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首页> 外文期刊>Journal of liquid chromatography and related technologies >Analysis of five pharmacologically active compounds from the Tibetan medicine Elsholtzia with micellar electrokinetic capillary chromatography
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Analysis of five pharmacologically active compounds from the Tibetan medicine Elsholtzia with micellar electrokinetic capillary chromatography

机译:胶束电动毛细管色谱法分析藏药Elsholtzia中的5种药理活性化合物

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摘要

A high performance capillary electrophoresis method with diode array detector detection for the determination of five bioactive ingredients in Tibetan medicine Elsholtzia, namely quercetin, rutin, saussurenoside, kaempferol, and oleanolic acid, has been developed. The effects of several factors, such as the acidity, concentration of running buffer, separation voltage, temperature, and SDS concentration were investigated. The optimal conditions were 44 mmol/L boric acid running buffer (pH 8.5), 45 mmol/L SDS, 16 KV voltage, 20 degrees C, and 10.0% (V/V) of acetonitrile. Under the optimum conditions, five components could be separated with a good baseline resolution within 17 min. The calibration curves showed good linear relationship over the concentration range of 5 x 10(-4)similar to 0.1 mg/mL for quercetin, rutin, saussurenoside, kaempferol, and 1 x 10(-3) similar to 0.1 mg/mL for oleanolic acid. The average recoveries of the method and RSD were ( 99.2%, 3.2%) for quercetin, (102.1%, 2.1%) for rutin, (99.4%, 1.5%) for saussurenoside, (98.9%, 1.8%) for kaempferol, and (99.0%, 2.9%) for oleanolic acid, respectively. The detection limits (S/N = 3) were 1.1 x 10(-4) mg/mL for quercetin, 2.6 x 10(-4) mg/mL for rutin, 1.8 x 10(-4) mg/mL for saussurenoside, 2.9 x 10(-4) mg/mL for kaempferol, and 6.3 x 10(-4) mg/mL for oleanolic acid, respectively. The method was simple, rapid, and reproducible and could be applied for the determination of quercetin, rutin, saussurenoside, kaempferol, and oleanolic acid in Tibetan medicine Elsholtzia, and the assay results were satisfactory.
机译:已开发出一种具有二极管阵列检测器检测功能的高效毛细管电泳方法,用于测定藏药Elsholtzia中的5种生物活性成分,即槲皮素,芦丁,雪莲糖苷,山奈酚和齐墩果酸。研究了酸度,运行缓冲液浓度,分离电压,温度和SDS浓度等几个因素的影响。最佳条件为44 mmol / L硼酸运行缓冲液(pH 8.5),45 mmol / L SDS,16 KV电压,20摄氏度和10.0%(V / V)的乙腈。在最佳条件下,可以在17分钟内以良好的基线分辨率分离出五个成分。校准曲线在5 x 10(-4)的浓度范围内显示出良好的线性关系,其中槲皮素,芦丁,鼠李糖苷,山奈酚的浓度范围接近于0.1 mg / mL,而1 x 10(-3)的齐墩果酸含量类似于0.1 mg / mL酸。槲皮素的该方法和RSD的平均回收率分别为(99.2%,3.2%),芦丁(102.1%,2.1%),沙丁胺糖苷(99.4%,1.5%),山奈酚(98.9%,1.8%)和齐墩果酸分别为(99.0%,2.9%)。槲皮素的检出限(S / N = 3)为1.1 x 10(-4)mg / mL,芦丁的检出限为2.6 x 10(-4)mg / mL,雪莲糖苷的检出限为1.8 x 10(-4)mg / mL,山emp酚的含量为2.9 x 10(-4)mg / mL,齐墩果酸的含量为6.3 x 10(-4)mg / mL。该方法简便,快速,重现性好,可用于藏药香s中槲皮素,芦丁,雪莲糖苷,山奈酚和齐墩果酸的测定,测定结果令人满意。

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