A sensitive and quantitative fluorescent multi-component immuno-chromatographic sensor for β-agonist residues

被引:60
|
作者
Wang, Peilong [1 ,2 ]
Wang, Zhi [3 ]
Su, Xiaoou [1 ,2 ]
机构
[1] Minist Agr, Key Lab Agroprod Safety & Qual, Beijing 100081, Peoples R China
[2] Chinese Acad Agr Sci, Inst Qual Stand & Testing Technol Agroprod, Beijing 100081, Peoples R China
[3] Beijing Zhifeng Botai Biotechnol Co Ltd, Beijing 102200, Peoples R China
来源
基金
中国国家自然科学基金;
关键词
beta-Agonist; Fluorescent bead; Immuno-chromatographic sensor; Multi-analyte detection; PERFORMANCE LIQUID-CHROMATOGRAPHY; FLOW TEST STRIP; ELECTROCHEMICAL DETECTION; MULTIRESIDUE ANALYSIS; MASS-SPECTROMETRY; CLENBUTEROL; URINE; LIVER; EXTRACTION; BOVINE;
D O I
10.1016/j.bios.2014.09.064
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
A sensitive and quantitative fluorescent multi-component immuno-chromatographic sensor was developed for detection of three beta-agonizts: clenbuterol, ractopamine and salbuterol. A competitive immune strategy between antibody conjugated fluorescent beads and beta-agonist or their antigens was employed. Each monoclonal antibody specifically recognizes it is corresponding beta-agonist in the conjugating zone. The unreacted antibodies were captured by beta-agonist antigens immobilized at three test lines in nitrocellulose membrane reaction zone. This enables simultaneous detection of 3 beta-agonizts in one single test without any further sample preparation. The test results can be obtained within 10 min. Limit of detections for clenbuterol, ractopamine and salbuterol were 0.10 ng/mL, 0.10 ng/mL and 0.09 ng/mL, respectively. Recoveries ranged from 70.0% to 100.5% and relative standard deviations were below 15%. The assay was evaluated using spiked and real samples and the results were compared with LC-MS/MS. The developed novel assay method provides a low cost, sensitive and rapid approach for on site detection of beta-agonizts. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:511 / 516
页数:6
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