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食品研究与开发:2021,42(2):173-177
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超高效液相色谱-串联质谱法检测牛组织中常山酮残留量
(漯河食品职业学院,河南 漯河 462300)
Determination of Halofuginone in Bovine Tissues by Ultra Performance Liquid Chromatography-Tandem Mass Spectrometry
(Luohe Vocational College of Food,Luohe 462300,Henan,China)
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投稿时间:2020-08-01    
中文摘要: 为了建立牛组织中常山酮残留量的超高效液相色谱-串联质谱检测方法,将牛组织中的常山酮经蛋白酶酶解后,采用乙酸乙酯提取,HLB固相萃取柱净化,超高效液相色谱-串联质谱法进行检测。在0.5 ng/mL~50 ng/mL线性范围内,常山酮的回归方程呈良好的线性关系,R2>0.998,牛组织样品在添加水平为0.5、5 μg/kg时,回收率为73.2%~93.60%,相对标准偏差(relative standard deviation,RSD)为 5.91%~7.96%,方法检出限为 0.25 μg/kg,定量限为 0.5 μg/kg。本试验适用于牛组织中常山酮残留量的检测。
Abstract:To develop a method for determination of halofuginone in bovine tissues by ultra performance liquid chromatography-tandem mass spectrometry(UPLC-MS/MS).Bovine tissues samples were enzymolysed with trypsin,and extracted with ethyl acetate,then cleaned up with SPE column.Finally,the analytes were tested by UPLC-MS/MS.The matrix-matched calibration curve of halofuginone showed a good linear within the concentration range from 0.5 ng/mL to 50 ng/mL (R2>0.998).In the bovine tissues samples,the recovery of halofuginone at the spiked levels of 0.5,5 μg/kg was from 73.2% to 93.60%,and the relative standard deviation(RSD)was between 5.91% and 7.96%,and the limit of detection was 0.25 μg/kg,the limit of quantitation was 0.5 μg/kg.The method is suitable for the detection of halofuginone in bovine tissues.
文章编号:202102028     中图分类号:    文献标志码:
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