摘要
目的:建立一种超高效液相色谱法同时测定丹蛭降糖胶囊中丹皮酚、芍药苷的含量。方法:色谱柱为Waters Acquity UPLC BEH C18(50 mm×2.1 mm,1.7μm)柱,以乙腈-0.1%磷酸为流动相进行梯度洗脱,流速为0.25 mL.min-1,柱温为30℃,检测波长为230 nm。结果:丹皮酚和芍药苷的线性范围分别为0.653~1.959μg(r=0.999 7)和0.108~0.324μg(r=0.999 9),平均加样回收率分别为99.46%,RSD=0.46%(n=6)和99.19%,RSD=0.49%(n=6)。结论:新建方法简便、快速、准确、易行,可用于控制制剂质量。
Objective: To establish a UPLC method for the simultaneous determination of paeonol and paeoniflorin in Danzhi Jiangtang capsule.Methods: Separation was performed on Waters Acquity UPLC BEH C18(50 mm×2.1 mm,1.7 μm) column by a gradient elution using acetonitrile and 0.1% phosphoric acid aqueous solution as the mobile phase at a flow rate of 0.25 mL·min-1 and a column temperature of 30 ℃.The detection wave length was 230 nm.Results: The linearities of paeonol and paeoniflorin were in the range of 0.653~1.959 μg(r=0.999 7) and 0.108~0.324 μg(r=0.999 9);average recoveries were 99.46%,RSD=0.46%(n=6),99.19%,RSD=0.49%(n=6),respectively.Conclusion: The method is accurate,sensitive,reproducible,and suitable for the quality control of Danzhi Jiangtang capsule.
出处
《中国新药杂志》
CAS
CSCD
北大核心
2012年第12期1337-1340,共4页
Chinese Journal of New Drugs
基金
国家"重大新药创制"科技重大专项(2010ZX09102-209)
安徽省中医药管理局课题(2009ZY03)