N. Antonova, E. Shefer, N. E. Semenova, A. Kalinin, S. S. Prokhvatilova, I. M. Morgunov
{"title":"Application of HPLC for Evaluation and Standardisation of Hawthorn Flower Herbal Substance","authors":"N. Antonova, E. Shefer, N. E. Semenova, A. Kalinin, S. S. Prokhvatilova, I. M. Morgunov","doi":"10.30895/1991-2919-2019-9-3-177-183","DOIUrl":null,"url":null,"abstract":"The process of harmonisation of Russian and foreign approaches and requirements in the field of medicines quality assurance calls for revision of quality control procedures included in various regulations and guidelines. The monograph FS.2.5.0062.18 “Hawthorn flowers” of the State Pharmacopoeia of the Russian Federation XIV edition includes a test procedure for determination of flavonoids by a chromatospectrophotometric method. This procedure does not take into account current scientific capabilities and has a number of shortcomings, therefore it was necessary to revise the existing test procedure and develop a new approach to the standardisation of the hawthorn flower herbal substance.The objectiveof the studywas to develop an assay method for standardisation and evaluation of hawthorn flower using high performance liquid chromatography (HPLC).Materials and methods:the study was performed using samples of hawthorn flowers by Russian manufacturers. Quercetin (USP RS) and Hyperoside (HWI, primary standard) were used as the reference standards. The HPLC analysis was performed using an Infinity II 1260 DAD LC system (Agilent), and the UV spectra were recorded on a Cary 100 Varian spectrophotometer. A TLC Visualizer (CAMAG) was used to obtain digital images of thin layer chromatography plates.Results:the authors developed an HPLC test procedure for quantitative determination of total flavonoids, expressed as hyperoside, in hawthorn flowers. The developed procedure gives reliable and reproducible results and is characterised by high sensitivity and selectivity. The results of quantitative determination of the total flavonoid content in hawthorn flowers were used to propose the standard for the total content of flavonoids, expressed as hyperoside, of “not less than 0.5%”.Conclusions:the developed assay method for determination of active pharmaceutical ingredients in hawthorn flower products by HPLC can be recommended for inclusion into the Assay part of the “Hawthorn Flowers” monograph of the State Pharmacopoeia of the Russian Federation.","PeriodicalId":22286,"journal":{"name":"The Bulletin of the Scientific Centre for Expert Evaluation of Medicinal Products","volume":"27 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2019-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Bulletin of the Scientific Centre for Expert Evaluation of Medicinal Products","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.30895/1991-2919-2019-9-3-177-183","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
The process of harmonisation of Russian and foreign approaches and requirements in the field of medicines quality assurance calls for revision of quality control procedures included in various regulations and guidelines. The monograph FS.2.5.0062.18 “Hawthorn flowers” of the State Pharmacopoeia of the Russian Federation XIV edition includes a test procedure for determination of flavonoids by a chromatospectrophotometric method. This procedure does not take into account current scientific capabilities and has a number of shortcomings, therefore it was necessary to revise the existing test procedure and develop a new approach to the standardisation of the hawthorn flower herbal substance.The objectiveof the studywas to develop an assay method for standardisation and evaluation of hawthorn flower using high performance liquid chromatography (HPLC).Materials and methods:the study was performed using samples of hawthorn flowers by Russian manufacturers. Quercetin (USP RS) and Hyperoside (HWI, primary standard) were used as the reference standards. The HPLC analysis was performed using an Infinity II 1260 DAD LC system (Agilent), and the UV spectra were recorded on a Cary 100 Varian spectrophotometer. A TLC Visualizer (CAMAG) was used to obtain digital images of thin layer chromatography plates.Results:the authors developed an HPLC test procedure for quantitative determination of total flavonoids, expressed as hyperoside, in hawthorn flowers. The developed procedure gives reliable and reproducible results and is characterised by high sensitivity and selectivity. The results of quantitative determination of the total flavonoid content in hawthorn flowers were used to propose the standard for the total content of flavonoids, expressed as hyperoside, of “not less than 0.5%”.Conclusions:the developed assay method for determination of active pharmaceutical ingredients in hawthorn flower products by HPLC can be recommended for inclusion into the Assay part of the “Hawthorn Flowers” monograph of the State Pharmacopoeia of the Russian Federation.
在药品质量保证领域协调俄罗斯和外国方法和要求的过程要求修订各种法规和指南中包含的质量控制程序。俄罗斯联邦国家药典第十四版专著FS.2.5.0062.18“山楂花”包括用色谱分光光度法测定黄酮类化合物的测试程序。该程序没有考虑到当前的科学能力,并且有许多缺点,因此有必要修改现有的测试程序并开发一种新的方法来标准化山楂花草药物质。建立了一种高效液相色谱法测定山楂花质量的方法。材料与方法:采用俄罗斯厂家山楂花样品进行研究。以槲皮素(USP RS)和金丝桃苷(HWI,一级标准品)为对照品。HPLC分析采用Infinity II 1260 DAD LC系统(Agilent),紫外光谱记录在Cary 100 Varian分光光度计上。采用TLC可视化仪(CAMAG)获得薄层色谱板的数字图像。结果:建立了测定山楂花中金丝桃苷总黄酮含量的高效液相色谱方法。该方法结果可靠,重现性好,灵敏度高,选择性好。利用山楂花中总黄酮含量的定量测定结果,提出了山楂花中总黄酮含量“不低于0.5%”的标准,以金丝桃苷表示。结论:所建立的高效液相色谱法测定山楂花制品中有效药物成分的方法可推荐纳入俄罗斯联邦国家药典《山楂花》专著的测定部分。