Improvement of the stability of immunochromatographic assay for the quantitative detection of clenbuterol in swine urine

被引:0
|
作者
Peng, Tao [1 ]
Yang, Wan-chun [2 ]
Lai, Wei-Hua [1 ]
Xiong, Yong-Hua [1 ]
Wei, Hua [1 ]
Zhang, Jinsheng [1 ]
机构
[1] Nanchang Univ, State Key Lab Food Sci & Technol, Nanchang 330047, Peoples R China
[2] Jiangxi Zodolabs Bioengn Co Ltd, Nanchang 330047, Peoples R China
基金
中国国家自然科学基金;
关键词
SOLID-PHASE EXTRACTION; LATERAL-FLOW ASSAY; MASS-SPECTROMETRY; RAPID DETECTION; TEST STRIP; SAMPLES; ELISA; BETA(2)-AGONISTS;
D O I
10.1039/c4ay01173b
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Clenbuterol is banned as a feed additive in China and in other countries. Lateral-flow immunochromatographic assay can be applied in the quantitative detection of clenbuterol. Our group has previously developed an immunochromatographic assay to detect clenbuterol in swine urine rapidly and quantitatively. This method was based on the ratio of the color intensity of a test line to that of a control line (T/C) to offset the matrix effects of samples and diminish variations among different strips. In this study, the stability of this method was successfully improved and verified by an accelerated aging test that involved storage at 60 degrees C for three weeks. Results showed that the control line was the main factor affecting the strip stability. To improve the stability of the test strip, we mixed the goat anti-mouse antibody spotted on the control line with WellChampion, Antibody Enhancer, and Protein StabilPLUS. Alterations in the T/C ratio were evaluated using negative and positive swine urine samples. Stability was effectively improved by adding WellChampion. Furthermore, the newly prepared strips showed satisfactory stability by drying the nitrocellulose membrane at 60 degrees C for one day.
引用
收藏
页码:7394 / 7398
页数:5
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