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双黄连颗粒中绿原酸含量的HPLC测定
引用本文:张洪涛,蔡俊安,郭鑫慧. 双黄连颗粒中绿原酸含量的HPLC测定[J]. 中国中医药信息杂志, 2010, 17(4): 43-44
作者姓名:张洪涛  蔡俊安  郭鑫慧
作者单位:河南百年康鑫药业有限公司,河南,郸城,477150
摘    要:目的采用高效液相色谱法测定双黄连颗粒中绿原酸的含量。方法用外标一点法,Diamonsil ODS1 C18色谱柱,甲醇-水-冰醋酸(15:85:1)为流动相,流速为1.0mL/min,λ=324nm。结果绿原酸在0.060~1.210μg范围内呈良好线性,回归方程为Y=105427X+586.43,r2=0.9995,平均加样回收率为99.3%,RSD=0.82%(n=6)。结论本方法简便、准确,专属性强,测定结果重复性好,为双黄连颗粒中绿原酸的定量分析提供了科学有效的方法 。

关 键 词:双黄连颗粒  绿原酸  高效液相色谱法  含量测定

Determination of Chlorogenic Acid in Shuanghuanglian Keli by HPLC
ZHANG Hong-tao,CAI Jun-an,GUO Xin-hui. Determination of Chlorogenic Acid in Shuanghuanglian Keli by HPLC[J]. Chinese Journal of Information on Traditional Chinese Medicine, 2010, 17(4): 43-44
Authors:ZHANG Hong-tao  CAI Jun-an  GUO Xin-hui
Affiliation:(Henan Bainian Kangxin Pharmaceutical Co. Ltd, Dancheng 477150, China)
Abstract:Objective To establish the method for detemining the content of chlorogenic acid in Shuanghuanglian Keli by HPLC. Methods Using Diamonsil OD81 C18 column, with methanol-water-glacial acetic acid (15 : 85 : 1) as the mobile phase, detection wavelength as 324 nm and flow rate was 1.0 mL/min. Results The calibration curve was linear at the range of 0.060-1.210 μg for chlorogenic acid and the equation was Y= 105427X+586.43, r2=0.999 5. The average recovery was 99.3% and RSD was 0.82% (n =6). Conclusion This method was simple, accurate and proper, and the reduplication of the result was good, which provide scientific quantitative analysis method of chlorogenic acid in Shuanghuanglian Keli.
Keywords:Shuanghuanglian Keli  chlorogenic acid  HPLC  content determination
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