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A Critical Comparison between Flow-through and Lateral Flow Immunoassay Formats for Visual and Smartphone-Based Multiplex Allergen Detection

机译:视觉和基于智能手机的多重过敏原检测的流过和横向流免疫分析形式之间的关键比较

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摘要

(1) Background: The lack of globally standardized allergen labeling legislation necessitates consumer-focused multiplexed testing devices. These should be easy to operate, fast, sensitive and robust. (2) Methods: Herein, we describe the development of three different formats for multiplexed food allergen detection, namely active and passive flow-through assays, and lateral flow immunoassays with different test line configurations. (3) Results: The fastest assay time was 1 min, whereas even the slowest assay was within 10 min. With the passive flow approach, the limits of detection (LOD) of 0.1 and 0.5 ppm for total hazelnut protein (THP) and total peanut protein (TPP) in spiked buffer were reached, or 1 and 5 ppm of THP and TPP spiked into matrix. In comparison, the active flow approach reached LODs of 0.05 ppm for both analytes in buffer and 0.5 and 1 ppm of THP and TPP spiked into matrix. The optimized LFIA configuration reached LODs of 0.1 and 0.5 ppm of THP and TPP spiked into buffer or 0.5 ppm for both analytes spiked into matrix. The optimized LFIA was validated by testing in 20 different blank and spiked matrices. Using device-independent color space for smartphone analysis, two different smartphone models were used for the analysis of optimized assays.
机译:(1)背景:缺乏全球标准化的过敏原标签立法,因此需要以消费者为中心的多重测试设备。这些应易于操作,快速,灵敏且坚固。 (2)方法:在此,我们描述了三种用于多种食品过敏原检测的格式的发展,即主动和被动流通式检测以及具有不同测试线配置的侧向流免疫检测。 (3)结果:最快的分析时间为1分钟,而最慢的分析时间为10分钟。采用被动流动方法时,加标缓冲液中的总榛子蛋白(THP)和总花生蛋白(TPP)的检出限(LOD)分别为0.1和0.5 ppm,或者将1和5 ppm的THP和TPP加标到基质中。相比之下,对于缓冲液中的两种分析物以及加到基质中的THP和TPP分别为0.5和1 ppm,主动流动方法的LOD达到0.05 ppm。优化的LFIA配置达到了加到缓冲液中的THP和TPP的LOD为0.1和0.5 ppm或加到基质中的两种分析物的LOD为0.5 ppm。通过在20种不同的空白和加标基质中进行测试,验证了优化的LFIA。使用与设备无关的色彩空间进行智能手机分析,使用了两种不同的智能手机模型来分析优化的检测方法。

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