摘要
目的建立金莲花药材中3种碳苷黄酮含量同时测定的方法,以比较不同产地金莲花药材及不同部位中3种成分的含量。方法采用RP-HPLC法。色谱柱:Shim-pack C18柱(250 mm×4.6 mm,5μm),流动相:乙腈体积分数为0.35%的磷酸溶液(体积比为16∶84),流速:1.0 mL·min-1,检测波长:345 nm,柱温:25℃。结果荭草苷、牡荆苷、荭草素-2″-O-β-L-半乳糖苷能够达到基线分离;荭草苷在9.94~99.40 mg·L-1、牡荆苷在2.49~24.90 mg·L-1、荭草素2″OβL半乳糖苷在10.64~106.40 mg·L-1内线性关系良好。结论本方法为金莲花药材的综合利用和资源开发提供了参考,有利于控制金莲花药材的质量。
Objective To establish a high performance liquid chromatographic method for analysis of three flavonoid C-glycosides from different habitats and different parts of TroUius chinensis. Methods Shim-pack C18 column(250 mm x 4.6 mm,5 μm)was used with a mixture of acetonitrile-0. 35% phosphoric acid( V: V = 16:84 ) as the mobile phase. The flow rate was 1.0 mL. rain - 1, detection wavelength was set at 345 nm, column temperature was set at 25 ℃. Results The linear range of orientin, vetixin and 2"-O-β-L-galactopyranosyl orientin were 9.94-99.40,2. 49-24.90 and 10. 64- 106. 40 mg.L-1 ,respectively. Conclusions The method is simple, accurate and sensitive with good reproducibility. It can provide references for quality control and resources development of the medicinal materials.
出处
《沈阳药科大学学报》
CAS
CSCD
北大核心
2013年第3期197-200,共4页
Journal of Shenyang Pharmaceutical University