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Rapid one-step enzyme immunoassay and lateral flow immunochromatographic assay for colistin in animal feed and food

Rapid one-step enzyme immunoassay and lateral flow immunochromatographic assay for colistin in animal feed and food

作     者:Jiayi Wang Jinyu Zhou Yiqiang Chen Xinpei Zhang Yongpeng Jin Xiaojing Cui Dongting He Wenqing Lai Lidong He Jiayi Wang;Jinyu Zhou;Yiqiang Chen;Xinpei Zhang;Yongpeng Jin;Xiaojing Cui;Dongting He;Wenqing Lai;Lidong He

作者机构:Beijing Advanced Innovation Center for Food Nutrition and Human Healthand State Key Laboratory of Animal NutritionCollege of Animal Science and TechnologyChina Agricultural UniversityBeijingChina Department of Chemistry and BiochemistryFlorida State UniversityTallahasseeFLUSA. 

出 版 物:《Journal of Animal Science and Biotechnology》 (畜牧与生物技术杂志(英文版))

年 卷 期:2020年第11卷第1期

页      面:280-289页

核心收录:

学科分类:090502[农学-动物营养与饲料科学] 081704[工学-应用化学] 07[理学] 0905[农学-畜牧学] 08[工学] 0817[工学-化学工程与技术] 09[农学] 070302[理学-分析化学] 0703[理学-化学] 

基  金:financially supported by Beijing Advanced Innovation Center for Food Nutrition and Human Health Basic Research Program of Science and Technology(2014FY111000) 

主  题:Colistin ELISA Feed Food Gold nanoparticle Lateral flow immunochromatographic assay Monoclonal antibody 

摘      要:Background:Colistin(polymyxin E)is a kind of peptide antibiotic which has been approved in animal production for the purposes of disease prevention,treatment,and growth ***,the wide use of colistin in animal feed may accelerate the spread of colistin-resistance gene MCR-1 from animal production to human beings,and its residue in animal-origin food may also pose serious health hazards to ***,it is necessary to develop corresponding analytical methods to monitor the addition of colistin in animal feed and the colistin residue in animal-origin ***:A one-step enzyme-linked immunosorbent assay(ELISA)and a lateral flow immunochromatographic assay(LFIA)for colistin were developed based on a newly developed monoclonal *** ELISA showed a 50%inhibition value(IC50)of 9.7 ng/m L with assay time less than 60 min,while the LFIA had a strip reader-based detection limit of 0.87 ng/m L in phosphate buffer with assay time less than 15 *** reducing the non-specific adsorption of colistin onto sample vial,the components of sample extraction solution were optimized and proved to greatly improve the assay *** spiked recovery experiment showed that the recoveries of colistin from feed,milk and meat samples were in the range of 77.83%to 113.38%with coefficient of variations less than 13%by ELISA analysis and less than 18%by LFIA analysis,***,actual sample analysis indicated that the two immunoassays can produce results consistent with instrumental ***:The developed assays can be used for rapid qualitative or quantitative detection of colistin in animal feed and food.

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