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茶叶科学 ›› 2010, Vol. 30 ›› Issue (6): 435-439.doi: 10.13305/j.cnki.jts.2010.06.005

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高效液相色谱-蒸发光散射检测法测定茶叶中单糖和双糖

袁勇, 黄建安, 李银花, 陈金华, 袁玲, 刘仲华*   

  1. 湖南农业大学茶学教育部重点实验室,国家植物功能成分利用工程技术研究中心,湖南 长沙 410128
  • 收稿日期:2010-03-19 修回日期:2010-05-06 发布日期:2019-09-11
  • 通讯作者: larkin-liu@163.com
  • 作者简介:袁勇(1982— ),男,湖南沅江人,硕士研究生,主要从事茶及植物功能成分化学研究。
  • 基金资助:
    湖南省重大科技专项“茯茶产业化关键技术研究与示范”(2008FJ1005),“十一五”农业部行业支撑计划“名优绿茶高效栽培加工关键技术研究”(NYHYZX07-021-12)

Determination of Monosaccharides and Disaccharides in Tea by High Performance Liquid Chromatography- Evaporative Light Scattering Detector

YUAN Yong, HUANG Jian-an, LI Yin-hua, CHEN Jin-hua, YUAN Ling, LIU Zhong-hua*   

  1. Key Lab of Tea Science of Ministry of Education, Hunan Agricultural University, National Research Center of Engineering & Technology for Utilization of Functional Ingredients from Botanical, Changsha 410128, China
  • Received:2010-03-19 Revised:2010-05-06 Published:2019-09-11

摘要: 建立了高效液相色谱-蒸发光散射检测器(HPLC-ELSD)测定茶叶中单糖和双糖的检测方法。采用Shodex NH2P-50-4E(4.6 mm×250 mm,5 μm)色谱柱,以水和乙腈为流动相进行梯度洗脱,梯度洗脱程序为:0~14 min,85%乙腈;14~16 min,85%~70%乙腈;16~28 min,70%乙腈;28~32 min,70%~85%乙腈,流速:1.0 mL/min,柱温:20℃,雾化管温度为30℃,漂移管温度为70℃,氮气压力为310.275 Pa。鼠李糖、阿拉伯糖、木糖、果糖、甘露糖、葡萄糖、蔗糖、麦芽糖在3.202~184.828 μg范围内程良好的线性关系,8种糖的加标回收率在90.97%~105.07%之间,最低检测限(S/N=3)范围在6.976~1376.297 ng。该方法具有操作简便,分离效果好等特点。

关键词: 高效液相色谱, 蒸发光散射检测器, 茶叶, 单糖, 双糖

Abstract: A method for determination of monosaccharide and disaccharide in tea by HPLC-ELSD was developed. Shodex NH2P-50-4E (4.6 mm×250 mm, 5 μm) column was used at 20℃, acetonitrile and water used as mobile phase, for gradient elusion with the flow rate of 1.0 mL/min. The ratio of organic solvent was controlled by a gradient elution procedure. The procedure was as follows: 85% acetonitrile in 0~14 min, 70%~80% acetonitrile 14~16 min, 70% acetonitrile 16~28 min, then 70%~80% acetonitrile 28~32 min. At last, the ratio of acetonitrile increased to 85%. With the use of evaporative light-scattering detector, the nebulization chamber temperature was 30℃, the drift tube temperature was 70℃ and nitrogen pressure was 310.275 Pa. The calibration curves of rhamnose, arabinose, xylose, fructose, mannose, glucose, sucrose and maltose showed good linearity in the range of 3.202~184.828 μg. The recoveries of fortified 8 kinds of sugar were 90.97%~105.07%, limit of detention was 6.976~1 376.297 ng. Results indicated that the method was simple, rapid and could effectively separate the target component.

Key words: HPLC, ELSD, tea, monosaccharides, disaccharides

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