首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Simultaneous determination of total fatty acid esters of chloropropanols in edible oils by gas chromatography-mass spectrometry with solid-supported liquid-liquid extraction
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Simultaneous determination of total fatty acid esters of chloropropanols in edible oils by gas chromatography-mass spectrometry with solid-supported liquid-liquid extraction

机译:固相固液萃取-气相色谱-质谱法同时测定食用油中氯丙醇总脂肪酸酯

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摘要

This study aimed to establish a novel robust method for the simultaneous determination of total fatty acid esters of 4 chloropropanols including fatty acid esters of 3-monochloropropane-1,2-diol (3-MCPD esters), 2-monochloropropane-1,3-diol (2-MCPD esters), 1,3-dichloropropan-2-ol (1,3-DCP esters) and 2,3-dichloropropan-1-ol (2,3-DCP esters) in edible oils. In this method, sodium methylate in methanol was used as the reagent for the ester cleavage reaction of chloropropanols esters. The reaction products were extracted by a sodium sulfate solution, and then purified by solid-supported liquid-liquid extraction (SLE) using diatomaceous earth (Hydromatrix?) as the sorbent. Finally, the extracts were derivatized with heptafluorobutyrylim idazole (HFBI) and analyzed by gas chromatography-mass spectrometry (GC-MS). Quantification was achieved using deuterated chloropropanols as their respective internal standards, including 3-MCPD-d_5, 2-MCPD-d_5, 1,3-DCP-d_5 and 2,3-DCP-d_5. A good linear relationship between peak area and concentrations was obtained within the range of 0.025-2.000mgL~(-1) with a correlation coefficients not less than 0.999 for all the chloropropanols esters. The limits of detection (LODs) of esters of 3-MCPD, 2-MCPD, 1,3-DCP and 2,3-DCP (calculated as corresponding chloropropanols) were 30, 30, 100 and 30μgkg-1, respectively. The average recoveries of the 3-MCPD esters and the 4 chloropropanols spiked at 0.1, 0.5 and 2mgkg-1 into blank oil matrix were typically in a range from 70.7% to 113.3%. The robust method validation data including calibration, LOD/LOQ, accuracy and repeatability and proficiency test results (Z-score: -0.5) of the official Food Analysis Performance Assessment Scheme (FAPAS) indicated that the present quantitative method could be successfully applied to the determination of total chloropropanols esters in various edible oils.
机译:这项研究旨在建立一种同时测定4种氯丙醇总脂肪酸酯(包括3-一氯丙烷-1,2-二醇的脂肪酸酯(3-MCPD酯),2-一氯丙烷-1,3-的脂肪酸酯)的可靠方法。食用油中的二醇(2-MCPD酯),1,3-二氯丙烷-2-醇(1,3-DCP酯)和2,3-二氯丙烷-1-醇(2,3-DCP酯)。在该方法中,使用甲醇中的甲醇钠作为氯丙醇酯的酯裂解反应的试剂。用硫酸钠溶液萃取反应产物,然后使用硅藻土(Hydromatrix?)作为吸附剂,通过固相支持的液-液萃取(SLE)纯化。最后,将提取物用七氟丁酰咪唑(HFBI)衍生化并通过气相色谱-质谱(GC-MS)分析。使用氘代氯丙醇作为各自的内标(包括3-MCPD-d_5、2-MCPD-d_5、1,3-DCP-d_5和2,3-DCP-d_5)进行定量。在所有氯丙醇酯的0.025-2.000mgL〜(-1)范围内,峰面积与浓度之间具有良好的线性关系,相关系数不小于0.999。 3-MCPD,2-MCPD,1,3-DCP和2,3-DCP(按相应的氯丙醇计算)的酯的检出限(LOD)分别为30、30、100和30μgkg-1。分别向空白油基质中加入0.1、0.5和2mgkg-1的3-MCPD酯和4种氯丙醇的平均回收率通常在70.7%至113.3%的范围内。官方食品分析性能评估计划(FAPAS)的可靠方法验证数据包括校准,LOD / LOQ,准确性和可重复性以及能力验证结果(Z评分:-0.5)表明,本定量方法可以成功地应用于食品分析绩效评估。测定各种食用油中的总氯丙醇酯。

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