摘要
目的建立一种同时测定黄连解毒汤中7种活性成分(栀子苷、黄芩苷、盐酸巴马汀、盐酸小檗碱、汉黄芩苷、黄芩素和汉黄芩素)含量的RP-HPLC方法。方法采用迪马Diamonsil C18色谱柱(250×4.6 mm,5μm),以乙腈(A)-0.05%磷酸二氢钾和0.05%三乙醇胺(用磷酸调pH到3.0)(B)为流动相,梯度洗脱:0～9 min,84%B;9～27 min,84%→73%B;27～35 min,73%→70%B;35～39 min,70%→68%B;39～42 min,68%→60%B;42～46 min,60%→52%B;46～53 min,52%→45%B;53～60 min,45%→84%B。流速0.8 ml/min,检测波长254 nm,柱温35℃。结果在60 min内黄连解毒汤中栀子苷、黄芩苷、盐酸巴马汀、盐酸小檗碱、汉黄芩苷、黄芩素和汉黄芩素7种成分被完全分离;回归方程显示7种成分的峰面积与其浓度呈良好的线性相关;7种成分的加样回收率(n=6)为94.92%～106.76%,RSD均小于2.0%。结论利用反相高效液相色谱法,建立了一种简便准确,可同时测定黄连解毒汤中7种活性成分含量的检测方法。
Objective To establish a method of RP-HPLC which can simultaneously detect the contents of seven active components including geniposide,baicalin,palmatine,berberine,wogonoside,baicalein and wogonin in Huanglian Jiedu decoction.Methods The samples were separated by a Diamonsil C18 column（250×4.6 mm,5 μm） with a linear gradient elution under predetermined procedures（0～9 min,84% B;9～27 min,84%→73% B;27～35 min,73%→70% B;35～39 min,70%→68% B;39～42 min,68%→60% B;42～46 min,60%→52% B;46～53 min,52%→45% B;53～60 min,45%→84% B）.Additionally,acetonitrile（A） and 0.05% potassium dihydrogen phosphate mixtured with 0.05% triethanolamine（PH was regulated to 3.0 by phosphoric acid）（B）were used as mobile phase at a flow rate of 0.8 mL·min-1.The column temperature was set at 35 ℃.The eluate was detected at the wavelength of 254 nm.Results Seven active components mentioned above in Huanglian Jiedu decoction were completely separated within 60 minutes by the method of RP-HPLC.The regression model suggested a sound linear correlation between the peak areas of seven components and corresponding contents.And the recovery rate（n=6） of the markers listed above ranged from 94.92% to 106.76%.All the relative standard deviations（RSDs） were less than 2.0%.Conclusion The method of RP-HPLC was convenient and accurate to detect the contents of seven active components in Huanglian Jiedu decoction simultaneously.
出处
《浙江预防医学》
2011年第11期15-19,共5页
Zhejiang Journal of Preventive Medicine
基金
浙江省教育厅科研项目(Y200909752)
浙江省中医药科研项目(2011ZA018)
