Identification and quantification of flavonoids in medicinal plants growing in the Republic of Uzbekistan

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Introduction. In recent years, the popularity of herbal medicine has been increasing. One of the most numerous classes of biologically active substances of plant origin are flavonoids, which have a wide range of biological activities: anticarcinogenic, antioxidant, antimicrobial, neuroprotective, immunomodulatory, hepatoprotective effects, and also capable of stimulating the damaged body tissues regeneration processes. The relevant area of the research is the search for medicinal plants with a high content of flavonoids for the development of herbal remedies with wound-healing activity. This problem can be solved through the use of plant raw materials from the Republic of Uzbekistan, which have a high content and a wide range of biologically active substances, thanks to the sharply continental climate of the country with consistently hot summers and increased levels of ultraviolet radiation.

The purpose of the research is to select medicinal plant raw materials as a source of flavonoids for the development of wound healing agents.

Material and methods. The object of the study was medicinal plant raw materials harvested on the territory of the Republic of Uzbekistan: oregano herb, sage leaves, St. John's wort herb, sandy everlasting flowers, bur beggar-ticks herb. Identification and quantification of flavonoids in the studied samples of medicinal plants was carried out using thin-layer chromatography, absorption spectrophotometry in the visible region using reaction with aluminum chloride and high-performance liquid chromatography-mass spectrometry.

Results. It has been established that the content of flavonoids in the herb of oregano, leaves of medicinal sage, St. John's wort herb, flowers of sandy everlasting, harvested in the Republic of Uzbekistan, is significantly higher than in medicinal plant materials harvested in the territory of the Republic of Belarus and the Russian Federation. Using the method of thin-layer chromatography and high-performance liquid chromatography-mass spectrometry, kaempferol-3-β-D-glucopyranoside was identified in the extract of sandy everlasting flowers, and isoquercitrin was identified in the extract of St. John's wort herb.

Conclusions. As a result of the research, sandy everlasting and St. John's wort, growing on the territory of the Republic of Uzbekistan, were selected as the sources of flavonoids (glycoside kaempferol and isoquercitrin) with regenerating properties for the development of wound healing agents.

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作者简介

V. Leontiev

Belarusian State Technological University

编辑信件的主要联系方式.
Email: chernetskaya@belstu.by

Ph.D. (Chem.), Head of the Department of Biotechnology

白俄罗斯, Minsk

О. Ignatovets

Belarusian State Technological University

Email: chernetskaya@belstu.by

Ph.D. (Biol.), Associate Professor

白俄罗斯, Minsk

A. Feskova

Belarusian State Technological University

Email: chernetskaya@belstu.by

Ph.D. (Eng.), Senior Researcher, Department of Biotechnology

白俄罗斯, Minsk

Yu. Charnetskaya

Belarusian State Technological University

Email: chernetskaya@belstu.by

Ph.D. (Pharm.), Associate Professor, Department of Biotechnology

白俄罗斯, Minsk

N. Adamtsevich

Belarusian State Technological University

Email: chernetskaya@belstu.by

Ph.D. (Biol.), Senior lecturer, Department of Biotechnology

白俄罗斯, Minsk

Ya. Strakh

Belarusian State Technological University

Email: chernetskaya@belstu.by

Assistant, Department of Biotechnology

白俄罗斯, Minsk

D. Mirzarakhmetova

Tashkent International Kimyo University

Email: chernetskaya@belstu.by

Dr.Sc. (Eng.), Professor, Department of "Chemistry and Biology"

乌兹别克斯坦, Tashkent

参考

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2. Fig. 1. Chromatogram of sandy everlasting flower extract

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3. Fig. 2. Mass spectrum of a compound with a retention time of 10.76 min: а – region of positive ions; б – region of negative ions

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4. Fig. 3. Electronic spectrum of the substance with a retention time of 10.76 min

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5. Fig. 4. Chromatogram of St. John's wort herb extract

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6. Fig. 5. Mass spectrum of the compound with a retention time of 13.34 min: а – region of positive ions; б – region of negative ions

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