目的:建立同时测定敷胸巴布贴中5种大黄蒽醌类成分(芦荟大黄素、大黄酸、大黄素、大黄酚、大黄素甲醚)含量的方法。方法:采用Agilent TC-C18(250 mm×4.6 mm,5μm)色谱柱,流动相甲醇-0.4%磷酸溶液(85:15),流速1.0 m L·min-1,柱温30℃,紫外检测波长254 nm。结果:5种蒽醌类成分之间有较好的分离度,芦荟大黄素线性范围0.094 2-0.942μg(r=0.9995),大黄酸线性范围0.036 9-0.369μg(r=0.9996),大黄素线性范围0.048 6-0.486μg(r=0.9999),大黄酚线性范围0.032 4-0.324μg(r=0.9998),大黄素甲醚线性范围0.069 6-0.696μg(r=0.9997),平均加样回收率分别为98.7%,98.3%,96.8%,96.8%,97.4%,RSD分别为0.7%,1.0%,2.1%,1.8%,2.4%。结论:该实验方法精确度高、重复性好,可用于敷胸巴布贴的质量控制。
Objective:To establish the method for simultaneous determination of five Rheum offieinale anthraquinones (including aloeemodin, rhein, emodin, chrysophanol, physcion) from Fuxiong Cataplasms. Methods:The analysis was achieved with an Agilent Zorbax TC -Ctsanalytical column(4.6 mm × 250 ram,5 μm) used with the column temperature 30 ℃. The detection wavelength for UV detector was 254 nm. The flow rate was set at 1.0 mL · min- 1 and mobile phase was consisted of methanol - 0.4% phosphoric acid( 85 : 15 ). Results : All the active constituents were well separated by this method. Linearities of aloe - emodin, rhein, emodin, chrysophanol and physcion were good in the ranges of 0.0942 - 0. 942 μg ( r = 0. 9995 ), 0. 0369 - 0. 369 μg ( r = 0. 9996) ,0. 0486 - 0. 486 μg( r = 0. 999 9) ,0.0324 - 0. 324 μg( r = 0. 999 8) ,0. 0696 - 0. 696 μg( r = 0.9997 ), respective- ly. The average recoveries of aloe - emodin, rhein, emodin, chrysophanol and physcion were 98.7 % ,98.3 % ,96.8 % ,96.8 % and 97.4% and RSD values were 0.7%, 1.0% ,2.1%, 1.8% ,2.4%. Conclusion:This method is accuracy and reproducibility. It can be effectively used for the quality control of Fuxiong Cataplasms.