Nguyen Thi Ha, Nguyen Bich, Le Phuong Thao, Tran Thi Hong, Nguyen Kieu
{"title":"Determination of Auramine O in animal feedstuffs using ultra performance liquid chromatography tandem mass spectrometry","authors":"Nguyen Thi Ha, Nguyen Bich, Le Phuong Thao, Tran Thi Hong, Nguyen Kieu","doi":"10.55401/sjbyqy53","DOIUrl":null,"url":null,"abstract":"A method based on ultra-high performance liquid chromatography coupled with tandem mass spectrometry (UPLC/MS/MS) was developed for simple and rapid determination of the residues of Auramine O in animal feedstuffs. The samples were extracted by MeOH: H2O + HCOOH 0.1% and then analyzed in multiple reaction monitoring (MRM) mode. The mobile phase was ultrapure water with 0.1% formic acid. Under the optimized detection conditions, the linear range for Auramine O was 20 - 100µg/L and the linear correlation coefficients found more than 0.99. The limit of quantification of Auramine O was 0.34 mg/kg. The recoveries of Auramine O ranged from 64.71 - 94.12% with relative standard deviations (RSD) of 4.93 - 8.31% with the concentration range of 20 - 100 µg/L. This method is simple, effective, sensitive and is suitable for the determination and confirmation of Auramine O in animal feedstuffs.","PeriodicalId":17073,"journal":{"name":"Journal of Science and Technology","volume":"323 2","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-01-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Science and Technology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.55401/sjbyqy53","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
A method based on ultra-high performance liquid chromatography coupled with tandem mass spectrometry (UPLC/MS/MS) was developed for simple and rapid determination of the residues of Auramine O in animal feedstuffs. The samples were extracted by MeOH: H2O + HCOOH 0.1% and then analyzed in multiple reaction monitoring (MRM) mode. The mobile phase was ultrapure water with 0.1% formic acid. Under the optimized detection conditions, the linear range for Auramine O was 20 - 100µg/L and the linear correlation coefficients found more than 0.99. The limit of quantification of Auramine O was 0.34 mg/kg. The recoveries of Auramine O ranged from 64.71 - 94.12% with relative standard deviations (RSD) of 4.93 - 8.31% with the concentration range of 20 - 100 µg/L. This method is simple, effective, sensitive and is suitable for the determination and confirmation of Auramine O in animal feedstuffs.