Suppr超能文献

制剂中的山奈酚和芹菜素:质量控制的附加标志物?

Rhodiosin and herbacetin in preparations: additional markers for quality control?

机构信息

a Faculty of Pharmacy, Department of Pharmacognosy, University of Szeged , Szeged , Hungary.

b Interdisciplinary Centre for Natural Products, University of Szeged , Szeged , Hungary.

出版信息

Pharm Biol. 2019 Dec;57(1):295-305. doi: 10.1080/13880209.2019.1577460.

Abstract

L. (Crassulaceae) is well-known to contain flavonoids such as the herbacetin derivative rhodiosin. However, flavonoids are not typically used in quality control. This study analyses two flavonoids of rhizomes and roots for their potential as analytical markers. Two constituents were isolated from ethanolic extracts via HPLC, identified via NMR and quantified via RP-HPLC. Presence and content variation was investigated according to extraction (solvent and repetitions), drying (temperature and duration) and sample origin (homogenously cultivated plants of different provenance, commercial samples). Rhodiosin was identified as a main flavonoid, accompanied by 10-fold lower concentrated herbacetin. Both compounds were best extracted with 70-90% ethanol, but were also detectable in more aqueous extracts. Different drying conditions had no effect on the flavonoid content. These two flavonoids were consistently identified in rhizome and root extracts of over 100 samples. Rhizomes tend to contain less flavonoids, with average ratios of rosavins to flavonoids of 1.4 (rhizomes) and 0.4 (roots). Provenance differences were detected in the range (rhodiosin plus herbacetin) of 760-6300 µg/mL extract corresponding to a maximum of approximately 0.5-4.2% (w/w) in the dry drug. For the first time, two main flavonoids present in were quantified systematically. Rhodiosin and herbacetin can be detected simultaneously to phenylpropenoids or salidroside in authentic samples, influenced by the plant part examined and the plant origin. Rhodiosin and herbacetin may serve as additional marker to guarantee a consistent content of products.

摘要

(景天科)以含有类黄酮如草芍药苷衍生的草红定而闻名。然而,类黄酮通常不用于质量控制。本研究分析了根茎和根中的两种类黄酮,以评估它们作为分析标记物的潜力。两种成分通过 HPLC 从乙醇提取物中分离出来,通过 NMR 鉴定,并通过 RP-HPLC 定量。根据提取(溶剂和重复次数)、干燥(温度和时间)和样品来源(不同来源的均匀种植植物、商业样品)来研究其存在和含量变化。草红定被鉴定为主要类黄酮,同时伴有浓度低 10 倍的草芍药苷。这两种化合物都能用 70-90%乙醇最佳提取,但也能在更水性的提取物中检测到。不同的干燥条件对类黄酮含量没有影响。这两种类黄酮在 100 多个样品的根茎和根提取物中都能一致地被识别。根茎中类黄酮的含量较低,罗莎文与类黄酮的平均比值为 1.4(根茎)和 0.4(根)。在提取物中(草红定加草芍药苷)的范围内检测到了产地差异,范围为 760-6300µg/mL,相当于干药材中 0.5-4.2%(w/w)的最大值。首次系统地对 中存在的两种主要类黄酮进行了定量。草红定和草芍药苷可以与苯丙素或红景天苷同时检测到,受所检查的植物部分和植物来源的影响。草红定和草芍药苷可作为额外的标记物,以保证 的含量一致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b1d/6711108/b3cc36a6548e/IPHB_A_1577460_F0001_B.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验