高效液相色谱-紫外分光光度法鉴别和定量测定几种代表性药材中黄酮类化合物三种植被时间

Q3 Pharmacology, Toxicology and Pharmaceutics Drug Development and Registration Pub Date : 2023-08-30 DOI:10.33380/2305-2066-2023-12-3-134-142
A. M. Poluyanov, A. Yu. Sokolova, A.-D. Koynova, S. D. Kulikova, E. A. Malashenko, N. V. Bobkova
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引用次数: 0

摘要

介绍。研究生物活性物质(以下简称BAS)的积累动态与植物发育的音韵学阶段的关系具有重大的科学和实用意义。黄酮类化合物中苷元和苷类的定量含量取决于植物的生命周期和生长阶段。的目标。目的:鉴定并定量黄酮类化合物。不同植被时期采收的水叶柳、山梨柳和黑叶柳。材料和方法。用该方法从药典文章中提取了所研究植物的地下器官提取物,并进行了分析。采用Nexera-i LC-2040高效液相色谱仪(Shimadzu Corporation, Japan)进行色谱分离和检测。色谱仪配备柱恒温器、色谱柱Grace HPLC-COLUMN 250 × 4.6mm铂C8-EPS 5mm (Grace, США)和保护柱Phenomenex SecurityGuard TM cartridge Widepore C18 4 × 3,0 mm、脱气器、自动进样器(进样量:10µl)和紫外检测器。检测波长为λ = 365±2 nm。流动相含0.1%磷酸水溶液(v/v)(洗脱液A);乙腈(洗脱液B),流速:0.9 ml/min。结果和讨论。对所有研究对象进行分析。采用外标法确认所含物质的真伪,并测定其定量含量。发现并定量的物质为:槲皮素(芦丁)中的3- o -芦丁苷、异鼠李素(水仙素)中的3- o -芦丁苷、山奈酚(黄芪甲苷)中的3- o -葡萄糖苷、木犀草素、山奈酚和异鼠李素。未发现木犀草素7- o -葡糖苷(cynaroside)和7- o - β - d -葡糖苷芹菜素(cosmosiin)。其中木犀草素苷元在总黄酮定量含量中所占比例最大。值得注意的是,在所有研究对象中,与其他类黄酮相比,这种苷元的含量更高,而与植被的阶段无关。结论。在研究过程中,建立了醇水提取物中黄酮类化合物含量的定量测定方法。测定了黄芪地下器官中黄酮类化合物的苷元和苷类成分。3种不同植被下的水杨、山竹和粗叶山竹。
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Identification and Quantitative Determination of Flavonoids by HPLC-UV Method in the Raw Materials of Some Representatives of the Genus <i>Rumex</i> of Three Vegetation Time
Introduction. The study of the dynamics of accumulation of biologically active substances (hereinafter – BAS) in relation to the phonological phases of plant development is of great scientific and practical interest. The quantitative content of aglycones and glycosides of flavonoids depends on the life cycle of the plant and its vegetation phase. Aim. To identify and quantify flavonoids in the underground organs of Rumex confertus Willd., Rumex aquaticus L., Rumex crispus L. and Rumex obtusifolius L. harvested during different phases of vegetation. Materials and methods. Extracts from the underground organs of the studied plants, obtained according to the method from the pharmacopoeial article on R. confertus , were analyzed. Chromatographic separation and detection were performed on a Nexera-i LC-2040 high-performance liquid chromatograph (Shimadzu Corporation, Japan). The chromatograph was equipped with a column thermostat, chromatography column Grace HPLC-COLUMN 250 × 4.6mm platinum C8-EPS 5 mm (Grace, США) and Guard column Phenomenex SecurityGuard TM Cartridges Widepore C18 4 × 3,0 mm, a degasser, an autosampler (injection volume: 10 µl), and an ultraviolet detector. Detection was carried out at a wavelength λ = 365 ± 2 nm. Mobile phase contains 0.1 % phosphoric acid in water (v/v) (eluent A); acetonitrile (eluent B) with flow rate: 0.9 ml/min. Results and discussion. All studied objects were analyzed. The authenticity of the substances contained were confirmed using the external standard, and their quantitative content was determined. The discovered and quantified substances were: 3-O-rutinoside of quercetin (rutin), 3-O-rutinoside of isorhamnetin (narcissin), 3-O-glucoside of kaempferol (astragalin), luteolin, kaempferol and isorhamnetin. 7-O-glucoside of luteolin (cynaroside) and 7-O-beta-D-glucoside apigenin (cosmosiin) were not found. The aglycone luteolin had the biggest share in the total quantitative content of flavonoids. It is noted that this aglycone is contained in larger quantities in relation to other flavonoids in all studied objects, regardless of the phase of vegetation. Conclusion. In the process of the research, a method for the quantitative determination of flavonoids in alcohol-water extracts was developed. Aglycones and glycosides of flavonoids were identified and quantified in the underground organs of R. confertus Willd., R. aquaticus L., R. crispus L. and R. obtusifolius L. of three different vegetations.
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来源期刊
Drug Development and Registration
Drug Development and Registration Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
1.20
自引率
0.00%
发文量
61
审稿时长
8 weeks
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