首页|HPLC-MS/MS测定茶叶中灭草松及其代谢物残留量

HPLC-MS/MS测定茶叶中灭草松及其代谢物残留量

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探索QuEChERS-液相色谱-质谱联用法,建立一种测定茶叶中灭草松及其代谢物6-羟基灭草松、8-羟基灭草松残留量的方法.用水浸泡茶叶样品一段时间后,用1%的乙酸乙腈溶液提取,经无水硫酸镁、PSA、C18、GCB进行混合净化,采用液相色谱-质谱法和多反应监测(MRM)模式检测及外标法对茶叶中的灭草松及其代谢物6-羟基灭草松、8-羟基灭草松残留进行定量分析.在优化条件下,灭草松及其代谢物具有良好的线性关系(在1~100 μg/L范围内,r>0.99),在10,20和100 μg/kg这3个水平的加标下,样品平均回收率为83.4%~99.2%,相对标准偏差(n=6)为1.2%~7.3%,方法检出限为0.014~0.42 μg/kg,定量限为10 μg/kg.该方法适用于茶叶中灭草松及其代谢物的同时检测.
Determination of Residues of Bentazone and Its Metabolites in Tea by HPLC-MS/MS
A QuEChERS-liquid chromatography-mass spectrometry(LC-MS/MS)method was established a method for the determination of bentazone and its metabolites(6-hydroxymetazone and 8-hydroxymetazone residues)in tea.The tea samples were soaked in water for a period of time,extracted with 1%acetonitrile acetate solution as following,then purified by the mixed purification PSA,C18,GCB with anhydrous magnesium sulfate,and detected by liquid chromatography-mass spectrometry(LC-MS/MS)in multi-reaction monitoring(MRM)mode for the residues of methomyl and its metabolites named 6-hydroxymetazone and 8-hydroxymetazone in tea,as well as quantified by external standard method.Good linearity(r>0.99)was observed in the range of 1-100 μg/L for mace and its metabolites under the optimized condition,and the average recoveries of the samples were 83.4%-99.2%with the relative standard deviation(n=6).f 1.2%-7.3%,the limits of detection of the method were 0.014-0.42 μg/kg and the limits of quantification were 10 μg/kg at three spiked levels(10,20 and 100 μg/kg).It's not hard to make the conclusion that the method is suitable for the simultaneous determination of bentazone and its metabolites in tea.

liquid chromatography-tandem mass spectrometry(HPLC-MS/MS)QuEChERStearesidues

吴晓萍

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福建中检华日食品安全检测有限公司(福州 350028)

液相色谱-串联质谱(LC-MS/MS) QuEChERS 茶叶 残留

2024

食品工业
上海市食品工业研究所

食品工业

影响因子:0.47
ISSN:1004-471X
年,卷(期):2024.45(3)
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