单核细胞增生李斯特菌
荧光
检出限
乳液聚合
李斯特菌
聚合
化学
分子印迹
色谱法
生物化学
生物
细菌
聚合物
有机化学
催化作用
选择性
物理
遗传学
量子力学
作者
Taotao Ren,Yiwei Lu,Peng Liu,Xuelian Hu,Wenxiu Wang,Shuo Wang,Xiuying Liu,Yiwei Tang
标识
DOI:10.1016/j.fochx.2024.101618
摘要
Listeria monocytogenes (L. monocytogenes) is a foodborne pathogen with high morbidity and mortality rates, necessitating rapid detection methods. Current techniques, while reliable, are labor-intensive and not amenable to on-site testing. We report the design and synthesis of a novel imprinted upconversion fluorescence probe through Pickering emulsion polymerization for the specific detection of L. monocytogenes. The probe employs trimethylolpropane trimethacrylate and divinylbenzene as cross-linkers, acryloyl-modified chitosan as a functional monomer, and the bacterium itself as the template. The developed probe demonstrated high specificity and sensitivity in detecting L. monocytogenes, with a limit of detection of 72 CFU/mL. It effectively identified the pathogen in contaminated salmon and chicken samples, with minimal background interference. The integration of molecular imprinting and upconversion fluorescence materials presents a potent and reliable approach for the rapid and specific detection of L. monocytogenes, offering considerable potential for on-site food safety testing.
科研通智能强力驱动
Strongly Powered by AbleSci AI