V. G. Amelin, I. V. Batov, O. I. Lavrukhina, A. V. Tretyakov, L. Kish
{"title":"Screening and simultaneous determination of 80 veterinary drugs residues in food by HPLC-MS/MS","authors":"V. G. Amelin, I. V. Batov, O. I. Lavrukhina, A. V. Tretyakov, L. Kish","doi":"10.26896/1028-6861-2023-89-8-12-22","DOIUrl":null,"url":null,"abstract":"<jats:p>A<jats:bold> </jats:bold>fast<jats:bold> </jats:bold>method<jats:bold> </jats:bold>of<jats:bold> </jats:bold>samples<jats:bold> </jats:bold>screening<jats:bold> </jats:bold>and<jats:bold> </jats:bold>determination<jats:bold> </jats:bold>of<jats:bold> </jats:bold>80<jats:bold> </jats:bold>veterinary<jats:bold> </jats:bold>drugs<jats:bold> </jats:bold>residues<jats:bold> </jats:bold>in<jats:bold> </jats:bold>food<jats:bold> </jats:bold>safety<jats:bold> </jats:bold>assessment<jats:bold> </jats:bold>is<jats:bold> </jats:bold>proposed.<jats:bold> </jats:bold>The<jats:bold> </jats:bold>solid-phase<jats:bold> </jats:bold>extraction<jats:bold> </jats:bold>for<jats:bold> </jats:bold>the<jats:bold> </jats:bold>extract<jats:bold> </jats:bold>purification<jats:bold> </jats:bold>in<jats:bold> </jats:bold>the<jats:bold> </jats:bold>sample<jats:bold> </jats:bold>preparation<jats:bold> </jats:bold>is<jats:bold> </jats:bold>excluded,<jats:bold> </jats:bold>at<jats:bold> </jats:bold>the<jats:bold> </jats:bold>same<jats:bold> </jats:bold>time<jats:bold> </jats:bold>the<jats:bold> </jats:bold>matrix<jats:bold> </jats:bold>effect<jats:bold> </jats:bold>is<jats:bold> </jats:bold>mitigated<jats:bold> </jats:bold>by<jats:bold> </jats:bold>the<jats:bold> </jats:bold>isotope-labeled<jats:bold> </jats:bold>standards<jats:bold> </jats:bold>using.<jats:bold> </jats:bold>The<jats:bold> </jats:bold>isotope<jats:bold> </jats:bold>dilution<jats:bold> </jats:bold>method<jats:bold> </jats:bold>allowed<jats:bold> </jats:bold>to<jats:bold> </jats:bold>exclude<jats:bold> </jats:bold>matrix<jats:bold> </jats:bold>calibration<jats:bold> </jats:bold>curves<jats:bold> </jats:bold>construction<jats:bold> </jats:bold>and<jats:bold> </jats:bold>calculate<jats:bold> </jats:bold>the<jats:bold> </jats:bold>concentration<jats:bold> </jats:bold>using<jats:bold> </jats:bold>correction<jats:bold> </jats:bold>coefficients<jats:bold> </jats:bold>found<jats:bold> </jats:bold>from<jats:bold> </jats:bold>analytes<jats:bold> </jats:bold>standard<jats:bold> </jats:bold>aqueous<jats:bold> </jats:bold>solutions<jats:bold> </jats:bold>and<jats:bold> </jats:bold>a<jats:bold> </jats:bold>limited<jats:bold> </jats:bold>number<jats:bold> </jats:bold>of<jats:bold> </jats:bold>isotope-labeled<jats:bold> </jats:bold>standards.<jats:bold> </jats:bold>The<jats:bold> </jats:bold>drugs<jats:bold> </jats:bold>residues<jats:bold> </jats:bold>limits<jats:bold> </jats:bold>of<jats:bold> </jats:bold>detection<jats:bold> </jats:bold>(<jats:italic>c</jats:italic><jats:sub>min</jats:sub><jats:bold> </jats:bold>=<jats:bold> </jats:bold>0,1<jats:bold> </jats:bold>–<jats:bold> </jats:bold>10<jats:bold> </jats:bold>ng/g)<jats:bold> </jats:bold>allowed<jats:bold> </jats:bold>their<jats:bold> </jats:bold>determination<jats:bold> </jats:bold>at<jats:bold> </jats:bold>the<jats:bold> </jats:bold>maximum<jats:bold> </jats:bold>permissible<jats:bold> </jats:bold>levels<jats:bold> </jats:bold>for<jats:bold> </jats:bold>food.</jats:p>","PeriodicalId":13559,"journal":{"name":"Industrial laboratory. Diagnostics of materials","volume":"36 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-08-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Industrial laboratory. Diagnostics of materials","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.26896/1028-6861-2023-89-8-12-22","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
食品中80种兽药残留的HPLC-MS/MS筛选与同时测定
提出了一种食品安全评价中80种兽药残留的快速筛选和检测方法。排除了样品制备中萃取物纯化的固相萃取,同时采用同位素标记标准物减轻了基质效应。同位素稀释法允许排除矩阵校准曲线的构建,并使用从分析物标准水溶液和有限数量的同位素标记标准中找到的校正系数来计算浓度。药物残留检测限(cmin = 0.1 - 10 ng/g)使其能够在食品中达到最大允许水平。
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