首页> 外文期刊>Analytical chemistry >Determination of Saikosaponin Derivatives in Radix bupleuri and in Pharmaceuticals of the Chinese Multiherb Remedy Xiaochaihu-tang Using Liquid Chromatographic Tandem Mass Spectrometry
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Determination of Saikosaponin Derivatives in Radix bupleuri and in Pharmaceuticals of the Chinese Multiherb Remedy Xiaochaihu-tang Using Liquid Chromatographic Tandem Mass Spectrometry

机译:液相色谱-串联质谱法测定柴胡及中药小柴胡汤中的皂苷皂苷衍生物

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Saikosaponins are bioactive oleanane saponins derived from the Chinese medicinal herb Radix bupleuri ("chaihu" in Chinese). An LC-MS/MS-based method has been developed for characterization and quantification of 15 saikosaponin derivatives (saikosaponin a, saikosaponin b_(1), saikosaponing, saikogenin A, saikogenin H, saikosaponin c, saikosaponin h, saikosaponin i, prosaikogenin C_(2), prosaikogenin B_(2), saikogenin C, saikogenin B, saikosaponin d, saikosaponin b_(2), and saikogenin D) in one chromatographic run. Optimization of the ionization process was performed with electrospray and atmospheric pressure chemical ionization techniques in both positive and negative ion modes. Negative ion ESI was adopted for generation of the precursor deprotonated molecules to achieve the best ionization sensitivity for the analytes. In addition, the most abundant fragment ion was chosen for each analyte to give the best CID sensitivity. Because some of the saponin derivatives are isomeric, complete resolution for the whole analytes was achieved both chromatographically and mass spectroscopically. Furthermore, optimal internal standard was successfully discovered for determination of the analytes by making use of a combinatorial chemistry approach. Good linearity over the range ~1.65 or 4.98 to 1200 ng/mL for the analytes was observed. The intraday accuracy and precision at nominal low, intermediate, and high concentration varied between 0.8 and 11.8% and between 80 and 116%, respectively, whereas those for interday assay were between 1.1 and 15.5% and between 86 and 119%, respectively. The lower limits of quantitation for the test compounds were ~16.5 to 49.4 pg on-column. The new method offered higher sensitivity and greater specificity than previously reported LC methods. After the validation, the applicability of the method for determination of these chemicals present in a variety of crude chaihu roots and in different brands of the Chinese multiherb remedy Xiaochaihu-tang (or Shosaiko-to) extract granules has been demonstrated. The sensitivity and specificity of the technique will be the basis of a method for the accurate quantification of the saikosaponin derivatives in biomatrixes.
机译:柴胡皂苷是具有生物活性的齐墩果皂苷,其衍生自中草药柴胡(柴胡)。已开发出一种基于LC-MS / MS的方法来表征和定量15种皂苷皂苷衍生物(皂苷皂苷a,皂苷皂苷b_(1),皂苷皂苷,皂苷皂苷A,皂苷皂苷H,皂苷皂苷c,皂苷皂苷h,皂苷皂苷i,皂苷皂苷C_( 2),prosaikogenin B_(2),saikogenin C,saikogenin B,saikosaponin d,saikosaponin b_(2)和saikogenin D)在一次色谱运行中。电离过程的优化是通过电喷雾和大气压化学电离技术在正离子和负离子模式下进行的。采用负离子ESI生成前质子去质子化分子,以实现对分析物的最佳电离灵敏度。此外,为每种分析物选择了最丰富的碎片离子,以提供最佳的CID灵敏度。由于某些皂苷衍生物是异构体,因此在色谱和质谱上均可实现整个分析物的完全分离。此外,通过组合化学方法,成功地找到了用于测定分析物的最佳内标。在分析物的〜1.65或4.98至1200 ng / mL范围内观察到良好的线性。在标称低,中和高浓度下,日间准确性和精密度分别在0.8和11.8%之间以及80和116%之间变化,而日间分析的日间准确性和精确度分别在1.1和15.5%之间以及在86和119%之间。待测化合物的定量下限为〜16.5 pg至49.4 pg柱上。与以前报道的液相色谱方法相比,新方法具有更高的灵敏度和特异性。验证之后,已证明该方法可用于测定各种粗柴胡根中以及不同牌子的中药材小柴胡汤提取物中的这些化学物质。该技术的灵敏度和特异性将成为准确定量生物基质中皂苷皂苷衍生物的方法的基础。

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