普通蓍草(Achillea Millefolium L.)的定性和定量分析现状

A. Vaskova, V. Kurkin
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引用次数: 0

摘要

目的建立一种对千叶水蛭中黄酮类化合物进行定性和定量分析的方法。该研究的材料是2020年和2021年收获的蓍草,以及来自“Krasnogorskleksredstva”JSC的工业样本。此外,我们使用了黄酮类化合物的参考样品:芦丁、槲皮素、山奈酚、cynaroside和木犀草素,这些样品是我们之前在研究含有黄酮类化合物的原料时收到的,并使用NMR、UV和质谱进行了描述。采用薄层色谱法(定性分析)鉴定真伪。采用差示分光光度法对总黄酮进行定量分析,方法参照药典专著1.2.1.1.0003.15《紫外和可见光谱分光光度法》。用分光光度计“Specord 40”(Analytik Jena AG,德国)在层厚为10 mm的比色皿中标记水乙醇提取物的光谱特征。结果。根据真伪鉴定结果,在365 nm紫外光(试剂AlCl3)下发现了3个具有亮黄色辉光的吸附区,其中1个吸附区位于柴黄苷标准品溶液色谱中的吸附区,其Rf值为0.7。在参比样品中,cynaroside的优势吸附区为r1.3,推测其为cosmosiin,而在山奈酚标准样品中,其吸附区为r0.8。所得数据证实了西纳罗苷在普通蓍草中草药中的存在,也为以西纳罗苷为参比样品对给定原料进行定性和定量分析提供了可能。以杨梅苷为参比样品,采用差示分光光度法,波长为400 nm,建立了杨梅中总黄酮含量的定量测定方法。黄酮含量为0.410.02% ~ 0.740.03%(相当于杨梅苷)。单次测定的误差为6.70%,95%置信区间。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Current aspects of qualitative and quantitative analysis of common yarrow (Achillea Millefolium L.)
Aim to develop a methodology for qualitative and quantitative analysis of flavonoids in the herb of Achillea millefolium L. Material and methods. The material of the study was the yarrow herb harvested in 2020 and 2021, and an industrial sample from JSC "Krasnogorskleksredstva". Additionally, we used the reference samples of flavonoids: rutin, quercetin, kaempferol, cynaroside, and luteolin, received previously during our studies of the raw materials containing the flavonoids and described using the NMR, UV and mass spectroscopy. The authenticity was determined by the thin layer chromatography (qualitative analysis). For the quantitative analysis of the total flavonoids, we used the differential spectrophotometry, conducted in accordance with Pharmacopoeial monograph 1.2.1.1.0003.15 "Spectrophotometry in ultraviolet and visible spectra". The spectral characteristics of the water-ethanolic extractions were marked using the spectrophotometer "Specord 40" (Analytik Jena AG, Germany), in cuvettes with layer thickness of 10 mm. Results. Based on the results of the authenticity determination, we revealed three adsorption zones with bright yellow glow in UV light at a wavelength of 365 nm (reagent AlCl3), one of which was at the level of the adsorption zone in the chromatogram of the solution of standard sample of cinaroside with a value of Rf 0.7. The dominant adsorption zone with a value of Rs 1.3 in respect to the reference sample of cynaroside was presumably attributed to cosmosiin, while the adsorption zone with a value of Rf 0.8 was detected at the level of standard sample of kaempferol. The obtained data confirmed the presence of cynaroside in the herb of common yarrow, and also the possibility to conduct the qualitative and quantitative analysis of the given raw material with the use of cynaroside as a reference sample. We developed the method of quantitative determination of the total flavonoids in yarrow herb using a reference sample of cynaroside and differential spectrophotometry at an analytical wave length of 400 nm. The content of the total flavonoids for the common yarrow herb varied from 0.410.02% to 0.740.03% (equivalent to cynaroside). The error of single determination with 95% confidence interval was 6.70%.
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