection is realized by MPDA/Pd SA@DA-CDs/Apt: the peroxidase-like activity of Pd SA@DA-CDs catalyzes the 3,3',5,5'-tetramethylbenzidine (TMB)-H2O2 system to generate a colorimetric signal, while the photothermal effect of MPDA outputs a temperature signal under 808 nm laser irradiation. Concurrently, the magnetic module MNRs/PGA/AM significantly enhances the enrichment efficiency of target bacteria and eliminates matrix interference. Dual-modal detection exhibits excellent linearity within the range of 102-108 cfu/mL, with detection limits of 8.6 × 101 cfu/mL (colorimetry) and 4.6 × 101 cfu/mL (photothermal). Signal cross-verification minimizes false results. Upon positive detection, a two-stage synergistic sterilization strategy is initiated: first, the spatial aggregation effect induced by the magnetic module significantly shortens the interaction distance; simultaneously, the targeted MPDA/Pd SA@DA-CDs/Apt probe adsorbs onto bacterial surfaces, where the photothermal effect of MPDA under near-infrared irradiation accelerates reactive oxygen species generation from the Pd SA@DA-CDs catalyst, thereby promoting a secondary sterilization boost. This synergistic mechanism achieves a 100% kill rate against planktonic bacteria and effectively disrupts biofilms. This study provides an innovative "detection-sterilization" integrated solution for controlling foodborne pathogens, significantly reducing the risks of cross-contamination and antibiotic resistance.
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