Development of a Sensitive Monoclonal Antibody-Based Indirect Competitive Enzyme-Linked Immunosorbent Assay for the Determination of Monensin in Edible Chicken Tissues

被引:9
作者
Li, Langhong [1 ,2 ]
Pan, Yuanhu [1 ,2 ]
Tao, Yanfei [1 ,2 ]
Chen, Donmei [1 ,2 ]
Wang, Yulian [1 ,2 ]
Wang, Xu [1 ,2 ]
Liu, Zhenli [1 ,2 ]
Peng, Dapeng [1 ,2 ]
Yuan, Zonghui [1 ,2 ]
机构
[1] Huazhong Agr Univ, Natl Reference Lab Vet Drug Residues HZAU, Wuhan 430070, Hubei, Peoples R China
[2] Huazhong Agr Univ, MOA Key Lab Detect Vet Drug Residues, Wuhan 430070, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
Monensin; Monoclonal antibody; Indirect competitive enzyme-linked immunosorbent assay; Edible chicken tissues; RESIDUES; COCCIDIOSTATS; CHROMATOGRAPHY; VALIDATION; ELISA; EGGS; FOOD;
D O I
10.1007/s12161-019-01461-3
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
To monitor monensin (MON) residues in chicken tissues, a monoclonal antibody (mAb)-based indirect competitive enzyme-linked immunosorbent assay (ic-ELISA) was developed in this study. The haptenMON was obtained by adding hydrochloric acid to a MON salt, and then was coupled with carrier protein. After the inoculation of female Balb/c mice and cell fusions, one cell line, MON/4C9, was obtained. The MON/4C9 antibody exhibited the ability to specifically recognize MON with IC50 1.28 mu g L-1.Based on this mAb, an optimized ic-ELISA protocol was performed using only methanol-water (8:2, v/v) in chicken tissue samples. The limits of detection and the limits of quantification of MON in various sample matrices varied from 0.38 to 1.01 mu g kg(-1). The recoveries ranged from 71.9 to 116.9% in chicken tissues, and the intra- and inter-assay CVs were all less than 18%. Moreover, the developed method also exhibited a positive correlation with the results of HPLC-MS conducted on the samples. These results suggest that the prepared mAb and the developed ic-ELISA method will be a useful tool for detecting MON in chicken tissues.
引用
收藏
页码:1479 / 1486
页数:8
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