首页> 外文期刊>Journal of Analytical Methods in Chemistry >Identification and Differentiation of Polygonum multiflorum Radix and Polygoni multiflori Radix Preaparata through the Quantitative Analysis of Multicomponents by the Single-Marker Method
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Identification and Differentiation of Polygonum multiflorum Radix and Polygoni multiflori Radix Preaparata through the Quantitative Analysis of Multicomponents by the Single-Marker Method

机译:通过单标法定量分析多组分的鉴定与分化多粒子型多粒子和PolyGONI Multiflori基拉帕水准

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The quantitative analysis of multicomponents by the single-marker (QAMS) method was established and the relationship between F value (the ratio of the sum of the contents of emodin-8-O-β-D-glucopyranoside and physcion-8-O-β-D-glucopyranoside to the sum of the contents of emodin and physcion) and the steaming time was found to identify and differentiate Polygonum multiflorum Radix and its processed product. Emodin was considered as the control substance, and the correction factors of physcion, emodin-8-O-β-D-glucopyranoside, and physcion-8-O-β-D-glucopyranoside were computed. In addition, the contents of the four components were determined. When the F value is greater than or equal to 1.0, the sample was identified as Polygonum multiflorum Radix, and if the F value was between 0.6 and 1.0, the sample of Polygoni multiflori Radix Preaparata was processed incompletely. The F value of the qualified Radix Polygonum multiflorum should be no more than 0.6. However, the influence of different sample injection volumes and the chromatographic columns and instruments used on the durability of the correction factors and RSD ≤3% hindered accurate identification; therefore, a QAMS method using an external standard value with methodological verification was developed. We redefined the “Polygonum multiflorum rules.” The method using “Polygonum multiflorum rules” revised after optimization of the determination results was used, as it was accurate and led to convenient operation and low inspection costs, and moreover, the method could differentiate Polygoni multiflori Radix Preaparata and Polygonum multiflorum Radix medicinal samples and precisely identify samples that were different from the completely processed product Polygoni multiflori Radix Preaparata.
机译:通过单标记(QAMS)方法进行多组分的定量分析,F值与大素-8-o-β-D-葡糖苷和物理-8-O-的关系的关系发现β-D-吡喃吡喃糖苷与大黄素和物理液的含量之和)和蒸汽时间识别和分化多糖型百分子混浊及其加工产品。将大黄素被认为是对照物质,并且计算了物理化,外素-80-β-D-吡喃葡萄糖和物理-8-O-β-D-葡糖葡萄糖苷的校正因子。此外,确定了四种组分的内容物。当F值大于或等于1.0时,将样品鉴定为volygonum multifllum radix,如果f值在0.6和1.0之间,则Polygoni Multiflori基数预先处理的样品不完全处理。合格的基数型多粒子的F值不应超过0.6。然而,不同样品注入体积和色谱柱和仪器用于耐用性的耐用性和RSD≤3%的影响,阻碍了精确识别;因此,开发了使用具有方法验证的外标值的QAMS方法。我们重新定义了“Polygonum Multiflorum规则”。使用“多谷型Multiflorum规则”在优化测定结果的优化后进行了修订的方法,因为它准确并导致了方便的操作和低检查成本,此外,该方法可以区分Polygoni Multiflori基数预脂肪酸数据和多脂肪族百分子基质的药物样品精确地识别与完全加工的产品PolyGoni Multiflori Radix预征的样本。

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