摘要
目的建立测定丹酚及其滴丸中6种主要丹酚酸含量的方法。方法采用HPLC法,Unitary C18色谱柱,乙腈-0.05%磷酸水为流动相梯度洗脱,检测波长286 nm,流速为1.1 ml·min^-1,柱温为35℃。结果该色谱条件下,6种酚酸类成分可完全分离。丹参素、原儿茶醛、迷迭香酸、紫草酸、丹酚酸B和丹酚酸A的线性范围分别为2.07~20.66μg·mL^-1(r=0.9998)、2.53~25.30μg·mL^-1(r=0.9999)、8.12~40.60μg·mL^-1(r=0.9999)、11.24~56.20μg·mL^-1(r=0.9999)、99.60~996.00μg·mL^-1(r=0.9999)、1.00~10.02μg·mL^-1(r=0.9998),6种成分的平均回收率为99.24%~101.55%,RSD均小于2%。结论该测定方法准确度高,重复性好,专属性强,可同时测定丹酚及其滴丸中6种丹酚酸的含量。
Objective To establish a method for determining six main phenolic acids in extracts of Salvia miltiorrhiza. Methods Unitary C18 column was used with acetonitrile-0. 05% H3PO4 water at a dectection wave-length of 286 nm. The flow rate was 1. 1 ml·min^- 1and the column temperature was 35 ℃. Results Linearity was obtained over the range of 2. 07- 20. 66 μg·mL^-1( r =0. 9998) for Danshensu,2. 53-25. 30 μg·mL^-1( r =0. 9999) for portoeaetehualdehdye,8. 12- 40. 60 μg·mL^-1( r =0. 9999) for rosmarinic acid,11. 24-56. 20 μg·mL^-1( r = 0. 9999)for lithospermic acid,99. 60- 996. 00 μg·mL^-1( r = 0. 9999) for salvianolic acid B,1. 00- 10. 02 μg·mL^-1( r =0. 9998) for salvianolic acid A. The average recovery of six phenolic acids ranged from 99. 31% to 101. 16%,RSD ﹤2%. Conclusion This method is accurate,reproducible and specific,which can be used to determine six main phenolic acids in water extracts of salvia miltiorrhiza and its dropping pills simultaneously.
出处
《解放军药学学报》
CAS
CSCD
2016年第2期155-158,共4页
Pharmaceutical Journal of Chinese People's Liberation Army
关键词
HPLC
丹参素
原儿茶醛
迷迭香酸
紫草酸
丹酚酸B
丹酚酸A
HPLC
Danshensu
portoeaetehualdehdye
rosmarinic acid
lithospermic acid
salvianolic acid B
salvianolic acid A