CZE Determination of flavornoids in Halenia elliptica
文献类型:期刊论文
作者 | Shi YP(师彦平)![]() ![]() |
刊名 | Chromatographia
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出版日期 | 2006 |
卷号 | 63期号:9/10页码:449-452 |
关键词 | Capillary electrophoresis Pharmaceutical analysis Flavonoid Halenia elliptica Gentianaceae |
ISSN号 | 0009-5893 |
通讯作者 | 师彦平 |
中文摘要 | A capillary zone electrophoretic method with UV detection at 254 nm has been developed and validated for quantitative analysis of three flavonoids, luteolin)7)O)b)D-glycoside, genkwanin, and luteolin, in Halenia elliptica. The applied voltage was 15 kV and the capillary temperature was kept constant at 25 C. The effects on migration of buffer pH, electrolyte concentration, and organic modifier were studied systematically. Optimum separation was achieved with 20 mM borate buffer at pH 9.00 containing10% (v/v) acetonitrile. Regression equations revealed a good linear relationship between the peak area of each compound and its concentration. All correlation coefficients were 0.9999. The relative standard deviations of migration time and peak areas were, respectively, <1.58 and 5.02%(intra-day) and <1.69% and 5.36% (inter-day). The amounts of the three compounds in the different parts of H. elliptica (stems, leaves, and flowers) and in the extracts of the flowers obtained with different solvents (100% methanol and 50% and 75% methanol in water) were successfully determined with satisfactory repeatability and recovery. |
学科主题 | 分析化学与药物化学 |
收录类别 | SCI |
资助信息 | the National Natural Science Foundation of China (NSFC No. 20475057) |
语种 | 英语 |
公开日期 | 2012-10-14 |
源URL | [http://210.77.64.217/handle/362003/1451] ![]() |
专题 | 兰州化学物理研究所_中科院西北特色植物资源化学重点实验室/甘肃省天然药物重点实验室 |
通讯作者 | Shi YP(师彦平); Shi YP(师彦平) |
推荐引用方式 GB/T 7714 | Shi YP,Shi YP. CZE Determination of flavornoids in Halenia elliptica[J]. Chromatographia,2006,63(9/10):449-452. |
APA | 师彦平,&师彦平.(2006).CZE Determination of flavornoids in Halenia elliptica.Chromatographia,63(9/10),449-452. |
MLA | 师彦平,et al."CZE Determination of flavornoids in Halenia elliptica".Chromatographia 63.9/10(2006):449-452. |
入库方式: OAI收割
来源:兰州化学物理研究所
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