摘要
目的建立同时测定和肝利胆颗粒中柚皮苷、新橙皮苷、黄芩苷3种黄酮类成分含量的高效液相色谱法。方法色谱柱为Agilent Zorbax SB C18柱(250 mm×4.6 mm,5μm),流动相为乙腈-0.2%磷酸溶液(20∶80,V/V),流速为1.0 m L/min,检测波长为283 nm,柱温为20℃,进样量为10μL。结果柚皮苷、新橙皮苷、黄芩苷的进样量分别在0.039 98~0.799 60μg,0.039 94~0.798 80μg,0.099 58~1.991 60μg范围内与峰面积线性关系良好(r≥0.999 5,n=6);精密度、重复性、稳定性试验的RSD均不超过2.0%(n=6);平均回收率分别为101.26%,98.74%,98.08%,RSD分别为1.21%,0.78%,1.26%(n=6)。结论该方法操作简便,结果准确,重复性好,可用于同时测定和肝利胆颗粒中柚皮苷、新橙皮苷、黄芩苷3种黄酮类成分的含量。
Objective To establish a high-performance liquid chromatography(HPLC)method for the simultaneous determination of three flavonoids(naringin,neohesperidin and baicalin)in Hegan Lidan Granules.Methods The chromatographic column was Agilent Zorbax SB C18 column(250 mm×4.6 mm,5μm),t he mobile phase was acetonitrile-0.2%phosphoric acid solution(20∶80,V/V),the flow rate was 1.0 mL/min,the detection wavelength was 283 nm,the column temperature was 20℃,and the injection volume was 10μL.Results The linear ranges of naringin,neohesperidin and baicalin were 0.03998-0.79960μg,0.03994-0.79880μg,0.09958-1.99160μg,respectively(r≥0.9995,n=6).The RSDs of precision,repeatability and stability tests were less than 2.0%(n=6).The average recoveries of naringin,neohesperidin and baicalin were 101.26%,98.74%,98.08%with RSDs of 1.21%,0.78%,1.26%(n=6),respectively.Conclusion The method is simple,accurate and reproducible,which can be used for the simultaneous determination of three flavonoids(naringin,neohesperidin and baicalin)in Hegan Lidan Granules.
作者
吴远波
吴克勤
刘宇政
王伟
吴靓
张鸿
WU Yuanbo;WU Keqin;LIU Yuzheng;WANG Wei;WU Jing;ZHANG Hong(Jiangxi Academy of Medical Science,Nanchang,Jiangxi,China 330006)
出处
《中国药业》
CAS
2021年第15期71-73,共3页
China Pharmaceuticals
基金
江西省青年科学基金资助项目[20192BAB215044]
江西省卫生计生委中医药科研课题[2018A313]
江西省教育厅科学技术研究项目[180166]。