Current Approaches to Valerian Tincture Standardisation in Terms of Assay

N. Antonova, E. Shefer, A. Kalinin, N. E. Semenova, S. S. Prokhvatilova, I. M. Morgunov
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引用次数: 1

Abstract

The quality control of the «Valerian rhizome and roots» herbal substance is carried out using high performance liquid chromatography (HPLC) according to the State Pharmacopoeia of the Russian Federation, XIV edition. The quantitative analysis of the active ingredients in valerian tincture is performed using a non-specific and non-selective spectrophotometric method. Therefore, it is important to introduce in Russia a more modern test procedure for quantitative determination of active ingredients in valerian tincture.The aim of the study was to develop a selective and sensitive HPLC procedure for quantitative determination of the total content of sesquiterpenic acids, expressed as valerenic acid, for the purpose of valerian tincture standardisation.Materials and methods: valerian tincture samples produced by seven Russian manufacturers were used as test samples, and valerenic acid was used as the reference standard. The quantitative analysis of the active ingredients was performed by two methods: spectrophotometry at 512 nm following the reaction of valerenic acid ethylester with hydroxyalamine and ferric chloride, and by HPLC using a Nucleosil C18 column, 125×4.6 mm, 5 µm particle size, in gradient elution mode, with detection at 220 nm.Results: the spectrophotometric technique was shown to be insufficiently specific. The authors of the study validated the chromatographic test procedure, established system suitability criteria, and compared the results obtained by the two test procedures. They also determined a tentative standard of the total content of sesquiterpenic acids, expressed as valerenic acid, obtained by HPLC.Conclusions: the HPLC assay developed for quantitative determination of active ingredients in valerian tincture is more specific as compared to the spectrophotometric technique, as the sum of the peaks of valerenic and acetoxyvalerenic acids and the results for the reference standard are taken into account during calculations. The new test procedure is in line with the cross-cutting standardisation principle and can be recommended for inclusion into the draft monograph «Valerian tincture».
现行缬草酊剂测定标准的方法
根据俄罗斯联邦国家药典第十四版,使用高效液相色谱(HPLC)对“缬草根茎”草药物质进行质量控制。采用非特异性、非选择性分光光度法对缬草酊剂中的有效成分进行了定量分析。因此,重要的是在俄罗斯引进一个更现代的测试程序,以定量测定缬草酊剂中的有效成分。本研究的目的是建立一种选择性和灵敏度高的高效液相色谱方法,用于定量测定缬草酊剂中倍半萜酸(以缬草酸表示)的总含量,用于缬草酊剂的标准化。材料与方法:以俄罗斯7家厂家生产的缬草酊剂样品为检测样品,以戊酸为参比标准品。有效成分的定量分析采用两种方法:一种是采用羟alamine和氯化铁与戊酸乙酯反应后的512 nm分光光度法;另一种是采用Nucleosil C18色谱柱,125×4.6 mm, 5µm粒径,梯度洗脱,220 nm检测。结果:分光光度法的特异度不够。本研究的作者验证了色谱测试程序,建立了系统适用性标准,并比较了两种测试程序获得的结果。他们还确定了用高效液相色谱法测定倍半萜烯酸总含量的暂定标准,以戊酸表示。结论:与分光光度法相比,高效液相色谱法在计算时考虑了戊酸和乙酰氧基戊酸的峰和与参比标准品的结果,使缬草酊剂中有效成分的定量测定更具特异性。新的测试程序符合交叉标准化原则,可以推荐纳入专着草案“缬草酊剂”。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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