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作 者:杨静[1] 杨志福[1] 陈敏纯[1] 奚苗苗[1] 田云[1] 贾艳艳[1] 文爱东[1]
机构地区:[1]第四军医大学西京医院药剂科,西安710032
出 处:《中国药学杂志》2010年第4期248-251,共4页Chinese Pharmaceutical Journal
基 金:国家自然科学基金资助项目(30672662)
摘 要:目的比较红花当归单煎共煎液中有效成分羟基红花黄色素A和阿魏酸含量的变化,初步探索2味中药配伍的变化规律。方法采用RP—HPLC,色谱柱为Shim—packVP—ODSC18(4.6mm×150mm,5μm),流动相为甲醇-0.02mol·L^-1磷酸二氢钾缓冲液(磷酸调节pH至3.5),采用梯度洗脱进行分析;检测波长为230nm,流速为1.0mL·min^-1。结果羟基红花黄色素A回归方程Y=22821ρ-4105.1,r=0.9999,在2.5—50mg·L^-1内线性相关良好,平均加样回收率为100.1%,RSD为2.2%;阿魏酸回归方程Y:70219ρ-2573.9,r=0.9999,在0.5~10mg·L^-1内线性相关良好,平均加样回收率为101.4%,RSD为3.0%。结论红花当归共煎液中羟基红花黄色素A和阿魏酸含量比各单煎液中含量高。共煎更有助于有效成分的提取。本方法简便、快速、准确,适用于同时测定羟基红花黄色素A和阿魏酸的含量。OBJECTIVE To compare the content variation of hydroxysafflor yellow A and ferulic acid between single and mixed decoction of Safflower and Angelica. METHODS A RP-HPLC was performed on a Shim-pack VP-ODS C18 column(4.6 mm × 150 mm, 5 μm)with a gradient elution system composed of methanol and 0. 02 mol · L ^-1 potassium dihydrogen phosphate solutions ( adjusted to pH 3.0 with phosphoric acid). The wavelength of UV detection was set at 230 nm. The flow rate was 1.0 mL · min^-1. RESULTS The calibration curve of hydroxysafflor yellow A was linear within the range of 2.5 - 50 mg ·L ^-1 ( Y = 22 82 1ρ - 4 105. 1, r =0. 999 9). The mean absolute recovery was 100. 1% and RSD was 2. 2%. The curve of ferulic acid was linear within the range of 0. 5 - 10 mg · L^-1 ( Y =70 219ρ -2 573.9 ,r =0. 999 9). The mean absolute recovery was 101.4% and RSD was 3.0%. CONCLUSION The content of hydroxysafflor yellow A and ferulic acid in mixed decoction is higher than the single decoction of Safflower and Angelica. The mixed decoction is favorable for the extraction of hydroxysafflor yellow A and ferulic acid. The method is convenient, rapid, accurate and successfully applied to detect hydroxysafflor yellow A and fendic acid simultaneously.
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