程智勇, 韩凤梅, 蔡敏, 陈勇. HPCE法测定双黄连口服液中的黄芩苷和绿原酸J. 药学学报, 1999, 34(11): 854-857.
引用本文: 程智勇, 韩凤梅, 蔡敏, 陈勇. HPCE法测定双黄连口服液中的黄芩苷和绿原酸J. 药学学报, 1999, 34(11): 854-857.
Cheng Zhiyong, Han Fengmei, Cai Min , Chen Yong, . SEPARATION AND QUANTITATIVE DETERMINATION OF BAICALIN AND CHLOROGENIC ACID IN SHUANGHUANGLIAN ORAL LIQUID BY HIGH PERFORMANCE CAPILLARY ELECTROPHORESISJ. Acta Pharmaceutica Sinica, 1999, 34(11): 854-857.
Citation: Cheng Zhiyong, Han Fengmei, Cai Min , Chen Yong, . SEPARATION AND QUANTITATIVE DETERMINATION OF BAICALIN AND CHLOROGENIC ACID IN SHUANGHUANGLIAN ORAL LIQUID BY HIGH PERFORMANCE CAPILLARY ELECTROPHORESISJ. Acta Pharmaceutica Sinica, 1999, 34(11): 854-857.

HPCE法测定双黄连口服液中的黄芩苷和绿原酸

SEPARATION AND QUANTITATIVE DETERMINATION OF BAICALIN AND CHLOROGENIC ACID IN SHUANGHUANGLIAN ORAL LIQUID BY HIGH PERFORMANCE CAPILLARY ELECTROPHORESIS

  • 摘要: 目的:建立双黄连口服液中黄芩苷和绿原酸含量测定的毛细管电泳法。方法:用毛细管区带电泳和紫外检测模式测定双黄连口服液中黄芩苷和绿原酸的含量,电泳条件:以40 m mol·L-1 硼砂为电泳介质( 测定黄芩苷和绿原酸的pH值分别为9-00 和9-55) ,未涂层弹性融硅毛细管(50 μm ×39-5 cm ,有效分离长度34-8 cm) 为分离通道,压力进样(68-95 kPa·s),17 kV恒压电泳(25 ℃) ,黄芩苷和绿原酸的检测波长分别为285 ,326 nm 。结果:在20~640μg·mL-1 和8 ~400 μg·mL-1 范围内,黄芩苷和绿原酸可分别进行定量分析,二者加样回收率分别为100-60 % ±2-36 % 和99-68% ±2-27 % 。结论:本方法简便、快速,结果准确,重现性好,可用于双黄连口服液的质量控制。

     

    Abstract: AIM: To establish a high performance capillary electrophoresis (HPCE) method for the separation and quantitative determination of baicalin and chlorogenic acid in Shuanghuanglian oral liquid. METHODS: Based on the mode of capillary zone electrophoresis, baicalin and chlorogenic acid were separated successfully from other components and determined within 14 minutes under the optimum electrophoretic conditions as follows:uncoated fused silica capillary (34 8 cm×39 5 cm, 50 μm ID), 40 mmol·L-1 borax (pH 9.00 for baicalin and pH 9.55 for chlorogenic acid), applied voltage 17 kV, UV 285 nm for baicalin and 326 nm for chlorogenic acid, pressure injection 68 95 kPa·s. RESULTS: The relative peak areas of the analytes increase linearly with the increase of their concentrations in the range of 20~640 μg·mL-1 for baicalin and 8~400 μg·mL-1 for chlorogenic acid. Their recoveries are 100.60%±2.36% and 99.68%±2.27% respectively. CONCLUSION: The analytical results demonstrate that the method is convenient, rapid and well reproducible, and can be used as a reliable tool for the quality control of this prescription.

     

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