肖珊珊,孙兴权,李一尘,王 璇,王昕璐,赵红玲,刘慧颖,曹际娟.高效液相色谱法测定软饮料中香兰素和乙基香兰素[J].食品安全质量检测学报,2015,6(1):152-158
高效液相色谱法测定软饮料中香兰素和乙基香兰素
Determination of vanillin and ethyl vanillin in soft drink by high performance liquid chromatography
投稿时间:2014-11-18  修订日期:2015-01-06
DOI:
中文关键词:  食品添加剂  香料  软饮料  香兰素  乙基香兰素  QuEChERS  高效液相色谱法
英文关键词:food additive  spice  soft drink  vanillin  ethyl vanillin  QuEChERS  high performance liquid chromatography
基金项目:辽宁出入境检验检疫局自主立项项目(LK26-2010)
作者单位
肖珊珊 辽宁出入境检验检疫局 
孙兴权 辽宁出入境检验检疫局 
李一尘 辽宁出入境检验检疫局 
王 璇 塔城出入境检验检疫局 
王昕璐 大连工业大学 
赵红玲 辽宁出入境检验检疫局 
刘慧颖 辽宁出入境检验检疫局 
曹际娟 辽宁出入境检验检疫局 
AuthorInstitution
XIAO Shan-Shan Liaoning Entry-Exit Inspection and Quarantine Bureau 
SUN Xing-Quan Liaoning Entry-Exit Inspection and Quarantine Bureau 
LI Yi-Chen Liaoning Entry-Exit Inspection and Quarantine Bureau 
WANG Xuan Tacheng Entry-Exit Inspection and Quarantine Bureau 
WANG Xin-Lu Dalin Polytechnic University 
ZHAO Hong-Ling Liaoning Entry-Exit Inspection and Quarantine Bureau 
LIU Hui-Ying Liaoning Entry-Exit Inspection and Quarantine Bureau 
CAO Ji-Juan Liaoning Entry-Exit Inspection and Quarantine Bureau 
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中文摘要:
      目的 建立软饮料中香兰素和乙基香兰素的高效液相色谱法检测方法。方法 样品中的香兰素和乙基香兰素在酸性条件下经乙腈提取, 利用盐析作用分层净化, 提取液浓缩复溶解后, 供液相色谱检测。检测波长308 nm, 外标法定量。结果 香兰素和乙基香兰素在0.5~50.0 ?g/mL浓度范围内线性关系良好, 相关系数均大于0.9999。添加水平为5、30、63 mg/kg时, 香兰素和乙基香兰素的平均回收率分别为98.4%和100.4%, 96.7%和100.2%, 97.8%和100.3%, 相对标准偏差在3.53%~4.70%, 检出限均为0.5 mg/kg。结论 方法操作简便、快速, 经济实用, 适用性强, 结果准确可靠, 可用于样品批量快速检测。
英文摘要:
      Objective To develop a method for determination of vanillin and ethyl vanillin in soft drink by high performance liquid chromatography (HPLC). Methods Vanillin and ethyl vanillin in sample were extracted with acetonitrile and 0.1% formic acid solution, and were cleaned up by salting out effect. After concentrated, the extraction was redissolved and determined by HPLC at 308 nm. The external standard method was used for quantitative analysis. Results The method showed a good linear over the range of 0.5~50.0 ?g/mL for vanillin and ethyl vanillin with correlation coefficients above 0.9999. The average recoveries were 98.4% and 100.4%, 96.7% and 100.2%, 97.8% and 100.3% at the spiked level of 5, 30, and 63 mg/kg, with relative standard deviation between 3.53%~4.70%. The limit of detection was 0.5 mg/kg. Conclusion The method is simple, rapid, economical and practical, and the result is accurate and reliable, which is suitable for batch sample determination.
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