Rapid one-step enzyme immunoassay and lateral flow immunochromatographic assay for colistin in animal feed and food

被引:1
作者
Jiayi Wang [1 ]
Jinyu Zhou [1 ]
Yiqiang Chen [1 ]
Xinpei Zhang [1 ]
Yongpeng Jin [1 ]
Xiaojing Cui [1 ]
Dongting He [1 ]
Wenqing Lai [1 ]
Lidong He [2 ]
机构
[1] Beijing Advanced Innovation Center for Food Nutrition and Human Health, and State Key Laboratory of Animal Nutrition, College of Animal Science and Technology, China Agricultural University
[2] Department of Chemistry and Biochemistry, Florida State University
关键词
Colistin; ELISA; Feed; Food; Gold nanoparticle; Lateral flow immunochromatographic assay; Monoclonal antibody;
D O I
暂无
中图分类号
S816.17 [饲料检验方法]; O652 [分析作业方法与技术]; TS207.3 [食品分析与检验];
学科分类号
070302 ; 081704 ; 083201 ; 090502 ;
摘要
Background: Colistin(polymyxin E) is a kind of peptide antibiotic which has been approved in animal production for the purposes of disease prevention, treatment, and growth promotion. However, the wide use of colistin in animal feed may accelerate the spread of colistin-resistance gene MCR-1 from animal production to human beings,and its residue in animal-origin food may also pose serious health hazards to humans. Thus, it is necessary to develop corresponding analytical methods to monitor the addition of colistin in animal feed and the colistin residue in animal-origin food.Results: A one-step enzyme-linked immunosorbent assay(ELISA) and a lateral flow immunochromatographic assay(LFIA) for colistin were developed based on a newly developed monoclonal antibody. The ELISA showed a 50%inhibition value(IC50) of 9.7 ng/m L with assay time less than 60 min, while the LFIA had a strip reader-based detection limit of 0.87 ng/m L in phosphate buffer with assay time less than 15 min. For reducing the non-specific adsorption of colistin onto sample vial, the components of sample extraction solution were optimized and proved to greatly improve the assay accuracy. The spiked recovery experiment showed that the recoveries of colistin from feed, milk and meat samples were in the range of 77.83% to 113.38% with coefficient of variations less than 13% by ELISA analysis and less than 18% by LFIA analysis, respectively. Furthermore, actual sample analysis indicated that the two immunoassays can produce results consistent with instrumental analysis.Conclusions: The developed assays can be used for rapid qualitative or quantitative detection of colistin in animal feed and food.
引用
收藏
页码:280 / 289
页数:10
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