摘要
目的:建立HPLC同时测定天佛参口服液中华蟾酥毒基和脂蟾毒配基的含量。方法:采用Waters SymmetryShield^TM RP18色谱柱(4.6mm×250mm,5μm);以乙N-0.5%磷酸二氢钾(38:62)为流动相;检测波长为296nm;流速为1.0mL·min^-1结果:在建立的色谱条件下,华蟾酥毒基的回归方程为Y=1000000 X-648.2,r=0.9990,表明华蟾酥毒基在0.0139~0.695μg与峰面积积分值呈良好线性关系;脂蟾毒配基的回归方程为Y:5000000X+42394,r=0.9995,脂蟾毒配基在0.0210~1.0525μg与峰面积积分值呈良好线性关系。结论:本法简便、快捷,准确度高,专属性强,重现性好,可用于华蟾酥毒基、脂蟾毒配基的含量测定。
Objective: To establish a HPLC method to determine the contents of cinobufagin and resibufogenin for chief components of venenum bufonis in tianfushen oral solution. Methods: The method were determined by HPLC with Waters SymmetryShieldTM RP18 (4. 6 mm× 250 mm,5μm) as column, a mixture of acetonitrile :0. 5 % potassium dihdyrogen phosphate (38:62) as mobile phase, UV detector at 296nm and flow rate of 1.0mL.min^-1 Results: The calibration curves are linear in the range of 0. 013 9 -0. 695 μg for cinobufagin(r =0. 999 0), 0. 021 0 - 1. 052 5 μg (r = 0. 999 5) for resibufogenin, respectively, regression equations were Y = 1 000 000 X - 648. 2 and Y = 5 000 000 X + 42 394, respectively. Conclusion: The method is simple, rapid and accurate, which can be used to determine chief components of venenum bufonis in tianfushen oral solution.
出处
《中国现代中药》
CAS
2010年第10期35-37,共3页
Modern Chinese Medicine