摘要
目的:建立HPLC法测定仙蟾胶囊中华蟾酥毒基及脂蟾毒配基含量。方法:采用高效液相色谱法,色谱柱为Agilent ZORBAXSB-C18(250mm×4.6mm,5μm),流动相为乙腈(A)-水(B),梯度洗脱,流速1.0mL.min-1,检测波长296nm,柱温40℃。结果:华蟾酥毒基及脂蟾毒配基分别在4.0~100.0μg.mL-1(r=0.9999)及2.0~100.2μg.mL-1(r=0.9999)范围内线性关系良好,平均回收率(n=6)分别为101.6%(RSD=1.5%)和97.65%(RSD=1.6%)。结论:本法操作简便、准确,重复性好,可用于仙蟾胶囊的质量控制。
Objective:To develop an HPLC method for the determination of cinobufagin and resibufogenin in Xianchan capsules.Methods:The chromatographic separation was achieved on an Agilent ZORBAX SB-C18(250 mm×4.6 mm,5 μm) column;The mobile phase was acetonitrile(A)-water(B) with gradient elution at the flow rate of 1.0 mL·min-1.The wavelength was 296 nm and the column temperature was 40 ℃.Results:The calibration curves were linear in the ranges of 4.0-100.0 μg·mL-1(r=0.9999) for cinobufagin and 2.0-100.2 μg·mL-1(r=0.9999) for resibufogenin.The recoveries(n=6) of cinobufagin and resibufogenin were 101.6%(RSD=1.5%) and 97.65%(RSD=1.6%).Conclusion:The method is simple and accurate with good reproducibility,and can be used for the quality control of Xianchan capsules.
出处
《药物分析杂志》
CAS
CSCD
北大核心
2010年第10期1845-1848,共4页
Chinese Journal of Pharmaceutical Analysis