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非水毛细管电泳法测定藤黄中藤黄酸的含量
引用本文:欧婉露,李玉娟,石冬冬,屈锋.非水毛细管电泳法测定藤黄中藤黄酸的含量[J].色谱,2015,33(2):152-157.
作者姓名:欧婉露  李玉娟  石冬冬  屈锋
作者单位:1. 北京理工大学生命学院, 北京 100081; 2. 中国农业科学院饲料研究所, 北京 100081
基金项目:国家重点基础研究发展计划项目(“973”项目)(2012CB910603);国家自然科学基金项目(21175011,21375008,81202996)
摘    要:藤黄酸(gambogic acid, GA)等环氧杂蒽酮类化合物的水溶性差,可通过非水毛细管电泳(non-aqueous capillary electrophoresis, NACE)分析。本文系统地考察了添加20%~60%(v/v)的甲醇或乙腈的运行电解质溶液对藤黄提取液中藤黄酸分离的影响。比较了不同的运行电解质溶液、运行电解质溶液浓度、pH、添加剂 β-环糊精的浓度、分离温度及分离电压的影响,建立了测定藤黄药材中藤黄酸含量的非水毛细管电泳方法。在40%乙腈、10 mmol/L β-环糊精、20 mmol/L四硼酸钠(pH 9.86)为运行电解质溶液、分离电压为10 kV、分离温度为30 ℃、检测波长为280 nm的条件下进行测定。结果表明,藤黄酸在2~2000 mg/L范围内线性关系良好,相关系数为0.9996,检出限(S/N=3)为2 mg/L。将本方法应用于越南、泰国、缅甸、印度4个产地的藤黄药材中藤黄酸的含量测定,测得含量为1.67~472.40 mg/g(相对标准偏差(RSD)为1.12%~2.60%),其中越南产藤黄中藤黄酸含量低,其他产地藤黄中藤黄酸的含量高。实际藤黄样品中藤黄酸的加标回收率为95.2%~105.6%。非水毛细管电泳方法简单、快速、重现性好,可用于藤黄药材中藤黄酸的含量测定。

关 键 词:非水毛细管电泳  藤黄  藤黄酸  
收稿时间:2014-11-05

Determination of gambogic acid in Gamboge by non-aqueous capillary electrophoresis
OU Wanlu;LI Yujuan;SHI Dongdong;QU Feng.Determination of gambogic acid in Gamboge by non-aqueous capillary electrophoresis[J].Chinese Journal of Chromatography,2015,33(2):152-157.
Authors:OU Wanlu;LI Yujuan;SHI Dongdong;QU Feng
Institution:1. School of Life Science, Beijing Institute of Technology, Beijing 100081, China; 2. Feed Research Institute, Chinese Academy of Agricultural Sciences, Beijing 100081, China
Abstract:Gambogic acid (GA), a kind of caged xanthones, has low solubility in water. A non-aqueous capillary electrophoresis (NACE) was established for the determination of GA in Gamboge based on the optimized conditions. The effect of 20%-60% methanol or acetonitrile spiked in running solution was investigated. The effects of compositions, concentration, pH, additives like β-cyclodextrin in running buffer were thoroughly studied. Applied voltage and applied temperature were also observed. Optimal electrophoretic conditions were as follows: 20 mmol/L sodium borohydride solution (pH 9.86) containing 40% (v/v) acetonitrile, 10 mmol/L β-cyclodextrin as running buffer, applied voltage of 10 kV, capillary temperature of 30 ℃ and detection wavelength of 280 nm. The calibration curve had good linearity in the range of 2-2000 mg/L with the correlation coefficient of 0.9996. The limit of quantification (S/N=3) of the method was 2 mg/L. The quantifications of GA in Gamboge from different producing places including Vietnam, Thailand, Burma, India were 1.67-472.40 mg/g with the RSD (n=3) of 1.12%-2.60%. The content of Gamboge from Vietnam is obviously low while the others are high. The recoveries of GA spiked in real samples ranged from 95.2% to 105.6%. The method of NACE is simple, efficient and of good reproducibility, can be served as a novel reference to identify and control the quality of Gamboge.
Keywords:Gamboge  gambogic acid  non-aqueous capillary electrophoresis (NACE)  
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