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首页> 外文期刊>Chinese Medicine >A multivariate analysis on the comparison of raw notoginseng (Sanqi) and its granule products by thin-layer chromatography and ultra-performance liquid chromatography
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A multivariate analysis on the comparison of raw notoginseng (Sanqi) and its granule products by thin-layer chromatography and ultra-performance liquid chromatography

机译:薄层色谱法和超高效液相色谱法对三七原料及其颗粒产品进行比较的多元分析

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Background Granule products produced from medicinal herbs are gaining popularity. However, there have been few studies comparing the quality or efficacy of granules with those of herbal formulations. This study aims to compare commercially available notoginseng (Sanqi in Chinese) in both raw and granule forms by thin layer chromatography (TLC) and ultra-performance liquid chromatography with photodiode array detection (UPLC-PDA) using multivariate analysis. Methods Aqueous extracts of the raw herb (collected from six different sources in China) and granule products (purchased in China, Taiwan and Australia) were re-extracted with methanol to remove water-soluble excipients. Five compounds (ginsenosides Rg1, Rg2, Rd and Rb1 and notoginsenoside NR1) in the methanolic extracts were quantified by TLC and UPLC-PDA. Multivariate statistical analysis using hierarchical component analysis (HCA) and principal component analysis (PCA) was used to determine the similarities between the granule products and raw herbs. A 2,2′-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) assay was used to measure the antioxidant capacities of the extracts. Results HCA and PCA of the TLC analysis clustered the granule products into one group. By UPLC analysis, the raw herbs and two of the granule products (G7 and G12) were allocated into Group 1 and the rest of the granule products into Group 2. The contents of the five marker compounds in Group 1 were higher than Group 2 and also exhibited stronger ABTS activity (P?=?0.005). By Pearson correlation, the contents of the five compounds in the samples were positively and significantly correlated to their antioxidant activities. Conclusions UPLC was more efficient than TLC for the simultaneous determination of the five major compounds in Sanqi products in terms of linearity, higher sensitivity and repeatability. The statistical analysis of the samples by HCA and PCA revealed that the contents of the marker compounds were significantly higher in the raw herb group than the granule group.
机译:背景技术由草药制成的颗粒产品越来越受欢迎。然而,很少有研究比较颗粒剂和草药制剂的质量或功效。这项研究旨在通过薄层色谱(TLC)和超高效液相色谱与光电二极管阵列检测(UPLC-PDA)进行多变量分析,比较市售的三七(生三七)和颗粒形式。方法用甲醇对粗制草药的水提物(从中国的六种不同来源收集)和颗粒产品(在中国,台湾和澳大利亚购买)进行再萃取,以去除水溶性赋形剂。通过TLC和UPLC-PDA对甲醇提取物中的五种化合物(人参皂苷Rg1,Rg2,Rd和Rb1和三七皂苷NR1)进行了定量。使用分层成分分析(HCA)和主成分分析(PCA)进行多变量统计分析,以确定颗粒产品和生药材之间的相似性。 2,2'-叠氮基双(3-乙基苯并噻唑啉-6-磺酸)(ABTS)测定法用于测量提取物的抗氧化能力。结果TLC分析的HCA和PCA将颗粒产品分为一组。通过UPLC分析,将生药和两种颗粒产品(G7和G12)分配到第1组,其余颗粒产品分配到第2组。第1组中5种标记物的含量高于第2组和第2组。还表现出更强的ABTS活性(P≥0.005)。通过皮尔森相关性,样品中五种化合物的含量与其抗氧化活性呈正相关且显着相关。结论在线性,更高的灵敏度和可重复性方面,UPLC比三层色谱法同时测定三七产品中的五种主要化合物更有效。通过HCA和PCA对样品进行的统计分析表明,生草药组中标记化合物的含量明显高于颗粒组。

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