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首页> 外文期刊>International Journal of Food Microbiology >Rapid pathogen detection by lateral-flow immunochromatographic assay with gold nanoparticle-assisted enzyme signal amplification
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Rapid pathogen detection by lateral-flow immunochromatographic assay with gold nanoparticle-assisted enzyme signal amplification

机译:侧向免疫色谱法结合金纳米颗粒辅助酶信号放大技术快速检测病原体

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摘要

To date most LF-ICA format for pathogen detection is based on generating color signals from gold nanoparticle (AuNP) tracers that are perceivable by naked eye but often these methods exhibit sensitivity lower than those associated with the conventional enzyme-based immunological methods or mandated by the regulatory guidelines. By developing AuNP avidin-biotin constructs in which a number of enzymes can be labeled we report on an enhanced LF-ICA system to detect pathogens at very low levels. With this approach we show that as low as 100 CFU/mL of Escherichia coli O157:H7 can be detected, indicating that the limit of detection can be increased by about 1000-fold due to our signal amplification approach. In addition, extensive cross-reactivity experiments were conducted (19 different organisms were used) to test and successfully validate the specificity of the assay. Semi-quantitative analysis can be performed using signal intensities which were correlated with the target pathogen concentrations for calibration by image processing. (C) 2015 Elsevier B.V. All rights reserved.
机译:迄今为止,大多数用于病原体检测的LF-ICA格式都是基于从金纳米粒子(AuNP)示踪剂产生的彩色信号,这些信号可以通过肉眼观察到,但是这些方法的灵敏度通常低于传统的基于酶的免疫学方法或要求的灵敏度。监管准则。通过开发其中可以标记许多酶的AuNP抗生物素蛋白-生物素构建体,我们报道了增强的LF-ICA系统,可检测极低水平的病原体。通过这种方法,我们显示可以检测到低至100 CFU / mL的大肠杆菌O157:H7,这表明由于我们的信号放大方法,检测限可以提高约1000倍。此外,进行了广泛的交叉反应性实验(使用了19种不同的生物)以测试并成功验证测定的特异性。可以使用与目标病原体浓度相关的信号强度进行半定量分析,以通过图像处理进行校准。 (C)2015 Elsevier B.V.保留所有权利。

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