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作 者:王光发[1] 廖正根[1] 梁新丽[1] 赵国巍[1]
机构地区:[1]江西中医学院现代中药制剂教育部重点实验室,南昌市330004
出 处:《中国药房》2009年第9期672-674,共3页China Pharmacy
基 金:国家科技支撑计划子课题(2006BAI09B07-05);江西省自然科学基金资助项目(2007GZY0932)
摘 要:目的:建立以高效液相色谱法同时测定元胡止痛片中延胡索乙素、欧前胡素和异欧前胡素含量的方法。方法:色谱柱为Zorbax Extend-C18(250mm×4.6mm,5μm),流动相为乙腈-0.1%磷酸溶液(三乙胺调pH6.5,梯度洗脱),流速为1mL·min-1,柱温为25℃。结果:延胡索乙素、欧前胡素、异欧前胡素的检测浓度分别在10.2~51.0、2.5~12.5、2.2~11.0μg·mL-1(均r=0.9999)范围内与各自峰面积积分值呈良好的线性关系;三者加样回收率分别为97.89%、101.77%、99.04%,RSD分别为0.8%、1.4%、1.3%(均n=9)。结论:本方法简便、快速、准确,可用于元胡止痛片的质量控制。OBJECTIVE: To develop an HPLC method for simultaneous determination of tetrahydropalmatine, imperatorin and isoimperatorin in Yuanhu zhitong tablet. METHODS: The sample was separated on A Zorbax Extend - C18 column (250 mm ×4.6 mm, 5 μm) at column temperature of 25℃ . The mobile phase consisted of acetonitrile - 0.1% phosphoric acid solution (adjusted pH to 6.5 by triethylamine, gradient elution) at a flow rate of 1 mL·min^-1. RESULTS: The linear ranges of tetrahydropalmatine, imperatorin and isoimperatorin were 10.2--51.0μg ·mL^-1( r - 0.999 9), 2.5- 12.5μg·mL^-1( r = 0.999 9) and 2.2-11.0μg·mL^-1( r = 0.999 9) respectively, and their average recovery rates were 97.89% (RSD = 0.8%, n = 9), 101.77% (RSD = 1.4%, n = 9) and 99.04% (RSD - 1.3%, n = 9), respectively. CONCLUSION: The method is simple, rapid, accurate, and applicable for the quality control of Yuanhu zhitong tablet.
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