Development and validation of a rapid test system for detection of pork meat and collagen residues

被引:29
作者
Masiri, J. [1 ]
Benoit, L. [2 ]
Barrios-Lopez, B. [1 ]
Thienes, C. [1 ]
Meshgi, M. [1 ]
Agapov, A. [1 ]
Dobritsa, A. [1 ]
Nadala, C. [1 ]
Samadpour, M. [1 ,2 ]
机构
[1] Mol Epidemiol Inc MEI, 15300 Bothell Way NE, Lake Forest Pk, WA 98155 USA
[2] IEH Labs & Consulting Grp IEH, 15300 Bothell Way NE, Lake Forest Pk, WA 98155 USA
关键词
Adulteration; Lateral flow device (LFD); Polyclonal antibodies; Pork; Gelatin; Meat; SPECIES IDENTIFICATION; MASS-SPECTROMETRY; PCR ASSAY; PRODUCTS; AUTHENTICATION; PORCINE; FRAUD; CHAIN; BEEF; RAW;
D O I
10.1016/j.meatsci.2016.07.006
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Mislabeling, contamination, and economic adulteration of meat products with undeclared pork tissues are illegal under regulations promulgated by numerous regulatory agencies. Nonetheless, analysis of the European meat industry has revealed pervasive meat adulteration, necessitating more extensive application of meat authentication testing. As existing methods for meat speciation require specialized equipment and/or training, we developed a detection system based on a lateral flow device (LFD) assay format capable of rapidly (similar to 35 min) identifying porcine residues derived from raw meat, cooked meat, and gelatin down to 0.01%, 1.0%, and 2.5% contamination, respectively. Specificity analysis revealed no cross-reactivity with meat derived from chicken, turkey, horse, beef, lamb, or goat. Comparison with a commercial ELISA kit and PCR method revealed similar if not improved sensitivity, with the added feature that the LFD-based system required considerably less time to perform. Accordingly, this test system should aid the food industry and food control authorities in monitoring for adulteration with pork. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:397 / 402
页数:6
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