| Literature DB >> 32861930 |
Panzhu Qin1, Jianguo Xu2, Li Yao2, Qian Wu2, Chao Yan1, Jianfeng Lu3, Bangben Yao4, Guodong Liu5, Wei Chen6.
Abstract
We propose a visual strategy for simultaneous detection of multiple adulterated components in beef by integration of multiple polymerase chain reaction (mPCR) with the lateral flow strip (LFS). The primer sets for adulterated components are uniquely designed with different nucleic acid tags (NAT), enabling the amplicons with specific wobbled sequences at two opposite ends. The wobbled sequences will precisely hybridize with the pre-immobilized capture probes on T lines (T1, T2 and T3) and C line, contributing to the coloration of LFS. Taking advantages of extraordinary amplification efficiency of PCR and simplicity of LFS, common adulterated components including chicken, duck and pork can be easily detected with LOD as low as 0.01% (wt%), which is comparable to that of quantitative real-time polymerase chain reaction (qPCR) but with more simplified operations and reduced costs. The method can be extended to identification of other components by replacing the functional primer set. This method can be a useful candidate for meat quality control at the resource-limited setups.Entities:
Keywords: Chicken; Duck; Gold nanoparticle; Lateral flow strip; Meat adulteration; Multiple determination; Multiple polymerase chain reaction; Pork
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Year: 2020 PMID: 32861930 DOI: 10.1016/j.foodchem.2020.127891
Source DB: PubMed Journal: Food Chem ISSN: 0308-8146 Impact factor: 7.514