摘要
目的:建立同时测定补阳还五汤中芍药苷、毛蕊异黄酮苷、阿魏酸含量的方法。方法:采用反相高效液相色谱法。色谱柱为OdyssilC18(250mm×4.6mm,5μm),流动相为乙腈-水-0.1%磷酸(16:64:20,V/V/V),检测波长为230nm(芍药苷)、260nm(毛蕊异黄酮苷)、328nm(阿魏酸),流速为1.0ml/min,柱温为30℃。结果:芍药苷、毛蕊异黄酮苷、阿魏酸的进样量分别在0.0964~0.9640μg(r=0.9992)、0.0990~0.9900μg(r=0.9996)、0.00836~0.0836μg(r=0.9994)范围内与各自峰面积积分值呈良好线性关系;三者的平均加样回收率分别为99.72%、99.14%和97.96%,RSD分别为0.5%、1.1%和1.4%(n均为6)。结论:本方法简便、快速、灵敏度高、重复性好,适用于补阳还五汤的质量控制。
OBJECTIVE:To establish the method for simultaneous determination of paeoniflorin,calycosin and ferulic acid in Buyang huanwu decoction.METHODS:RP-HPLC method was adopted.The determination was performed on Odyssil C 18(250 mm× 4.6 mm,5 μm)column with mobile phase consisted of acetonitrile-water-0.1% phosphate acid(16:64:20,V/V/V)at the flow rate of 1.0 ml/min.The detection wavelength was set at 230 nm(paeoniflorin),260 nm(calycosin)and 328 nm(ferulic acid).The column temperature was 30 ℃.RESULTS:The linear ranges were 0.096 4-0.964 0 μg(r=0.999 2)for paeoniflorin,0.099 0-0.990 0 μg for calycosin(r=0.999 6)and 0.008 36-0.083 6 μg for ferulic acid(r=0.999 4),respectively.The average recoveries were 99.72% for paeoniflorin(RSD=0.5%,n=6),99.14% for campanulin(RSD=1.1%,n=6)and 97.96% for ferulic acid(RSD=1.4%,n= 6).CONCLUSION:The method is simple,quick,sensitive and reproducible for the quality control of Buyang huanwu decoction.
出处
《中国药房》
CAS
CSCD
2013年第3期232-234,共3页
China Pharmacy
基金
国家自然科学基金资助项目(No.30873221
No.81173175)
湖南省自然科学基金项目(No.10JJ2023)