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超高效液相色谱法测定食品中的多种防腐剂
引用本文:凌云,储晓刚,张峰,陈琦,赵云峰,吴永宁,贾伟. 超高效液相色谱法测定食品中的多种防腐剂[J]. 中国卫生检验杂志, 2012, 0(2): 198-200,204
作者姓名:凌云  储晓刚  张峰  陈琦  赵云峰  吴永宁  贾伟
作者单位:中国疾病预防控制中心;中国检验检疫科学研究院;陕西科技大学
基金项目:北京市科技计划项目(D08050200310804,D08050200310803);财政部质检公益性行业科研项目(200910145)
摘    要:
目的:建立了超高效液相色谱(UPLC)法测定食品中14种防腐剂的定性定量分析方法。方法:样品用饱和氯化钠、乙腈、正己烷3种溶液萃取提取,正己烷提取溶液经凝胶渗透色谱(GPC)净化后与乙腈提取溶液合并注入超高效液相色谱分析。14种化合物经ACQUITY UPLCTMBEH C18柱(150 mm×2.1 mm,1.7μm)柱分离,以乙酸铵-乙腈溶液作为流动相进行梯度洗脱,紫外检测器(UV)检测,检测波长为280 nm。结果:14种化合物在线性范围内具有较好的线性关系,相关系数(r)>0.99,定量限(LOQ)在0.01 mg/kg~0.6 mg/kg之间;空白样品添加回收率在63.4%~99.5%之间,精密度(RSD)在0.490%~16.3%之间。结论:该方法适用于食品中防腐剂的检测。

关 键 词:超高效液相色谱法  防腐剂  凝胶渗透色谱  食品

Simultaneous determination of multiple preservatives in food using ultra performance liquid chromatography
LING Yun,CHU Xiao-gang,ZHANG Feng,CHEN Qi,ZHAO Yun-feng,WU Yong-ning,JIA Wei. Simultaneous determination of multiple preservatives in food using ultra performance liquid chromatography[J]. Chinses Journal of Health Laboratory Technology, 2012, 0(2): 198-200,204
Authors:LING Yun  CHU Xiao-gang  ZHANG Feng  CHEN Qi  ZHAO Yun-feng  WU Yong-ning  JIA Wei
Affiliation:2,3(1.Chinese Centre for Disease Control and Prevention,Beijing 100021,China;2.Chinese Academy of Inspection and Quarantine,Beijing 100123,China;3.Shanxi University of Science and Technology,Xi′an 710021,China)
Abstract:
Objective:An ultra performance liquid chromatography(UPLC) method was developed for the simultaneous determination of 14 preservatives in food.Methods: The samples were extracted using liquid-liquid extraction with saturated NaCl,acetonitrile and hexane.The extract in hexane was purified using GPC,and then combined with the extract in acetonitrile,finally,the mixed liquid was analyzed by UPLC.The analytes were separated on ACQUITY UPLCTM BEH C18 column using acetonitrile-ammonium acetate as mobile phase for gradient elution,then detected under UV detector with detection wavelength of 280 nm.Results: The correlation coefficient of this method had good linearity(r>0.99),the limits of quantification(LOQs) ranged from 0.01 mg/kg to 0.6 mg/kg.The recoveries at spiked levels ranged from 63.4% to 99.5%,the relative standard deviations(RSD) ranged from 0.490% to 16.3%.Conclusion: The method can be applied for the determination of preservatives in food.
Keywords:UPLC  Preservatives  GPC  Food
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