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高效液相色谱法测定软饮料中香兰素和乙基香兰素
引用本文: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].食品安全质量检测技术,2015,6(1):152-158.
作者姓名:肖珊珊  孙兴权  李一尘  王 璇  王昕璐  赵红玲  刘慧颖  曹际娟
作者单位:辽宁出入境检验检疫局,辽宁出入境检验检疫局,辽宁出入境检验检疫局,塔城出入境检验检疫局,大连工业大学,辽宁出入境检验检疫局,辽宁出入境检验检疫局,辽宁出入境检验检疫局
基金项目:辽宁出入境检验检疫局自主立项项目(LK26-2010)
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/m L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。

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
收稿时间:2014/11/18 0:00:00
修稿时间:1/6/2015 12:00:00 AM

Determination of vanillin and ethyl vanillin in soft drink by high performance liquid chromatography
XIAO Shan-Shan,SUN Xing-Quan,LI Yi-Chen,WANG Xuan,WANG Xin-Lu,ZHAO Hong-Ling,LIU Hui-Ying and CAO Ji-Juan.Determination of vanillin and ethyl vanillin in soft drink by high performance liquid chromatography[J].Food Safety and Quality Detection Technology,2015,6(1):152-158.
Authors:XIAO Shan-Shan  SUN Xing-Quan  LI Yi-Chen  WANG Xuan  WANG Xin-Lu  ZHAO Hong-Ling  LIU Hui-Ying and CAO Ji-Juan
Affiliation:Liaoning Entry-Exit Inspection and Quarantine Bureau,Liaoning Entry-Exit Inspection and Quarantine Bureau,Liaoning Entry-Exit Inspection and Quarantine Bureau,Tacheng Entry-Exit Inspection and Quarantine Bureau,Dalin Polytechnic University,Liaoning Entry-Exit Inspection and Quarantine Bureau,Liaoning Entry-Exit Inspection and Quarantine Bureau and Liaoning Entry-Exit Inspection and Quarantine Bureau
Abstract: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.
Keywords:food additive  spice  soft drink  vanillin  ethyl vanillin  QuEChERS  high performance liquid chromatography
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