4.7 Article

Rapid colorimetric detection of Salmonella typhimuriumusing a selective filtration technique combined with antibody-magnetic nanoparticle nanocomposites

期刊

ANALYTICAL AND BIOANALYTICAL CHEMISTRY
卷 406, 期 3, 页码 859-866

出版社

SPRINGER HEIDELBERG
DOI: 10.1007/s00216-013-7497-6

关键词

Antibody-magnetic nanoparticle; Colorimetric detection; Selective filtration; Salmonella typhimurium

资金

  1. NLRL Program [2001-0028915]
  2. Converging Research Center Program through the National Research Foundation of Korea (NRF) [2013K000242]
  3. Korean Ministry of Science, ICT & Future Planning
  4. Fishery Commercialization Technology Development Program, Korean Ministry of Oceans and Fisheries

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Detection of pathogenic bacteria that pose a great risk to human health requires a rapid, convenient, reliable, and sensitive detection method. In this study, we developed a selective filtration method using monoclonal antibody (MAb)-magnetic nanoparticle (MNP) nanocomposites for the rapid and sensitive colorimetric detection of Salmonella typhimurium. The method contains two key steps: the immunomagnetic separation of the bacteria using MAb-MNP nanocomposites and the filtration of the nanocomposite-bound bacteria. Color signals from the nanocomposites remaining on the membrane were measured, which reflected the amount of bacteria in test samples. Immunomagnetic capture efficiencies of 8 to 90 % for various concentrations of the pathogen (2 x 10(4)-2 x 10(1) cells) were obtained. After optimization of the method, 2 x 10(1) cells of S. typhimurium in pure culture solution was detectable as well as in artificially inoculated vegetables (100 cells/g). The method was confirmed to be highly specific to S. typhimurium without cross-reaction to other pathogenic bacteria and could be concluded within 45 min, yielding results in a shorter or similar time period as compared with recently reported antibody immobilized on magnetic-particle-based methods. This study also demonstrated direct application of MAb-MNP nanocomposites without a dissociation step of bacteria from magnetic beads in colorimetric assays in practice.

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