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An antibody-magnetic nanoparticle conjugate-based selective filtration method for the rapid colorimetric detection of Listeria monocytogenes

机译:一种基于抗体-磁性纳米粒子共轭物的选择性过滤方法,用于比色法快速检测单核细胞增生性李斯特菌

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In the present study, a method for the rapid colorimetric detection of Listeria monocytogenes based on selective filtration was developed by using monoclonal antibody (MAb)-magnetic nanoparticle (MNP) conjugates with a nitrocellulose filter membrane possessing a pore size of 1.2 μm. The conjugates bound and unbound to L monocytogenes after being isolated on a magnet were directly passed through a nitrocellulose filter membrane by vacuum pressure, and the color signals from conjugate-bacteria that remain on the membrane are measured, reflecting the amount of bacteria in a sample. The capture efficiencies of the conjugates were confirmed to be 48% to 89% for 10~3,10~2, and 10~1 cells per mL of L. monocytogenes. After optimization, 1.2 × 10~1 cells of L. monocytogenes were detectable in a pure pathogen solution from the standard curve, and the cut-off value for artificially inoculated vegetables by the method was 1 × 10~2 cells per g. Although weak cross-reactivity to Listeria spp. and Staphylococcus aureus was observed, the method was confirmed to be highly specific to L. monocytogenes. The method can be concluded within 35 min, yielding results in a shorter or similar period to recently reported antibody-immobilized MNP-based methods without additional steps such as dissociation of the target bacteria from MNP-MAb or enrichment. Therefore, the method could be used as a rapid, sensitive, and cost-effective tool for the detection of L. monocytogenes in various vegetables at a minimum detection level of 1 × 10~2 cells per g.
机译:在本研究中,通过使用单克隆抗体(MAb)-磁性纳米颗粒(MNP)结合物和孔径为1.2μm的硝酸纤维素滤膜,开发了一种基于选择性过滤的比色法快速检测李斯特菌的方法。在磁铁上分离后,与L单核细胞增生因子结合和未结合的结合物通过真空压力直接通过硝化纤维素滤膜,并测量残留在膜上的结合物细菌的颜色信号,从而反映出样品中细菌的数量。每毫升单核细胞增生李斯特菌对10〜3、10〜2和10〜1个细胞的结合物的捕获效率被证实为48%至89%。优化后,从标准曲线上可在纯病原体溶液中检测到1.2×10〜1个单核细胞增生李斯特菌,通过该方法人工接种的蔬菜的临界值为每g 1×10〜2个细胞。虽然与李斯特菌属的交叉反应性较弱。并且观察到金黄色葡萄球菌,该方法对单核细胞增生李斯特菌具有高度特异性。该方法可在35分钟内完成,与最近报道的基于抗体的基于MNP的抗体固定方法相比,可在更短或相似的时间内得到结果,而无需其他步骤,例如从MNP-MAb分离靶细菌或富集。因此,该方法可作为检测各种蔬菜中单核细胞增生李斯特氏菌的快速,灵敏且经济高效的工具,最低检测水平为每克1×10〜2个细胞。

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