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作 者:申涛[1] 徐海燕[2] 姜煜[1] 栾爽[1] 赵怀清[1]
机构地区:[1]沈阳药科大学药学院,辽宁沈阳110016 [2]沈阳药科大学高等职业技术学院,辽宁沈阳110026
出 处:《沈阳药科大学学报》2008年第8期642-645,共4页Journal of Shenyang Pharmaceutical University
摘 要:目的建立同时测定畅鼻通颗粒中桂皮酸、黄芩苷和黄芩素含量的反相高效液相色谱法。方法采用反相高效液相色谱法进行含量测定。色谱柱为Diamonsil^TM C18(4.6mm×200mm,5μm)色谱柱,流动相为甲醇-乙腈-体积分数为1%的冰醋酸水溶液(体积比为65:20:115),流速为1.0mL·min^-1,检测波长为280nm。结果桂皮酸在0.82~8.20mg·L^-1内,黄芩苷在31.00~310.00mg·L^-1内,黄芩素在3.20--32.00mg·L^-1内,质量浓度与峰面积线性关系良好,相关系数分别为0.9999、0.9999和0.9997;平均回收率分别为101.1%、100.5%和101.4%;精密度RSD均小于2.0%。结论RP-HPLC法可用于畅鼻通颗粒的质量控制。Objective To develop an RP-HPLC method to determine simultaneously the concentrations of cinnamic acid, baicalin and baicalein in Changbitong (traditiona Chinese medicines) granules. Methods The separation was performed on a DiamonsilTM C18 (4.6 mm × 200 mm, 5 μm) column with a mixture of methanol-acetonitrile-1% acetic acid solution (V: V: V = 65:20:115) as mobile phase. The flow rate was 1.0 mL· min^-1 and the detection wavelength was set at 280nm. Results A good linearity was obtained within the range of 0.82 - 8.20 mg· L^-1 ( r = 0. 999 9) for cinnamic acid, 31.00 - 310.00 mg·L^-1 ( r = 0. 999 9)for baicalin and 3.20- 32.00 mg· L^-1( r = 0. 999 7) for baicalein. The average recoveries of the three components were 101.1%, 100.5 % and 101.4 %, respectively. The precision was not more than 2.0 %. Conclusions The method is proved to be selective and reproducible; it is suitable for the quality control of Changbitong granules.
关 键 词:畅鼻通颗粒 桂皮酸 黄芩苷 黄芩素 高效液相色谱法
分 类 号:R917[医药卫生—药物分析学]
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