4.7 Article

Pop-up paper-based and fully integrated microdevice for point-of-care testing of vancomycin-resistant Enterococcus

期刊

SENSORS AND ACTUATORS B-CHEMICAL
卷 345, 期 -, 页码 -

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.snb.2021.130362

关键词

Pop-up paper-based microdevice; Loop-mediated isothermal amplification; pH-dependent colorimetric detection; Vancomycin-resistant Enterococcus; Point-of-care testing

资金

  1. National Research Foundation of Korea (NRF) - Korea government (MSIT) [NRF2020R1A2B5B01001971]
  2. Exchange of experts in science and technology Project of National Research Foundation of Korea (NRF) - Ministry of Science, ICT [2020H1D2A2099511]
  3. National Research Foundation of Korea [2020H1D2A2099511] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

向作者/读者索取更多资源

The study developed a paper-based microdevice for VRE identification, integrating DNA extraction, LAMP amplification, and colorimetric detection. The device achieved highly sensitive detection with a limit of VRE detection of 102 CFU/mL in milk and holds promise for point-of-care applications in medical and food safety settings. The microdevice allows folding on a 3D paper platform for sample mixing and sequential DNA purification and amplification, providing accurate and rapid diagnosis and control of VRE.
This study presents a pop-up greeting card-inspired paper-based microdevice fully integrating DNA extraction, loop-mediated isothermal amplification (LAMP), and pH-dependent colorimetric detection for vancomycin-resistant Enterococcus (VRE) identification. The microdevice has a 3D paper platform that allows folding to mix the sample and reagents for sequential DNA purification and amplification. An FTA card was used for DNA extraction from intact bacteria in several samples, including bacterial cell culture, milk, and sausage. The extraction zone was then folded to transfer purified DNA in the FTA card to the reaction chamber for the LAMP reaction performed at 65 degrees C. After 45 min, a newly synthesized chemosensor was added to the reaction chamber for the colorimetric detection of the LAMP reaction based on pH changes. The color of the FTA card and LAMP solution turned yellow which indicated the absence of target DNA, whereas the colorless FTA card indicated the presence and successful amplification of target DNA. A highly sensitive detection with the limit of VRE detection of 102 CFU/mL in milk was achieved using this microdevice. The portable and integrated microdevice presented in this study holds significant promise for point-of-care applications to accurately and rapidly diagnose and control VRE not only in food but also in healthcare settings.

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