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作 者:Yanqi Wu Yuhong Guan Peilin Huang Hui Chen Liping Bai Zhihong Jiang
机构地区:[1]State Key Laboratory of Quality Research in Chinese Medicine,Macao University of Science and Technology,Macao 999078,China [2]Shenzhen LemnisCare Medical Technology Co.,Ltd.,Shenzhen 518107,China [3]Hunan Key Laboratory of Biomedical Nanomaterials and Devices,Hunan University of Technology,Zhuzhou 412077,China
出 处:《Chinese Chemical Letters》2024年第9期262-265,共4页中国化学快报(英文版)
基 金:funded by the Science and Technology Development Fund,Macao SAR(Nos.0065/2020/A2,SKLQRCM(MUST)-2020-2022);Shenzhen-Hong Kong-Macao Science and Technology Project(Grade c)(No.SGDX20210823104201010).
摘 要:Norovirus is an infectious disease that can cause non-bacterial gastroenteritis,which has a low infectious dose,rapid onset,and strong transmission ability;therefore,rapid and sensitive detection is essential to reduce the transmission of gastroenteritis.In the study,a norovirus GII loop-mediated isothermal amplification assay was developed and prepared into freeze-drying microspheres,and a closed-cassette-based,integrated,reagent-ambient storage,on-site instant detection platform for norovirus GII was constructed using a commercial,fully automated nucleic acid analyzer with integrated magnetic bearing based nuclear acid extraction and nucleic acid detection,with a sensitivity of 10 copies/μL,with no cross-reactivity with other 5 viruses.For 28 simulated samples,the integrated assay platform was consistent with the experimental results of reverse transcription-quantitative polymerase chain reaction(RT-qPCR)assays after conventional laboratory nucleic acid extraction.The entire process can be finished in about 1 h,which is ideal for immediate rapid detection.
关 键 词:Freeze-dried microspheres Point-of-care testing Loop-mediated isothermal amplification Norovirus GII Integrated testing
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