Development of a liquid chromatography method for the analysis of oil extract of artemisia cina

Introduction. The problem of development and implementation of own drugs in Kazakhstan today is acute and urgent. The solution to this problem is possible through the use of own resources – domestic medicinal plant raw materials. A promising medicinal raw material is Artemisia cina – an endemic medi...

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Main Authors: S. K. Ordabayeva, A. D. Serikbayeva, H. S. Farshad, G. Bakhytkyzy
Format: Article
Language:Russian
Published: LLC Center of Pharmaceutical Analytics (LLC «CPHA») 2024-11-01
Series:Разработка и регистрация лекарственных средств
Subjects:
Online Access:https://www.pharmjournal.ru/jour/article/view/1959
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author S. K. Ordabayeva
A. D. Serikbayeva
H. S. Farshad
G. Bakhytkyzy
author_facet S. K. Ordabayeva
A. D. Serikbayeva
H. S. Farshad
G. Bakhytkyzy
author_sort S. K. Ordabayeva
collection DOAJ
description Introduction. The problem of development and implementation of own drugs in Kazakhstan today is acute and urgent. The solution to this problem is possible through the use of own resources – domestic medicinal plant raw materials. A promising medicinal raw material is Artemisia cina – an endemic medicinal plant of the of the Turkestan region of Kazakhstan.Aim. Designing a liquid chromatography methodology to analyze the oil extract obtained from Artemisia cina.Materials and methods. Standard sample (SS) of santonin, Artemisia cina’s oil extract. The substance was identified and quantitatively determined using an Agilent Technologies 1200 liquid chromatograph (USA) equipped with ChemStation software.Results and discussion. The main active substance of the oil extract was analyzed using high-performance liquid chromatography (HPLC) method. Choosing the separation conditions for the column involves determining the best composition of the mobile phase and the rate of elution. There were used a reversed-phase system with sorbent C18 and a mobile phase consisting of acetonitrile and a phosphate buffer with a pH of 6.8. Chromatographic studies of the substance were carried out in a gradient mode at an analytical wavelength of 237 nm. The retention time of the standard sample (SS) of santonin matched the retention time (tR) of santonin isolated from the oil extract of Artemisia cina and amounted to 14.3 minutes.Conclusion. A liquid chromatography method has been established for the identification and quantitative determination of the oil extract, focusing on the main active substance, santonin.
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institution Kabale University
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2658-5049
language Russian
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series Разработка и регистрация лекарственных средств
spelling doaj-art-ebe7c4f240124311bbe4a2e7700287822025-08-20T03:59:04ZrusLLC Center of Pharmaceutical Analytics (LLC «CPHA»)Разработка и регистрация лекарственных средств2305-20662658-50492024-11-0113413914710.33380/2305-2066-2024-13-4-17281294Development of a liquid chromatography method for the analysis of oil extract of artemisia cinaS. K. Ordabayeva0A. D. Serikbayeva1H. S. Farshad2G. Bakhytkyzy3JSC "South Kazakhstan Medical Academy"JSC "South Kazakhstan Medical Academy"Shahid Beheshti Medical University, School of Pharmacy, Department of pharmaceutical and toxicological chemistryJSC "South Kazakhstan Medical Academy"Introduction. The problem of development and implementation of own drugs in Kazakhstan today is acute and urgent. The solution to this problem is possible through the use of own resources – domestic medicinal plant raw materials. A promising medicinal raw material is Artemisia cina – an endemic medicinal plant of the of the Turkestan region of Kazakhstan.Aim. Designing a liquid chromatography methodology to analyze the oil extract obtained from Artemisia cina.Materials and methods. Standard sample (SS) of santonin, Artemisia cina’s oil extract. The substance was identified and quantitatively determined using an Agilent Technologies 1200 liquid chromatograph (USA) equipped with ChemStation software.Results and discussion. The main active substance of the oil extract was analyzed using high-performance liquid chromatography (HPLC) method. Choosing the separation conditions for the column involves determining the best composition of the mobile phase and the rate of elution. There were used a reversed-phase system with sorbent C18 and a mobile phase consisting of acetonitrile and a phosphate buffer with a pH of 6.8. Chromatographic studies of the substance were carried out in a gradient mode at an analytical wavelength of 237 nm. The retention time of the standard sample (SS) of santonin matched the retention time (tR) of santonin isolated from the oil extract of Artemisia cina and amounted to 14.3 minutes.Conclusion. A liquid chromatography method has been established for the identification and quantitative determination of the oil extract, focusing on the main active substance, santonin.https://www.pharmjournal.ru/jour/article/view/1959oil extract of artemisia cinasantoninidentificationassayhigh-performance liquid chromatographyvalidation
spellingShingle S. K. Ordabayeva
A. D. Serikbayeva
H. S. Farshad
G. Bakhytkyzy
Development of a liquid chromatography method for the analysis of oil extract of artemisia cina
Разработка и регистрация лекарственных средств
oil extract of artemisia cina
santonin
identification
assay
high-performance liquid chromatography
validation
title Development of a liquid chromatography method for the analysis of oil extract of artemisia cina
title_full Development of a liquid chromatography method for the analysis of oil extract of artemisia cina
title_fullStr Development of a liquid chromatography method for the analysis of oil extract of artemisia cina
title_full_unstemmed Development of a liquid chromatography method for the analysis of oil extract of artemisia cina
title_short Development of a liquid chromatography method for the analysis of oil extract of artemisia cina
title_sort development of a liquid chromatography method for the analysis of oil extract of artemisia cina
topic oil extract of artemisia cina
santonin
identification
assay
high-performance liquid chromatography
validation
url https://www.pharmjournal.ru/jour/article/view/1959
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AT adserikbayeva developmentofaliquidchromatographymethodfortheanalysisofoilextractofartemisiacina
AT hsfarshad developmentofaliquidchromatographymethodfortheanalysisofoilextractofartemisiacina
AT gbakhytkyzy developmentofaliquidchromatographymethodfortheanalysisofoilextractofartemisiacina