Suntornsuk Leena, Kasemsook Saowapak, Wongyai Surapote
Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Mahidol University, Rajathevee, Bangkok, Thailand.
Electrophoresis. 2003 Apr;24(7-8):1236-41. doi: 10.1002/elps.200390159.
A capillary zone electrophoresis method was established for analysis of aglycone quercetin in mulberry leaves (Morus alba L.). The influence of, e.g., background electrolyte concentrations and pH, surfactant concentrations, organic solvents, temperature, and voltage on the separation of aglycone quercetin, rutin, quercitrin, kaempferol, catechin, and gallic acid was systematically investigated. The optimum condition providing baseline separation of all compounds within 16.5 min was obtained in 150 mM boric acid (pH 10.0) using a fused-silica capillary with an effective length of 42.5 cm (50 microm inner diameter), temperature of 32 degrees C, and voltage of 15 kV. Method assessment was performed by standard addition method using rutin as an internal standard. Linearity of the method was excellent (r(2) > 0.999) over the concentration tested (40-160 microg/mL). The relative standard deviations (%RSDs) from injection, intraday, and interday precision were less than 2.5%. Recoveries were good (asymptotically equal to 100.0%,%RSD = 0.8%) with a limit of detection (LOD) and limit of quantitation (LOQ) of 0.86 and 3.16 microg/mL (%RSD = 1.8%), respectively. The aglycone quercetin found in the mulberry leaves was 0.452 g/100 g (%RSD = 0.6%) on dry weight.
建立了一种毛细管区带电泳法用于分析桑叶(桑科植物桑)中的槲皮素苷元。系统研究了背景电解质浓度和pH值、表面活性剂浓度、有机溶剂、温度和电压等因素对槲皮素苷元、芦丁、槲皮苷、山奈酚、儿茶素和没食子酸分离的影响。在150 mM硼酸(pH 10.0)中,使用有效长度为42.5 cm(内径50μm)的熔融石英毛细管,温度为32℃,电压为15 kV,在16.5分钟内实现了所有化合物的基线分离,获得了最佳条件。采用以芦丁为内标的标准加入法进行方法评估。在所测试的浓度范围(40 - 160μg/mL)内,该方法的线性良好(r²>0.999)。进样、日内和日间精密度的相对标准偏差(%RSD)均小于2.5%。回收率良好(近似等于100.0%,%RSD = 0.8%),检测限(LOD)和定量限(LOQ)分别为0.86和3.16μg/mL(%RSD = 1.8%)。桑叶中发现的槲皮素苷元干重为0.452 g/100 g(%RSD = 0.