孙雪梅,许 强,孙晓萌,王轶鹏,张志涛,孟凡达.高效液相色谱法同时测定奶味饮料中的香兰素和乙基香兰素[J].食品安全质量检测学报,2020,11(17):6023-6027
高效液相色谱法同时测定奶味饮料中的香兰素和乙基香兰素
Simultaneous determination of vanillin and ethyl-vanillin in milk-taste-drink by high performance liquid chromatography
投稿时间:2020-07-03  修订日期:2020-07-15
DOI:
中文关键词:  高效液相色谱  食品添加剂  香兰素  乙基香兰素  快速检测
英文关键词:high performance liquid chromatography  food additive  vanillin  ethyl-vanillin  rapid analysis
基金项目:山东省医药卫生科技发展计划项目(2017WS075, 2015WS0196)
作者单位
孙雪梅 山东省医学科学院基础医学研究所, 山东第一医科大学 
许 强 山东省医学科学院基础医学研究所, 山东第一医科大学 
孙晓萌 山东省医学科学院基础医学研究所, 山东第一医科大学 
王轶鹏 山东省医学科学院基础医学研究所, 山东第一医科大学 
张志涛 山东省医学科学院基础医学研究所, 山东第一医科大学 
孟凡达 山东省医学科学院基础医学研究所, 山东第一医科大学 
AuthorInstitution
SUN Xue-Mei Institute of Basic Medicine, Shandong Academy of Medical Sciences, Shandong First Medical University 
XU Qiang Institute of Basic Medicine, Shandong Academy of Medical Sciences, Shandong First Medical University 
SUN Xiao-Meng Institute of Basic Medicine, Shandong Academy of Medical Sciences, Shandong First Medical University 
WANG Yi-Peng Institute of Basic Medicine, Shandong Academy of Medical Sciences, Shandong First Medical University 
ZHANG Zhi-Tao Institute of Basic Medicine, Shandong Academy of Medical Sciences, Shandong First Medical University 
MENG Fan-Da Institute of Basic Medicine, Shandong Academy of Medical Sciences, Shandong First Medical University 
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中文摘要:
      目的 建立高效液相色谱法同时测定奶味饮料中的香兰素和乙基香兰素的检测方法。方法 样品经含5%乙酸的乙腈溶液提取液提取, 超声处理后, 使用乙腈定容, 高速离心后上清液过0.22 μm微孔滤膜。使用高效液相色谱检测, 检测波长308 nm, 外标法定量。结果 本方法前处理简便易操作, 香兰素和乙基香兰素在0.1~100 μg/mL浓度范围内线性关系良好, 相关系数均大于0.999, 以3 S/N作为最低检出限, 方法的检出限均为0.02 μg/mL, 加标回收率分别为97.0%~101.1%、96.0%~100.5%, 相对标准偏差小于5%。结论 该方法操作简便, 准确度高, 重现性好, 适合奶味饮料中的香兰素和乙基香兰素的快速测定。
英文摘要:
      Objective To establish a simultaneous determination of vanillin and ethyl-vanillin in milk-taste-drink by high performance liquid chromatography. Methods The samples were extracted by acetonitrile with 5% acetic acid solution, after ultrasonic treatment, acetonitrile was used to fix the volume., Then determined by high performance liquid chromatography at 308 nm after high speed centrifugation and supernatant treatment. The external standard method was used for quantitative analysis. Results The pretreatment method was simple and easy to operate. The linear relationship between vanillin and ethyl vanillin was good in the concentration range of 0.1– 100 μg/mL, and the correlation coefficient was greater than 0.999. The detection limit of the method was 0.02 g/mL with 3 S/N as the lowest detection limit. The standard recovery was 97.0%–101.1% and 96.0%–100.5%, respectively, with the relative standard deviation less than 5%. Conclusion The method is simple, accurate and reproducible. It can be applied to the simultaneous determination of vanillin and ethyl-vanillin in milk-taste-drink.
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