食品科学 ›› 2010, Vol. 31 ›› Issue (16): 161-164.doi: 10.7506/spkx1002-6630-201016033

• 分析检测 • 上一篇    下一篇

离子液体修饰玻碳电极测定金银花中的总黄酮

李红波1,2,金根娣2,杜 诗2,任艳艳2,胡效亚2   

  1. 1.盐城工学院化学与生物工程学院 2.扬州大学化学化工学院
  • 收稿日期:2009-12-10 修回日期:2010-05-17 出版日期:2010-08-25 发布日期:2010-12-29
  • 通讯作者: 李红波 E-mail:lhbchem@163.com
  • 基金资助:

    国家自然科学基金项目(20675071;20875081);盐城工学院自然科学基金项目(XKY2009009)

Determination of Total Flavonoids in Flos Ionicera Using Ion Liquid Modified Glassy Carbon Electrode

LI Hong-bo1,2,JIN Gen-di2,DU Shi2,REN Yan-yan2,HU Xiao-ya2   

  1. 1. School of Chemistry and Biological Engineering, Yancheng Institute of Technology
    2. College of Chemistry and Chemical Engineering, Yangzhou University
  • Received:2009-12-10 Revised:2010-05-17 Online:2010-08-25 Published:2010-12-29
  • Contact: LI Hong-bo E-mail:lhbchem@163.com

摘要:

用1- 丁基-3- 甲基咪唑六氟磷酸盐([BMIM]PF6)疏水性离子液体作修饰剂制作[BMIM]PF6- 修饰玻碳电极。在0.2mol/L 磷酸盐缓冲液(pH7.0)中,运用差示脉冲溶出伏安法(DPSV)研究木犀草素在修饰电极上的电化学行为,建立测定金银花中总黄酮含量的新方法。研究表明,该修饰电极降低了木犀草素的氧化还原峰电位,增大了其氧化还原反应的峰电流。木犀草素氧化峰电流与其浓度在1.0 × 10-10~1.6 × 10-8mol/L 范围内呈良好的线性关系,检出限达到3.2 × 10-11mol/L,回收率为98.7%~103.6%。该法操作简单、快速、灵敏、准确,可用于金银花中总黄酮的测定。

关键词: 木犀草素, 离子液体, 修饰电极, 总黄酮, 电化学

Abstract:

A glassy carbon electrode modified with hydrophobicity 1-n-butyl-3-methylimidazolium hexafluorophosphate ([BMIM]PF6/GCE) was fabricated. Differential pulse stripping voltammetry was used to investigate the electrochemical behavior of luteolin at the modified electrode in 0.2 mol/L phosphate buffer solution, pH 7.0 and a new method for determining total flavonoids in Flos Ionicera was established. It was found that the peak potentials for oxidation and reduction both shifted negatively by 15 mV at the modified electrode as compared with the corresponding bare electrode in 0.2 mol/L phosphate buffer solution (pH 7.0) containing 3 × 10-9 mol/L luteolin and higher oxidation and reduction peak currents of luteolin at the modified electrode were observed. Further experiments demonstrated that oxidation peak current increased linearly with increasing luteolin concentration within the range from 1.0 × 10-10 to 1.6 × 10-8 mol/L with a detection limit of 3.2 × 10-11 mol/L and the range of spike recovery at four levels was between 98.7% and 103.6%. The method is simple, fast, sensitive and accurate, thereby providing an available approach for the determination of total flavonoids in Flos Ionicera.

Key words: Flos Ionicera, luteolin, ion liquid, modified electrode, total flavonoids, electrochemistry

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