Monoclonal antibody-based fluorescence polarisation immunoassay for nifursol in feed

被引:5
作者
Zhang, Shiwei [1 ,4 ,5 ]
Shen, Yudong [2 ,5 ]
Zhong, Anqing [3 ,4 ]
机构
[1] Enlife Serv Co Ltd, Shenzhen, Peoples R China
[2] S China Agr Univ, Inst Food Qual & Safety, Dept Educ Guangdong Prov, Food Qual & Safety Key Lab, Guangzhou, Peoples R China
[3] Enlife Serv Co Ltd, Shenzhen, Peoples R China
[4] Enlife Serv Co Ltd, Shenzhen 518102, Peoples R China
[5] S China Agr Univ, Inst Food Qual & Safety, Dept Educ Guangdong Prov, Food Qual & Safety Key Lab, Guangzhou 510642, Guangdong, Peoples R China
关键词
nifursol; tracer design; FPIA; monoclonal antibody; feed detection; LINKED-IMMUNOSORBENT-ASSAY; ANIMAL FEEDINGSTUFFS; POULTRY MUSCLE; HAPTEN; TISSUE; ELISA; FURAZOLIDONE; METABOLITES; VALIDATION; RESIDUES;
D O I
10.1080/09540100903449961
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Novel tracers were designed and then used to develop a rapid, specific and sensitive fluorescence polarisation immunoassay (FPIA) method to detect nifursol in feed. The 3-((2-(2-hydroxy-3,5-dinitrobenzoyl)hydrazono)methyl)benzoic acid was used for the production of immunogen and 3,5-dinitrosalicylic acid was used for synthesis of fluorescein-labelled tracer. Based on monoclonal antibody and tracer, an optimised FPIA method was established with IC50 of 5.0 ng mL-1, and low cross-reactivity with other nitrofurans (0.05%). FPIA provides a suitable means for screening of a large number of samples. The limits of detection calculated from the analysis of 20 known negative feed samples (pig feed, chicken feed and fish feed) were 0.4-0.8 ng g-1 (mean + 3 SD). Recoveries of nifursol fortified ranged from 85.0 to 95.0%. The coefficients of variation were less than 10%.
引用
收藏
页码:131 / 141
页数:11
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