首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >High-performance liquid chromatography analysis of polyacetylenes and polyenes in Echinacea pallida by using a monolithic reversed-phase silica column
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High-performance liquid chromatography analysis of polyacetylenes and polyenes in Echinacea pallida by using a monolithic reversed-phase silica column

机译:整体式反相硅胶柱高效液相色谱分析紫锥菊中的聚乙炔和多烯

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In this study, a RP-HPLC method for the analysis of polyacetylenes and polyenes in Echinacea pallida roots and phytopharmaceuticals was developed. The reference compounds used for quantification were isolated from the plant material and their structures were determined on the basis of the analysis of UV, IR, NMR and MS data. The complete structure elucidation of three compounds, namely 8-hydroxy-tetradec-(9E)-ene-11, 13-diyn-2-one (1), tetradec-(8Z)-ene-11,13-diyn-2-one (6) and pentadec-(8Z)-en-2-one (9) is described. In the analysis of the n-hexane extracts of E. pallida roots, the comparison between conventional and monolithic columns showed that the elution order in both cases is identical and the selectivity is equivalent. However, the retention times achieved by the monolithic column are shorter, resulting in a faster separation (20 min). Therefore, the analyses were carried out on a Chromolith Performance RP-18c (100 mm x 4.6 mm i.d.), with a gradient mobile phase composed by H2O and ACN at the flow rate of 2 mL/min. The column was thermostatted at 20 degrees C. The photodiode array detector monitored the eluent at 210nm. The validation procedure confirmed that this technique affords reliable analysis of these components and is appropriate for the quality control of complex matrices, such as E. pallida roots and phytopharmaceuticals. (c) 2006 Elsevier B.V. All rights reserved.
机译:在这项研究中,建立了一种RP-HPLC分析紫锥菊和植物药中的聚乙炔和多烯的方法。从植物材料中分离出用于定量的参考化合物,并根据对UV,IR,NMR和MS数据的分析确定其结构。阐明三种化合物的完整结构,即8-羟基-十四烷基-(9E)-ene-11、13-二炔-2-酮(1),十四烷基-(8Z)-烯-11,13-diyn-2-描述了一个(6)和十五(8Z)-en-2-一个(9)。在对大肠埃希氏菌根的正己烷提取物进行分析时,常规色谱柱和整体色谱柱之间的比较表明,两种情况下的洗脱顺序均相同,且选择性相同。但是,通过整体柱实现的保留时间更短,从而实现了更快的分离(20分钟)。因此,分析是在Chromolith Performance RP-18c(内径100 mm x 4.6 mm)上进行的,流动相由H2O和ACN组成,流速为2 mL / min。将该柱恒温在20℃。光电二极管阵列检测器监测210nm的洗脱液。验证程序证实,该技术可对这些成分进行可靠的分析,适用于复杂基质的质量控制,例如淡色肠球菌根和植物药物。 (c)2006 Elsevier B.V.保留所有权利。

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