摘要
目的:建立六味能消胶囊中木香烃内酯、去氢木香烃内酯、大黄素、大黄酚4个成分含量测定的方法。方法:采用Atlantis C18色谱柱(150 mm×4.6 mm,5μm),以甲醇-0.1%磷酸水为流动相,梯度洗脱,检测波长225 nm(0~25 min检测木香烃内酯、去氢木香烃内酯)、254 nm(25~40 min检测大黄素、大黄酚),柱温25℃。结果:木香烃内酯、去氢木香烃内酯、大黄素、大黄酚的线性范围分别为0.665 6~33.28、0.563 7~31.84、0.524 8~26.24、0.585 6~29.28μg·mL^-1;平均回收率(n=6)分别为99.28%(RSD=1.8%),101.7%(RSD=1.6%),101.2%(RSD=2.0%),99.36%(RSD=1.8%)。5批样品中木香烃内酯、去氢木香烃内酯、大黄素、大黄酚含量分别为2.32~2.41、2.48~2.62、0.42~0.48、1.26~1.33 mg·g^-1。结论:该方法可用于六味能消胶囊中木香烃内酯、去氢木香烃内酯、大黄素、大黄酚的同时测定。
Objective: To develop an HPLC method for the determination of costunolide,dehydrocostus lactone,emodin,and chrysophanol in Liuweinengxiao capsules. Methods: Samples were analyzed on an Atlantis C18column( 150 mm × 4. 6 mm,5 μm) eluted with methanol and water containing 0. 1 % phosphate acid as mobile phases in a linear gradient mode. The flow rate was kept at 1. 0 m L·min^-1,and the column temperature was set at 25 ℃. The detector wavelengths were 225 nm( 0-25 min) for costunolide and dehydrocostus lactone,254 nm( 25-40 min) for emodin and chrysophanol. Results: The linear ranges of costunolide,dehydrocostus lactone,emodin and chrysophanol were 0. 665 6-33. 28 μg·mL^-1,0. 563 7-31. 84 μg·mL^-1,0. 524 8-26. 24 μg·mL^-1,0. 585 6-29. 28 μg·mL^-1,respectively. The average recoveries( n = 6) of the four constituents were 99. 28 %( RSD = 1. 8 %),101. 7 %( RSD = 1. 6 %),101. 2 %( RSD = 2. 0 %),99. 36 %( RSD = 1. 8%),respectively. The contents of the four constituents were 2. 32-2. 41 mg·g^-1,2. 48-2. 62mg·g^-1,0. 42-0. 48 mg·g^-1,and 1. 26-1. 33 mg·g^-1. Conclusion: The established method can be used for simultaneous determination of costunolide,dehydrocostus lactone,emodin and chrysophanol in Liuweinengxiao capsules.
出处
《药物分析杂志》
CAS
CSCD
北大核心
2015年第2期241-245,共5页
Chinese Journal of Pharmaceutical Analysis