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GPC结合GC-MS/MS法快速测定植物油中多环芳烃
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Determination of 16 polycyclic aromatic hydrocarbons in vegetable oil by GPC and GC-MS/MS
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    摘要:

    建立了凝胶渗透色谱(GPC)前处理技术结合气相色谱-串联质谱法(GC-MS/MS)检测植物油中16种多环芳烃含量的方法。结果表明:(1)添加16种多环芳烃的大豆油样品上GPC净化时其流出液采取分段收集的方法进行测定,0~19 min的流出液为油脂类杂质,19~28 min的流出液为前十种小分子量多环芳烃,28~36 min的流出液为后六种大分子量多环芳烃,说明凝胶渗透色谱并不是严格按照分子量大先出峰分子量小后出峰的顺序,在分离多种化合物时应该采用分段收集分段测定的方法才能保证结果的准确性;(2)与GB/T 23213—2008中前处理方法相比,通过将样品量从4 g减少到1 g,使用环己烷乙酸乙酯(1+1)溶解后直接上GPC净化的方法,减少了提取过程,缩短了实验时间,节约了提取试剂,避免了提取过程中可能造成的含量损失;(3)植物油中16种多环芳烃在GC-MS/MS上色谱峰响应值与其质量浓度(10~200 ng/mL)之间线性关系良好,相关系数超过0.99,检出限范围是0.02~0.50 μg/kg,定量限范围是0.08~1.67 μg/kg;(4)在16种多环芳烃标液添加水平为20 μL、40 μL、80 μL时16种多环芳烃平均回收率分别在85.30%~ 103.86%、91.08%~106.71%、88.01%~105.87%范围内,RSD分别0.69%~2.93%、0.64%~2.74%、0.75%~2.81%。该方法的精确度和灵敏度均能满足植物油中16种多环芳烃的测定。

    Abstract:

    A method for the determination of 16 polycyclic aromatic hydrocarbons in vegetable oil by gel permeation chromatography purification coupled with GC-MS/MS was developed. The results were shown below: (1) During GPC purification of soybean oil sample added with 16 PAHs, the distillates of 0~19 minutes were oil impurities. The distillates of 19~28 minutes and 28~36 minutes were collected in sections and then measured by GC-MS/MS. The results showed that the distillates from 19 to 28 minutes were PAHs of the first ten low molecular weight and the distillates from 28 to 36 minutes were PAHs of the last six high molecular weight. So, GPC was not strictly in the order of high molecular weight first peak and low molecular weight second peak. Therefore, in order to ensure the accuracy of the results, the method of segmenting collection and segmenting determination should be adopted when separating various compounds by GPC. (2) Compared with pretreatment method in GB/T 23213—2008, this method reduced the amount of vegetable oil sample weighed from 4.0 g to 1.0 g. The target analytes in samples were purified using GPC to eliminate most of the coextracts. The extraction process was simplified so that the possible content loss in the extraction process was avoided. The experiment time was shortened and the extraction reagent was saved. (3) The calibration curves of the 16 PAHs showed good linearity in the range of 10~200 ng/mL with the correlation coefficients(R2) greater than 0.99. The LOD ranged from 0.02 to 0.50μg/kg and LOQ ranged from 0.08 to 1.67 μg/kg for 16 PAHs. (4)At the spiked level of 20 μL, 40 μL and 80 μL the average recoveries were 85.30%~103.86%, 91.08%~106.71% and 88.01%~105.87% respectively, and relative standard deviations(RSDs) were 0.69%~2.93%, 0.64%~2.74% and 0.75%~2.81% respectively. The method met the requirements of 16 PAHs analysis.

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彭星星,高海军*,尹成华,刘 莹,戴冠苹,赵胜男,曹晶晶. GPC结合GC-MS/MS法快速测定植物油中多环芳烃[J].粮油食品科技,2022,30(6):138-146.

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  • 在线发布日期: 2022-11-22
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