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结合基于智能手机的原始图像分析和液相色谱-质谱联用技术对侧向流动分析中所含蛋白质进行定量,实现食品安全过敏原的准确测定。

Secure Food-Allergen Determination by Combining Smartphone-Based Raw Image Analyses and Liquid Chromatography-Mass Spectrometry for the Quantification of Proteins Contained in Lateral Flow Assays.

机构信息

Agriculture and Food, Commonwealth Scientific and Industrial Research Organisation (CSIRO), St Lucia, Queensland 4067, Australia.

Institute for Global Food Security, Queen's University Belfast, Belfast BT9 5DL, U.K.

出版信息

Anal Chem. 2022 Dec 13;94(49):17046-17054. doi: 10.1021/acs.analchem.2c03000. Epub 2022 Nov 29.

DOI:10.1021/acs.analchem.2c03000
PMID:36445804
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9753063/
Abstract

The current food safety testing system, based on laboratory-based quantification, is difficult to scale up in line with the growth in the export market and does not enable traceability through the nodes of the food supply system. Screening assays, for example, lateral flow assays (LFAs), can improve traceability but often lack the required reliability to guarantee compliance. Here, we present an alternative pipeline for secure on-site compliance testing, using allergens as a case study. The pipeline features smartphone-driven LFA quantification and an liquid chromatography-mass spectrometry (LC-MS) method enabling direct quantification of the allergens contained in the LFA. The system enables swift and objective screening and provides a control measure to verify LFA assay reliability. For the smartphone assay, 8-bit RGB and grayscale colorimetric channels were compared with 16-bit raw intensity values. The latter outperformed RGB and grayscale channels in sensitivity, repeatability, and precision, while ratiometric ambient light correction resulted in excellent robustness for light-intensity variation. Calibration curves for peanut determination using two commercial LFAs featured excellent analytical parameters ( = 0.97-0.99; RSD 7-1%; LOD 3-7 ppm). Gluten determination with a third commercial LFA was equally established. A prediction error of 13 ± 11% was achieved for the best performing assay. Good performance-calibration curves ( = 0.93-0.99) and CVs (<15%)- were observed for the analyte quantification from the LFA by LC-MS. The LOD for the LC-MS assay was 0.5 ppm, well below the LODs reported for the LFAs. This method creates a digital, fast, and secure food safety compliance testing paradigm that can benefit the industry and consumer alike.

摘要

当前的食品安全检测系统基于实验室定量分析,难以与出口市场的增长保持同步,并且无法实现食品供应系统节点的可追溯性。例如,筛选检测,如横向流动分析(LFA),可以提高可追溯性,但通常缺乏保证合规所需的可靠性。在这里,我们提出了一种替代的安全现场合规测试方案,以过敏原为例。该方案具有智能手机驱动的 LFA 定量分析和液相色谱-质谱(LC-MS)方法,能够直接定量 LFA 中包含的过敏原。该系统能够快速进行客观筛选,并提供控制措施来验证 LFA 检测的可靠性。对于智能手机检测,8 位 RGB 和灰度比色通道与 16 位原始强度值进行了比较。后者在灵敏度、重复性和精度方面优于 RGB 和灰度通道,而比率环境光校正对光强变化具有出色的稳健性。使用两种商业 LFA 测定花生的校准曲线具有出色的分析参数( = 0.97-0.99;RSD 7-1%;LOD 3-7 ppm)。使用第三种商业 LFA 同样可以确定面筋。表现最佳的检测方法的预测误差为 13 ± 11%。通过 LC-MS 从 LFA 定量分析物得到了良好的性能-校准曲线( = 0.93-0.99)和 CVs(<15%)。LC-MS 检测方法的 LOD 为 0.5 ppm,远低于 LFA 报道的 LOD。该方法创建了一种数字化、快速和安全的食品安全合规测试范例,可以使行业和消费者受益。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c4c/9753063/c351eeb6fade/ac2c03000_0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c4c/9753063/d8b96a19a279/ac2c03000_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c4c/9753063/8c22c14abd0e/ac2c03000_0003.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c4c/9753063/31702158f952/ac2c03000_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c4c/9753063/c351eeb6fade/ac2c03000_0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c4c/9753063/d8b96a19a279/ac2c03000_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c4c/9753063/8c22c14abd0e/ac2c03000_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c4c/9753063/cce6cd5463f2/ac2c03000_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c4c/9753063/31702158f952/ac2c03000_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c4c/9753063/c351eeb6fade/ac2c03000_0006.jpg

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