Development and evaluation of immunoassay for zeranol in bovine urine.

被引:16
作者
Liu Y. [1 ]
Zhang C.Z. [1 ]
Yu X.Y. [1 ]
Zhang Z.Y. [1 ]
Zhang X. [1 ]
Liu R.R. [1 ]
Liu X.J. [1 ]
Gong Z.M. [1 ]
机构
[1] Institute of Food Safety, Jiangsu Academy of Agricultural Sciences, Nanjing
来源
Journal of Zhejiang University SCIENCE B | 2007年 / 8卷 / 12期
基金
中国国家自然科学基金;
关键词
Zeranol; Enzyme linked immunosorbent assay (ELISA); Bovine urine; TS201.6;
D O I
10.1631/jzus.2007.B0900
中图分类号
学科分类号
摘要
A high affinity polyclonal antibody-based enzyme linked immunosorbent assay (ELISA) was developed for the quantification of zeranol in bovine urine. On the basis of urine matrix studies, the optimized dilution factors producing insignificant matrix interference were selected as 1:5 in pretreatment. In the improved ELISA, the linear response range was between 0.02 and 1 microg/ml, and the detection limit was 0.02 microg/ml for the assay. The overall recoveries and the coefficients of variation (CVs) were in the range of 82% to approximately 127% and 3.5% to approximately 8.8%, respectively. Thirty-six bovine urine samples spiked with zeranol (ranging from 0.2 to 10 microg/ml) were detected by the ELISA and liquid chromatography (LC) method, and good correlations were obtained between the two methods (R(2)=0.9643). We conclude that this improved ELISA is suitable tool for a mass zeranol screening and can be an alternative for the conventional LC method for zeranol in bovine urine.
引用
收藏
页码:900 / 905
页数:5
相关论文
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