色谱

色谱

• 研究论文 • 上一篇    下一篇

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

陈皑1, 何乔桑2, 王萍亚1*, 周勇1, 黄鹂1, 许镇坚1, 赵华1, 张薇英1   

  1. 1.National Marine Food Quality Supervision and Testing Center, Zhoushan 316021, China; 2.Zhejiang Province Food Quality and Safety Test Center, Hangzhou 310013, China
  • 收稿日期:2009-07-16 修回日期:2009-09-16 出版日期:2009-11-30 发布日期:1981-12-25
  • 通讯作者: 王萍亚

Determination of six p-hydroxybenzoates in fruits and jams using solid-phase extraction-high performance liquid chromatography

CHEN Ai1, HE Qiaosang2, WANG Pingya1*, ZHOU Yong1, HUANG Li1, XU Zhenjian1, ZHAO Hua1, ZHANG Weiying1   

  1. 1.National Marine Food Quality Supervision and Testing Center, Zhoushan 316021, China; 2.Zhejiang Province Food Quality and Safety Test Center, Hangzhou 310013, China
  • Received:2009-07-16 Revised:2009-09-16 Online:2009-11-30 Published:1981-12-25
  • Contact: WANG Pingya

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1334

被引次数

47

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

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.

Key words: fruits, high performance liquid chromatography (HPLC), jams , p-hydroxybenzoates, solid phase extraction (SPE)