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作 者:赵亮[1] 吴豪[2] 张海[1] 吕磊[1] 朱臻宇[2] 张国庆[1] 柴逸峰[2]
机构地区:[1]第二军医大学附属东方肝胆外科医院药材科,上海200438 [2]笫二军医大学药学院,上海200433
出 处:《药学实践杂志》2013年第6期432-435,共4页Journal of Pharmaceutical Practice
摘 要:目的优化牡丹皮提取条件,建立同时测定牡丹皮中没食子酸、芍药苷和丹皮酚3种有效成分含量的反相高效液相色谱分析方法。方法采用Agilent Plus C18柱,以乙腈-0.6%甲酸水溶液为流动相,梯度洗脱,流速1.0ml/min,检测波长254nm,进样量10μl。结果回归方程分别为:没食子酸Y=16.5980X+4.9502,r=0.9999;芍药苷Y=1.6131X+0.9951,r=0.9999;丹皮酚Y=5.9817X+54.1030,r=0.9997。线性范围分别为4.0~100.1;20.6~515.0;33.3~832.0μg/ml。平均回收率分别为100.7%、99.2%、97.8%;RSD(n=9)分别为1.6%、3.0%、1.1%。结论考察了牡丹皮的提取条件,提取效果良好,分析方法准确可靠,重复性好,回收率高,适用于牡丹皮的含量测定。Objective To optimize the extraction methods and develop a HPLC-DAD assay for the determination of three effective ingredients in Moutan Coretex. Methods The analysis was performed on an Agilent ZORBAX Eclipse Plus (4.6 mm ×150 mm, 5 μm) column with acetonitrile and water (0.6% formic acid) as mobile phase at a rate of 1.0 ml/min, the detection wavelength was 254 nm, the injection volume was 10 p.1. Results The regress equation of gallic acid, paeoniflorin and paeonol were Y = 16. 598 0X + 4. 950 2, r = 0. 999 9 ; Y = 1. 613 1X + 0. 995 1, r = 0. 999 9 ; Y = 5.981 7X + 54. 103 0, r = 0. 999 7, respectively. The average recoveries were 100.7% , 99.2% , 97.8% and RSD(n =9) were 1.6% , 3.0% , 1.1%. Conclusion The extraction effect was good and the determination assay was reliable and accurate.
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