摘要
目的: 采用高效液相色谱法测定除痰止嗽丸(CTZSW)中桔梗皂苷D、桔梗皂苷E、白花前胡甲素和白花前胡乙素的含量。 方法: Hypersil C18色谱柱(4.6 mm×150 mm,5 μm),流速1.0 mL·min-1,流动相乙腈-水(35:65)(桔梗皂苷D和桔梗皂苷E),ELSD漂移管温度105 ℃,载气(N2)流速2.6 SLPM·min-1;流动相乙腈-甲醇-水(40:30:30)(白花前胡甲素和白花前胡乙素),检测波长321 nm。 结果: 桔梗皂苷D和桔梗皂苷E分别在0.041 3-0.826 0 μg(r=0.999 7),0.079 7-1.594 0 μg(r=0.999 8)进样量与峰面积呈良好的线性关系,平均加样回收率分别为98.32%,98.94%,RSD(n=6)分别为0.80%,0.93%;白花前胡甲素和白花前胡乙素分别在0.154 9-3.098 0 μg(r=0.999 4),0.051 7-1.034 0 μg(r=0.999 8)进样量与峰面积呈良好的线性关系,平均加样回收率分别为98.72%,99.15%,RSD(n=6)分别为0.86%,0.95%。 结论: 该方法测定结果准确、灵敏、重复性好;可用于除痰止嗽丸的质量评价。
Objective: To develop an HPLC method for determination of the content of platycodin D, platycodin E, praeruptorin A and praeruptorin B in Chutan Zhisouwan. Method: A Hypersil C18 column was used as the chromatographic column. The flow rate was 1.0 mL·min-1. The mobile phase consisted of acetonitrile-water (35:65) for platycodin D and platycodin E, the temperature of drift tube was set at 105 ℃;the gas flow (N2) was set at 2.6 SLPM·min-1.The mobile phase consisted of acetonitrile-methanol-water (40:30:30) for praeruptorin A and praeruptorin B, The UV detection wavelength was set at 321 nm. Result: Platycodin D and platycodin E were linear within the range of 0.041 3-0.826 0 μg (r=0.999 7) and 0.079 7-1.594 0 μg (r=0.999 8) respectively. The average recoveries were 98.32% (RSD 0.80%) and 98.94% (RSD 0.93%). Praeruptorin A and praeruptorin B were linear within the range of 0.154 9-3.098 0 μg (r=0.999 4) and 0.051 7-1.034 0 μg (r=0.999 8) respectively. The average recoveries were 98.72% (RSD 0.86%) and 99.15% (RSD 0.95%). Conclusion: The method was accurate, sensitive and reproducible, which may be used in the determination of platycodin D, platycodin E, praeruptorin A and praeruptorin B in CTZSW.
出处
《中国实验方剂学杂志》
CAS
北大核心
2014年第2期78-82,共5页
Chinese Journal of Experimental Traditional Medical Formulae
基金
北京博士后基金项目(2011M500494)