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机构地区:[1]益阳市中医院,湖南益阳413000 [2]南华大学,湖南衡阳421001
出 处:《中成药》2014年第6期1199-1202,共4页Chinese Traditional Patent Medicine
摘 要:目的建立同时测定妇炎净片(苦玄参、当归、五指毛桃等)中苦玄参苷IA、阿魏酸、补骨脂素和异补骨脂素4种成分的高效液相色谱测定方法。方法采用KromasilC18色谱柱(5μm,4.6mm×250mm),以1%冰乙酸-乙腈为流动相进行梯度洗脱,体积流量1.0mL/min,检测波长245nm。结果苦玄参苷IA、阿魏酸、补骨脂素和异补骨脂素分别在15~150μg/mL、2.5—25μg/mL、1.0~10μg/mL、1.2~12μg/mL范围内线性良好,r值均大于0.999,平均加样回收率分别为99.3%、98.8%、99.0%和99.2%,相对标准偏差(RSD)均小于0.7%(n=9)。结论该方法简便,结果准确,可有效地用于妇炎净片的质量控制。AIM To establish HPLC method for determining four constituents (picfeharraenin IA, ferulic acid, psoralen and isopsoralen ) in Fuyanjing Tablets (Picriae Herba, Angelicae sinensis Radix, Fici simplicissmae Radix, etc. ). METHODS HPLC was performed on Kromasil C18 (5 μm, 4. 6 mm ×250 mm) column with the mobile phase of 1% acetic acid solution as phase A and acetonitrile as phase B in gradient elution manner. The de- tection wavelength was set at 245 nm. RESULTS The calibration curve was linear over the concentration range of 15 - 150μg/mL for picfeltarraenin IA, 2. 5 - 25μg/mL for ferulic acid, and 1.0 ~10 μg/mL for psoralen, and 1.2 - 12 μg/mL for isopsoralen , respectively. The correlation coefficient of all curves was more than 0. 999. The average recoveries of four constituents were 99.3% for picfeltarraenin IA, 98.8% for ferulic acid, 99.0% for psoralen, and 99.2% for isopsoralen, and the RSD value of precision was less than 0. 7% ( n = 9), respectively. CONCLUSION The developed HPLC method could be used for the quality control of Fuyanjing Tablets.
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