摘要
目的建立同时测定加味香连丸中芍药苷、柚皮苷、橙皮苷和黄芩苷的HPLC法。方法采用Hypersil ODS色谱柱(4.6 mm×200 mm,5μm);乙腈-0.2%磷酸水溶液为流动相;体积流量1.0 m L/min;检测波长274 nm;柱温为25℃。结果加味香连丸中的芍药苷、柚皮苷、橙皮苷和黄芩苷分别在0.32~7.68μg/m L(r=0.999 8)、2.08~49.92μg/m L(r=0.999 8)、0.68~16.32μg/m L(r=0.999 7)和1.32~31.68μg/m L(r=0.999 8)范围内与峰面积呈良好的线性关系;平均回收率分别为98.2%(RSD为0.88%)、97.7%(RSD为1.3%)、98.7%(RSD为0.94%)和97.9%(RSD为0.90%)。结论本方法适用于加味香连丸中4种成分的定量测定。
AIM To establish an HPLC method for simultaneous determination of paeoniflorin,naringin,hesperidin and baicalin in Jiawei Xianglian Pills. METHODS Using Hypersil ODS column( 4. 6 mm × 200 mm,5μm),mobile phase was acetonitrile-0. 2% phosphoric acid solution with a flow rate of 1. 0 m L /min,the detection wavelength was 274 nm,and the column temperature was 25 ℃. RESULTS The calibration curves were linear in the ranges of 0. 32- 7. 68 μg / m L( r = 0. 999 8) for paeoniflorin,2. 08- 49. 92 μg / m L( r = 0. 999 7) for naringin,0. 68- 16. 32 μg / m L( r = 0. 999 5) for hespiridin and 1. 32- 31. 68 μg / m L( r = 0. 999 7) for baicalin,the average recoveries of these chemical constituents were 98. 2%( RSD = 0. 88%),97. 7%( RSD = 1. 3%),98. 7%( RSD = 0. 94%) and 97. 9%( RSD = 0. 90%),respectively. CONCLUSION This method is applicable for the determination of these four constituents in Jiawei Xianglian Pills.
出处
《中成药》
CAS
CSCD
北大核心
2015年第9期1955-1958,共4页
Chinese Traditional Patent Medicine
基金
辽宁医学院横向课题(LYHX2013001)