An immunochromatographic assay for rapid and direct detection of 3-amino-5-morpholino-2-oxazolidone (AMOZ) in meat and feed samples

被引:23
作者
Li, Shuqun [1 ]
Song, Juan [2 ]
Yang, Hong [3 ]
Cao, Biyun [1 ]
Chang, Huafang [1 ]
Deng, Anping [1 ]
机构
[1] Soochow Univ, Key Lab Hlth Chem & Mol Diag Suzhou, Coll Chem Chem Engn & Mat Sci, Suzhou 215123, Peoples R China
[2] Chengdu Ctr Food & Drug Control, Chengdu 610045, Peoples R China
[3] Soochow Univ, Coll Pharm Sci, Suzhou 215123, Peoples R China
基金
中国国家自然科学基金;
关键词
nitrofuran; furaltadone; 3-amino-5-methylmorpholino-2-oxazolidinone (AMOZ); immunochromatographic assay (ICA); monoclonal antibody; colloidal gold nanoparticles; meat and feed samples; LINKED-IMMUNOSORBENT-ASSAY; TANDEM MASS-SPECTROMETRY; SOLID-PHASE EXTRACTION; ANTIBODY-BASED ELISA; LIQUID-CHROMATOGRAPHY; MONOCLONAL-ANTIBODY; FURAZOLIDONE METABOLITE; NITROFURAN METABOLITE; BOUND RESIDUES; ANIMAL FEEDS;
D O I
10.1002/jsfa.6423
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
BACKGROUNDFuraltadone (FTD) is a type of nitrofuran and has been banned in many countries as a veterinary drug in food-producing animals owing to its potential carcinogenicity and mutagenicity. FTD is unstable in vivo, rapidly metabolizing to 3-amino-5-methylmorpholino-2-oxazolidinone (AMOZ); thus AMOZ can be used as an indicator for illegal usage of FTD. Usually, for the determination of nitrofurans, the analyte is often a derivative of the metabolite rather than the metabolite itself. In this study, based on the monoclonal antibody (mAb) against AMOZ, a competitive immunochromatographic assay (ICA) using a colloidal gold-mAb probe for rapid and direct detection of AMOZ without a derivatization step in meat and feed samples was developed. RESULTSThe intensity of red color in the test line is inversely related to the analyte concentration and the visual detection limit was found to be 10 ng mL(-1). The performance of this assay was simple and convenient because the tedious and time-consuming derivatization step was avoided. The ICA detection was completed within 10 min. The ICA strips could be used for 7 weeks at room temperature without significant loss of activity. The AMOZ spiked samples were detected by ICA and confirmed by enzyme-linked immunosorbent assay. The results of the two methods were in good agreement. CONCLUSIONThe proposed ICA provides a feasible tool for simple, sensitive, rapid, convenient and semi-quantitative detection of AMOZ in meat and feed samples on site. To our knowledge, this is the first report of the ICA for direct detection of AMOZ. (c) 2013 Society of Chemical Industry
引用
收藏
页码:760 / 767
页数:8
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