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作 者:乔怀耀[1] 罗荣[1] 吴娟[1] 朱文漓[1] 柯尊洪[1] 郝晓锋[1] 柯潇[1] 邬智刚
机构地区:[1]成都康弘药业集团股份有限公司,成都610036
出 处:《中国药房》2014年第43期4079-4081,共3页China Pharmacy
基 金:四川省重点技术创新项目(No.2012CD00082);四川省科技成果转化项目(No.2012SC002)
摘 要:目的:建立同时测定舒肝解郁胶囊中金丝桃苷、芦丁含量的方法。方法:采用高效液相色谱法。色谱柱为Agilent Eclipse Plus C18(250 mm×4.6 mm,5μm),流动相为乙腈-甲醇(90∶10,V/V)-50 mmol/L磷酸盐缓冲液(梯度洗脱),流速为0.8 ml/min,检测波长为360 nm,柱温为室温。结果:金丝桃苷和芦丁的进样量分别在1.272~-127.240、1.393-139.350μg范围内与峰面积积分值呈良好线性关系(r=0.9999);二者精密度、稳定性、重复性的RSD〈2%;平均加样回收率分别为96.9%、98.6%(n均为9)。结论:该方法快速、准确,重复性好,可用于舒肝解郁胶囊的质量控制。OBJECTIVE: To develop a method for simultaneous determination of rutin and hyperoside in Shugan jieyu capsule. METHODS:HPLC method was adopted. The determination was performed on Agilent Eclipse Plus C18(250 mm×4.6 mm, 5μm) column with mobile phase consisted of acetonitrile-methanol (90: 10, V/V)-50 mmol/L phosphate buffer (gradient elution) at the flow rate of 0.8 ml/min. The detection wavelength was set at 360 nm, and the column temperature was room temperature. RESULTS: The linear ranges were 1.272-127.240μg for hyperoside and 1.393-139.350μg for rutin, respectively (r=0.999 9). RSDs of precision, stability and reproducibility tests were all lower tharn 2%. The average recoveries were 96.9% and 98.6% (n=9), respectively. CONCLUSIONS : The method is rapid, accurate and repeatable, and can be used for quality control in Shugan jieyu capsule.
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