摘要
目的建立测定麦冬药材中3个具有代表性的黄酮成分,甲基麦冬高黄酮A、麦冬甲基黄烷酮A和甲基麦冬二氢高异黄酮B的高效液相色谱法。方法采用HPLC-DAD,色谱柱为Comatex C18柱(4.6 mm×250 mm,5μm),流动相为乙腈-水(58∶42),流速1.0 m L·min-1,柱温30℃,检测波长296 nm,进样量20μL。结果甲基麦冬高黄酮A、麦冬甲基黄烷酮A和甲基麦冬二氢高异黄酮B 3种成分的线性方程分别为Y=493 321ρ+31 262(r=0.999 9)、Y=605 744ρ+40 941(r=0.999 9)、Y=586 672ρ+39 657(r=0.999 9);平均回收率分别为100.59%(RSD=1.51%)、99.27%(RSD=1.28%)、100.04%(RSD=1.33%)。结论建立的麦冬3种黄酮含量测定方法准确灵敏、重复性好,可应用于麦冬药材质量评价中。
OBJECTIVE To establish an HPLC method for simultaneous determination of methylophiopogonone A,methylophiopogonanone A,and methylophiopogonanone B. METHODS Comatex C18column( 4. 6 mm × 250 mm,5 μm) was used for the HPLC analysis. The mobile phase consisted of acetonitrile and water( 58∶ 42) and was eluted at the flow rate of 1 mL·min^- 1. The column temperature was maitained at 30 ℃. The detection wavelength was set at 280 nm. The injection volume was 15. 0 μL. RESULTS The linear regression equations of methylophiopogonone A, methylophiopogonanone A and methylophiopogonanone B were Y = 493 321ρ + 31 262( r = 0. 999 9),Y = 605 744ρ + 40 941( r = 0. 999 9),and Y = 586 672ρ + 39 657( r = 0. 999 9),respectively.The average recovery rates of the three flavones respectively were 100. 59%( RSD = 1. 51%),99. 27%( RSD = 1. 28%),and100. 04%( RSD = 1. 33%). CONCLUSION The established method for simultaneous determination of flavone constituents in Ophiopogonis Radix is accurate and sensitive,with good repeatability. It can be applied to the quality evaluation of Ophiopogonis Radix.
出处
《中国药学杂志》
CAS
CSCD
北大核心
2016年第8期655-658,共4页
Chinese Pharmaceutical Journal
基金
国家科技部“重大新药创制”资助项目(2014ZX09304307-002)
科技部科技惠民资助项目(2013GS510102)
四川省中医管理局资助项目(2014F038)
四川省科技厅科技支撑重点资助项目(2015SZ0033)