首页> 外文期刊>LWT-Food Science & Technology >Simultaneous determination of 3-MCPD fatty acid esters and glycidol fatty acid esters in edible oils using liquid chromatography time-of-flight mass spectrometry.
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Simultaneous determination of 3-MCPD fatty acid esters and glycidol fatty acid esters in edible oils using liquid chromatography time-of-flight mass spectrometry.

机译:使用液相色谱飞行时间质谱仪同时测定食用油中的3-MCPD脂肪酸酯和缩水甘油脂肪酸酯。

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A liquid chromatography time-of-flight mass spectrometry (LC/TOF-MS) method was developed for the simultaneous determination of 3-chloropropane-1,2-diol fatty acid esters (3-MCPDEs) and glycidol fatty acid esters (GEs) in edible oils. Three species of 3-MCPD monoesters, six species of 3-MCPD diesters, and five species of GE were evaluated. The analytes were extracted by solid-phase extraction and were eluted through a Waters UPLC C18 chromatography column with a gradient mobile phase of methanol containing sodium formate. The detection was performed by selected ion monitoring for the respective sodiated adducts of the target compounds. The system was precise (with relative standard deviation (RSD) of retention time below 1.7%) and sensitive, with a limit of detection (LOD) of less than 0.16 ng/mL for GEs, 0.86 ng/mL for 3-MCPD monoesters, and 0.22 ng/mL for 3-MCPD diesters. The recoveries of GEs and 3-MCPDEs from oil samples were in the range of 62.6-108.8%, with RSD ranging between 1.5 and 11.3%. The method has been successfully applied to determine these compounds in edible oil samples. All rights reserved, Elsevier.
机译:建立了液相色谱飞行时间质谱(LC / TOF-MS)方法,用于同时测定3-氯丙烷-1,2-二醇脂肪酸酯(3-MCPDEs)和缩水甘油脂肪酸酯(GEs)的方法在食用油中。评估了3种3-MCPD单酯,6种3-MCPD二酯和5种GE。通过固相萃取法提取分析物,并通过Waters UPLC C 18 色谱柱进行洗脱,该色谱柱使用含有甲酸钠的甲醇梯度流动相洗脱。通过选择离子监测对目标化合物的各个磺化加合物进行检测。该系统精密(保留时间的相对标准偏差(RSD)低于1.7%)且灵敏,GE的检测下限(LOD)小于0.16 ng / mL,3-MCPD单酯的检测下限(0.86 ng / mL), 3-MCPD二酯为0.22 ng / mL。从油样中回收的GE和3-MCPDE的回收率在62.6-108.8%之间,RSD在1.5和11.3%之间。该方法已成功应用于测定食用油样品中的这些化合物。保留所有权利,Elsevier。

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