| Literature DB >> 26776037 |
Fang Cheng1, Jiajie Wu1, Jin Zhang2, Aihu Pan1, Sheng Quan1, Dabing Zhang3, HaeYeong Kim4, Xiang Li5, Shan Zhou2, Litao Yang6.
Abstract
Food allergies cause health risks to susceptible consumers and regulations on labeling of food allergen contents have been implemented in many countries and regions. To achieve timely and accurate food allergen labeling, the development of fast and effective allergen detection methods is very important. Herein, a decaplex polymerase chain reaction (PCR) assay combined with capillary electrophoresis was developed to detect simultaneously 10 common food allergens from hazelnut, pistachio, oat, sesame, peanut, cashew, barley, wheat, soybean and pecan. The absolute limit of detection (LODa) of this system is between 2 and 20 copies of haploid genome, and the relative LOD (LODr) is as low as 0.005% (w/w) in simulated food mixtures. The developed assay was subsequently applied to 20 commercial food products and verified the allergen ingredients stated on the labels. Furthermore, results using this decaplex PCR assay was successfully replicated in three other laboratories, demonstrating the repeatability and applicability of this assay in routine analysis of the 10 food allergens.Entities:
Keywords: Capillary electrophoresis; Decaplex polymerase chain reaction; Food allergen; Inter-laboratory transfer
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Year: 2015 PMID: 26776037 DOI: 10.1016/j.foodchem.2015.12.058
Source DB: PubMed Journal: Food Chem ISSN: 0308-8146 Impact factor: 7.514