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β-环糊精修饰区带毛细管电泳法测定野菊花中的刺槐素、木犀草素和槲皮素

Determination of Acacetin, Luteolin and Quercetin in Chrysanthem indicum L by β-CD modified Capillary Electrophoresis
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摘要 A method was developed to determine acacetin, luteolin and quercetin in Chrysanthem indicum L by β-CD modifiedcapillary electrophoresis. Through the investigation of the effects of buffer pH and concentration, applied voltage, SDS concentration andβ-CD, the analytical conditions were optimized. Under the optimized conditions, the two analytes were well separated in 8 min. A goodlinear relationship between the peak area and concentration was found in the 2-400μg/mL,2-500 μg/mL and 2-500μg/mLconcentration range for acacetin, luteolin and quercetin, respectively. The relative standard deviation based on migration time and peakarea were 0.51%, 0.76%, 0.83% and 2.17%, 2.42%, 2.68% for acacetin, luteolin and quercetin, respectively. The detection limits basedon three time noise were 0.6μg/mL, 0.5μg/mL and 0.6μg/mL for acacetin, luteolin and quercetin, respectively. The method wasverified by real sample analysis and running standard addition and recovery experiments with satisfactory results. A method was developed to determine acacetin, luteolin and quercetin in Chrysanthem indicum L by β-CD modifiedcapillary electrophoresis. Through the investigation of the effects of buffer pH and concentration, applied voltage, SDS concentration andβ-CD, the analytical conditions were optimized. Under the optimized conditions, the two analytes were well separated in 8 min. A goodlinear relationship between the peak area and concentration was found in the 2-400μg/mL,2-500 μg/mL and 2-500μg/mLconcentration range for acacetin, luteolin and quercetin, respectively. The relative standard deviation based on migration time and peakarea were 0.51%, 0.76%, 0.83% and 2.17%, 2.42%, 2.68% for acacetin, luteolin and quercetin, respectively. The detection limits basedon three time noise were 0.6μg/mL, 0.5μg/mL and 0.6μg/mL for acacetin, luteolin and quercetin, respectively. The method wasverified by real sample analysis and running standard addition and recovery experiments with satisfactory results.
出处 《生命科学仪器》 2004年第5期38-39,共2页 Life Science Instruments
基金 “十五”科技攻关重大项目(2001BA210A04-7) 国家自然科学基金(20175025) 国家自然科学基金分析化学重点基金(20235010) 电分析化学国家重点实验室基金 “九五”科技攻关重点项目(96-A23-01-06)的资助
关键词 野菊花 毛细管电泳法 槲皮素 木犀草素 黄酮类化合物 疗效 栓剂 刺槐 花序 有效成分 Capillary Electrophoresis Chrysanthem indicum L Acacetin Luteolin Quercetin
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参考文献4

  • 1北京市野菊花协作组.野菊花制剂临床观察--附454例疗效分析[J].中药通报,1983,8(4):39-40.
  • 2北京第六制药厂.野菊花药理研究及栓剂临床疗效观察[J].中药通报,1985,10(7):45-46.
  • 3[4]Fonseca F. N., Kato M. J., Jr. L. O., et al. Critical assessment of electrolyte system for the capillary electrophoresis analysis of phenolic compounds in herbal extracts. J. Micro. Sep., 2001, 13(6): 227-235
  • 4[5]Li X., Zhang Y., Yuan Z. Determination of baicalin, chlorogenic acid and forsythin in Chinese medicinal preparations by capillary electrophoresis. Chromatographia,2002, 55(7/8): 453-456.

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