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    望秀丽, 全王榫, 李志豪. 超高效液相色谱法测定食品接触材料中抗氧剂245的迁移量[J]. 理化检验-化学分册, 2024, 60(8): 832-836. DOI: 10.11973/lhjy-hx220692
    引用本文: 望秀丽, 全王榫, 李志豪. 超高效液相色谱法测定食品接触材料中抗氧剂245的迁移量[J]. 理化检验-化学分册, 2024, 60(8): 832-836. DOI: 10.11973/lhjy-hx220692
    WANG Xiuli, QUAN Wangsun, LI Zhihao. Determination of Migration of Irganox 245 from Food Contact Materialsby Ultra-High Performance Liquid Chromatography[J]. PHYSICAL TESTING AND CHEMICAL ANALYSIS PART B:CHEMICAL ANALYSIS, 2024, 60(8): 832-836. DOI: 10.11973/lhjy-hx220692
    Citation: WANG Xiuli, QUAN Wangsun, LI Zhihao. Determination of Migration of Irganox 245 from Food Contact Materialsby Ultra-High Performance Liquid Chromatography[J]. PHYSICAL TESTING AND CHEMICAL ANALYSIS PART B:CHEMICAL ANALYSIS, 2024, 60(8): 832-836. DOI: 10.11973/lhjy-hx220692

    超高效液相色谱法测定食品接触材料中抗氧剂245的迁移量

    Determination of Migration of Irganox 245 from Food Contact Materialsby Ultra-High Performance Liquid Chromatography

    • 摘要: 以水、4%(体积分数,下同)乙酸溶液、10%(体积分数,下同)乙醇溶液、20%(体积分数,下同)乙醇溶液、50%(体积分数,下同)乙醇溶液、95%(体积分数,下同)乙醇溶液和异辛烷作食品模拟物,按照GB 5009.156—2003和GB 31604.1—2015进行迁移试验。前5种食品模拟物的浸泡液用0. 22 μm有机滤膜过滤后,滤液上机测定。分取10 mL 95%乙醇溶液浸泡液,于50 ℃旋蒸至近干,分两次加入8 mL 80%(体积分数,下同)甲醇溶液溶解残渣并稀释至10 mL,上机测定;分取10 mL异辛烷浸泡液,加入10 mL 80%甲醇溶液,摇动约1 min混匀,静置约30 min,收集下层相并用80%甲醇溶液稀释至10 mL,过0. 22 μm有机滤膜,滤液上机测定。在超高效液相色谱法分析中,采用ACQUITY UPLC BEH C18色谱柱作固定相,80%甲醇溶液为流动相进行等度洗脱,在220 nm检测波长下采用二极管阵列检测器测定抗氧剂245的含量。结果显示,抗氧剂245的质量浓度在0. 5~10. 0 mg·L−1内和峰面积呈线性关系,测定下限为0. 14~0. 30 mg·L−1。按照标准加入法进行回收试验,回收率为86. 4%~104%,测定值的相对标准偏差(n=6)为2. 0%~5. 4%。方法用于不同材质食品接触材料样品的分析,仅在聚甲醛(POM)盖样品中检出了抗氧剂245,在不同食品模拟物中的迁移量由大到小排序为50%乙醇溶液、95%乙醇溶液、20%乙醇溶液、10%乙醇溶液和4%乙酸溶液。

       

      Abstract: Using water, 4% (volume fraction, the same below) acetic acid solution, 10% (volume fraction, the same below) ethanol solution, 20% (volume fraction, the same below) ethanol solution, 50% (volume fraction, the same below) ethanol solution, 95% (volume fraction, the same below) ethanol solution, and isooctane as food simulants, tests for migration were conducted according to GB 5009.156—2003 and GB 31604.1—2015. The soaking solutions of the first five food simulants were filtered by a 0.22 μm organic filter membrane, and the filtrate was determined by the instrument. An aliquot (10 mL) of soaking solution of 95% ethanol solution was taken and evaporated to near dryness at 50 ℃, and 8 mL of 80% (volume fraction, the same below) methanol solution was added twice to dissolve the residue. The solution obtained was diluted to 10 mL by 80% methanol solution for determination by the instrument. An aliquot (10 mL) soaking solution of isooctane was taken, and 10 mL of 80% methanol solution was added. After shaking well for about 1 min, the solution obtained was settled for about 30 min. The lower layer phase was collected, and diluted to 10 mL by 80% methanol solution. The resulting solution was passed through a 0.22 μm organic filter membrane, and the filtrate was determined by the instrument. In the analysis of ultra-high performance liquid chromatography, the ACQUITY UPLC BEH C18 chromatographic column was used as the stationary phase, and 80% methanol solution was used as the mobile phase for isocratic elution. The content of irganox 245 was determined by the diode array detector at detection wavelength of 220 nm. It was shown that linear relationships between values of the mass concentration and the peak area of irganox 245 were kept in the range of 0.5-10.0 mg·L−1, with lower limit of determination of 0.14-0.30 mg·L−1. Test for recovery was made according to the standard addition method, giving recoveries in the range of 86.4%-104%, and RSDs (n=6) of the determined values ranged from 2.0% to 5.4%. The proposed method was used for the analysis of samples of food contact materials with different matrices, and irganox 245 was only detected in polyoxymethylene (POM) cap samples. The migration amounts in different food simulants were ranked from high to low as 50% ethanol solution, 95% ethanol solution, 20% ethanol solution, 10% ethanol solution, and 4% acetic acid solution.

       

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