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作 者:陈燕[1] 黄志芳[1] 德吉 刘云华[1] 易进海[1]
机构地区:[1]四川省中医药科学院,四川成都610041 [2]西藏自治区藏医院,西藏拉萨850000
出 处:《中国执业药师》2009年第2期36-38,共3页China Licensed Pharmacist
摘 要:目的:建立全缘绿绒蒿药材中槲皮素的薄层色谱鉴别与含量测定方法。方法:采用TLC法对全缘绿绒蒿进行鉴别;采用HPLC法测定槲皮素含量,色谱条件为:色谱柱,Phenomenex LunaC18(2)(4.6mm×150mm,5μm);流动相,甲醇-0.4%磷酸溶液(50∶50);检测波长,360nm;流速,0.8ml/min。柱温:35℃。结果:各批全缘绿绒蒿药材TLC色谱中均能检出槲皮素;槲皮素HPLC色谱峰与其它色谱峰分离良好,进样量在0.04304~0.25824μg范围内,呈良好线性关系(r=0.9998),平均回收率为97.14%,RSD=1.24%(n=6)。结论:本法简便快捷,结果可靠,为控制全缘绿绒蒿药材的质量提供参考。Objective: To establish the TLC identification and quantitative determination methods of Meconopsis integrifplia. Method: TLC and HPLC were adopted to identify and determine Meconopsis integrifplia. The chromatographic conditions were Pbenomenex Luna C18(2), (4.6 mm× 150 mm, 5μm)column as analytic column, methanol-0.4%H3PO4 water solution (50 i 50) as mobile phase, detection wavelength at 360nm; column temperature at 35 ℃, flow rate at 0.8ml/min. Results: Quercetin was identified by TLC and determined by ttPLC. The liner range of quercetin was 0.043 0400.258 24μg, r - 0.999 8, The average recovery was 97.14%, RSD-1.24%(n=6). Conclusion: These methods are simple, accurate, reproducible and can be used to enhance the quality control of this drug.
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