摘要
目的:建立高效液相色谱方法同时测定山腊梅清感茶中4种黄酮苷含量的方法。方法:采用依利特hypersil ODS2色谱柱(4.6 mm×250 mm,5μm),以乙腈-0.1%冰醋酸为流动相进行梯度洗脱,流速1.0 m L·min^-1,检测波长344 nm,柱温35℃。结果:芦丁在7.012~70.12 mg·L^-1线性关系良好(r=0.999 6),平均回收率为100.68%,RSD 3.3%,山柰酚-3-O-β-D-半乳糖-(6-1)-α-L-鼠李糖苷在5.126~51.26 mg·L^-1线性关系良好(r=0.999 9),平均回收率为98.48%,RSD 1.7%,山柰酚-3-O-芸香糖苷在2.631~26.31 mg·L^-1线性关系良好(r=0.999 8),平均回收率为101.82%,RSD 1.9%,紫云英苷在2.634~26.34 mg·L^-1线性关系良好(r=0.999 9),平均回收率为97.02%,RSD 1.7%。结论:该方法操作简便,准确,重复性好,可用于山腊梅清感茶的质量控制。
Objective: The aim of this study was to establish an HPLC method for simultaneous determination of the content of four flavonoid glycosides in Shanlamei Qinggan Cha. Method: Using an Elite hypersil ODS2 column (4.6 mm× 250 mm, 5 μm) , the mobile phase was aeetonitrile-0.1% acetic acid, with flow rate of 1.0 mL·min^-1 The detective wavelength was at 344 nm and the column temperature was 35 ℃. Result: The standard curve presented a linear range from 7. 012-70. 12 mg·L^-1 for rutin (r = 0. 999 6) , the average recovery was 100.68% with RSD of 3.27%. The calibration curve was linear in the range of 5. 126-51.26 rag-L-l for kaempferol-3-O-β-D-galactose-(6-1 )-a-L-rhamnoside (r = 0.999 9), the average recovery was 98.48% with RSD of 1.7%. The calibration curve was linear in the range of 2. 631-26.31 mg ·L^-1 for kaempferol- 3-O-rutinoside (r = 0. 999 8), the average recovery was 101.82% with RSD of 1.9%. The standard curve presented a linear range from 2. 634-26.34 mg· L^-1 for astragalin ( r = 0. 999 9) , the average recovery was 97.02% with RSD of 1.7%. Conclusion: The method was fast, accurate and simple in good reproducibility, which could be used to control the quality of Shanlamei Qinggan Cha.
出处
《中国实验方剂学杂志》
CAS
北大核心
2014年第24期64-66,共3页
Chinese Journal of Experimental Traditional Medical Formulae
基金
江西省教育厅项目(12750)