在微阵列芯片PCR导向的微流控横向流动条带装置上精确分子识别不同的肉类掺假而不携带污染物

IF 4.1 Q2 FOOD SCIENCE & TECHNOLOGY Food Chemistry Molecular Sciences Pub Date : 2023-08-12 DOI:10.1016/j.fochms.2023.100180
Hanling Wang , Xianzhuo Meng , Li Yao , Qian Wu , Bangben Yao , Zhaoran Chen , Jianguo Xu , Wei Chen
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引用次数: 1

摘要

基于肉类掺假的食品欺诈最近已成为全球主要的经济、非法、宗教和公共卫生问题之一。在这项工作中,我们开发了一种微阵列芯片聚合酶链式反应(PCR)导向的微流体横向流动条带(LFS)设备,该设备有助于准确和同时识别掺有鸡肉、鸭肉和猪肉的牛肉,特别是在加工牛肉产品中。为了实现这一目标,设计并应用四对扩增引物在微阵列芯片中特异性扩增从混合肉粉中提取的基因组DNA。该装置的突出优点在于样品加载、检测和报告在微观结构中的灵活组合和集成,所有DNA扩增子都可以在LFS单元上单独可视化,导致出现了用于牛肉产品中物种鉴定和定量的测试线(TC线、TD线、TP线或TB线)以及对照线(C线)。基于这种新方法,在低至0.01%(wt.%)的混合物中成功地区分和鉴定了掺杂物,同时有效地避免了常规分子诊断实验室中携带的气凝胶污染。通过使用实时PCR作为金标准对照,成功鉴定了来自当地市场的50个加工绞肉样本,进一步证实了该装置的实用性、准确性和可靠性。本文提出的方法和装置可以是用于食品认证的现场识别的有用工具。
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Accurate molecular identification of different meat adulterations without carryover contaminations on a microarray chip PCR-directed microfluidic lateral flow strip device

Meat adulteration-based food fraud has recently become one of the global major economical, illegal, religious, and public health concerns. In this work, we developed a microarray chip polymerase chain reaction (PCR)-directed microfluidic lateral flow strip (LFS) device that facilitates the accurate and simultaneous identification of beef adulterated with chicken, duck, and pork, especially in processed beef products. To realize this goal, four pairs of amplification primers were designed and applied for specifically amplifying genomic DNA extracted from mixed meat powders in microarray chip. With the prominent advantage of this device lies in the flexible combination and integration of sample loading, detection, and reporting in microstructures, all the DNA amplicons can be individually visualized on the LFS unit, leading to the appearance of test lines (TC line, TD line, TP line, or TB line) as well as the control line (C line) for the species identification and quantification in beef products. Based on this new method, the adulterants were successfully distinguished and identified in mixtures down to 0.01% (wt.%) while the carryover aerogel contamination in routine molecular diagnostic laboratories was effectively avoided. The practicability, accuracy, and reliability of the device were further confirmed by using real-time PCR as a gold standard control on the successful identification of 50 processed ground meat samples sourced from local markets. The method and device proposed herein could be a useful tool for on-site identification of food authentication.

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来源期刊
Food Chemistry Molecular Sciences
Food Chemistry Molecular Sciences Agricultural and Biological Sciences-Food Science
CiteScore
6.00
自引率
0.00%
发文量
83
审稿时长
82 days
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