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固相萃取-高效液相色谱法测定水果和果酱中的6种对羟基苯甲酸酯
引用本文:陈皑,何乔桑,王萍亚,周勇,黄鹂,许镇坚,赵华,张薇英.固相萃取-高效液相色谱法测定水果和果酱中的6种对羟基苯甲酸酯[J].色谱,2009,27(6):804-808.
作者姓名:陈皑  何乔桑  王萍亚  周勇  黄鹂  许镇坚  赵华  张薇英
作者单位:1.National Marine Food Quality Supervision and Testing Center, Zhoushan 316021, China; 2.Zhejiang Province Food Quality and Safety Test Center, Hangzhou 310013, China
基金项目:浙江省重大科技计划项目 
摘    要:建立了固相萃取-高效液相色谱(SPE-HPLC)同时测定水果和果酱中6种对羟基苯甲酸酯(对羟基苯甲酸甲酯、对羟基苯甲酸乙酯、对羟基苯甲酸异丙酯、对羟基苯甲酸丙酯、对羟基苯甲酸异丁酯和对羟基苯甲酸丁酯)含量的方法。经Oasis HLB固相萃取柱净化的样品采用HPLC分离,优化的色谱条件为采用Symmetry-C18色谱柱分离,流动相为柠檬酸缓冲液-甲醇(体积比为48:52),流速1.0 mL/min,检测波长258 nm,测定温度40 ℃。6种对羟基苯甲酸酯的线性范围为0.1~20.0 mg/L(r=0.9999),回收率为82.8%~115.5%,相对标准偏差为0.2%~6.8%(n=6)。对羟基苯甲酸甲酯、对羟基苯甲酸乙酯、对羟基苯甲酸异丙酯、对羟基苯甲酸丙酯的检出限(S/N=3)为0.1 mg/kg,定量限(S/N=10)为0.3 mg/kg;对羟基苯甲酸异丁酯和对羟基苯甲酸丁酯的检出限为0.2 mg/kg,定量限为0.6 mg/kg。该方法简便快速、结果准确、重现性好,可作为测定水果及果酱中多种对羟基苯甲酸酯的有效方法。

关 键 词:对羟基苯甲酸酯  高效液相色谱法  固相萃取  果酱  水果  
收稿时间:2009-7-16
修稿时间:2009-9-16

Determination of six p-hydroxybenzoates in fruits and jams using solid-phase extraction-high performance liquid chromatography
CHEN Ai,HE Qiaosang,WANG Pingya,ZHOU Yong,HUANG Li,XU Zhenjian,ZHAO Hua,ZHANG Weiying.Determination of six p-hydroxybenzoates in fruits and jams using solid-phase extraction-high performance liquid chromatography[J].Chinese Journal of Chromatography,2009,27(6):804-808.
Authors:CHEN Ai  HE Qiaosang  WANG Pingya  ZHOU Yong  HUANG Li  XU Zhenjian  ZHAO Hua  ZHANG Weiying
Institution:1.National Marine Food Quality Supervision and Testing Center, Zhoushan 316021, China; 2.Zhejiang Province Food Quality and Safety Test Center, Hangzhou 310013, China
Abstract:A method was developed for the determination of 6 p-hydroxybenzoates (methyl p-hydroxybenzoate (MHB), ethyl p-hydroxybenzoate (EHB), isopropyl p-hydroxybenzoate (IPHB), propyl p-hydroxybenzoate (PHB), isobutyl p-hydroxybenzoate (IBHB) and butyl p-hydroxybenzoate (BHB)) in fruits and jams using the combination of solid-phase extraction and high performance liquid chromatography (SPE-HPLC). Two different extraction solutions and three different mobile phases were tested for p-hydroxybenzoates analysis, and finally ethanol was used as the extraction solvent and methanol-citric acid buffer was selected as the mobile phase. The sample was extracted, and purified by an Oasis HLB solid-phase extraction cartridge, then separated on a Symmetry-C18 column and detected at the wave length of 258 nm. The results showed that all the calibration graphs were linear in the concentration range of 0.1~20.0 mg/L (r=0.9999). The detection limits and quantification limits were 0.1 mg/kg (S/N=3) and 0.3 mg/kg (S/N=10) respectively for MHB, EHB, IPHB and PHB, 0.2 mg/kg (S/N=3) and 0.6 mg/kg (S/N=10) respectively for IBHB and BHB. The average recoveries were between 82.8% and 115.5% with the relative standard deviations (RSDs) of 0.2%~6.8%(n=6). The method is simple, rapid, sensitive and reproducible, and can be used for the routine analysis of the p-hydroxybenzoates in fruits and jams.
Keywords:solid phase extraction (SPE)  high performance liquid chromatography (HPLC)  p-hydroxybenzoates  fruits  jams
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