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作 者:李坤平[1,2] 潘天玲[2] 周宏兵[2] 李卫民[1]
机构地区:[1]广州中医药大学中药学院,广州510006 [2]广东药学院药科学院,广州510006
出 处:《理化检验(化学分册)》2010年第9期1060-1062,共3页Physical Testing and Chemical Analysis(Part B:Chemical Analysis)
基 金:广东省科技计划项目(2006B35605005)
摘 要:提出了反相高效液相色谱法同时测定布渣叶的3种水解黄酮苷元槲皮素、山奈酚和异鼠李素的含量。采用Kromasil C18色谱柱(250 mm×4.6 mm,5μm),以甲醇-0.4%(体积分数)磷酸溶液为流动相梯度洗脱,在368 nm波长处,对布渣叶的水解液进行了色谱分离测定。结果表明:槲皮素的质量浓度在1.97-19.7 mg·L^-1,山奈酚在2.02-20.2 mg·L^-1,异鼠李素在2.11-21.1 mg·L^-1时分别与其峰面积呈线性关系。槲皮素、山奈酚和异鼠李素的加标回收率分别为93.0%-99.6%,92.6%-99.8%,92.5%-99.5%,相对标准偏差(n=6)分别为2.48%,2.80%,3.17%。RP-HPLC was applied to the simultaneous determination of 3 flavonoid aglycone hydrolyzates including quercetin,kaempferol and isorhamnetin by hydrolysis of leaves of Microcos paniculata L.from different regions.The hydrolyzed solution of sample was separated by gradient elution with methanol and 0.4%(φ) phosphoric acid solution on Kromasil C18 column(250 mm×4.6 mm,5 μm),and their contents determined at the wavelength 368 nm.Linear relationships between values of peak area and mass concentration of quercetin,kaempferol and isorhamnetin were kept in ranges of 1.97-19.7 mg·L^-1,2.02-20.2 mg·L^-1,and 2.02-20.2 mg·L^-1,respectively.Tests for recovery and precision were made by standard addition method,giving values of recovery in the range of 93.0%-99.6%,(quercetin),92.6%-99.8%(kaempferol) and 92.5%-99.5%(isorhamnetin).Values of RSD′s(n=6) found were 2.48% for quercetin,2.80% for kaempferol and 3.17% for isorhamnetin.
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