Babili Fatiha El, Fouraste I, Rougaignon C, Moulis C, Chatelain C
UMR 5623 - Faculté des Sciences Pharmaceutiques de Toulouse, Laboratoire de Botanique-Mycologie, Faculté de Pharmacie, 35 ch. des Maraîchers - F- 31062 Toulouse, France.
Pharmacogn Mag. 2012 Apr;8(30):175-80. doi: 10.4103/0973-1296.96587.
A botanical study is conducted to provide a standard diagnostic tool. In order to improve the quality assurance of the secondary tuberized roots of Harpagophytum procumbens, derived extract and phytomedicine, a simple, rapid, and accurate high-performance liquid chromatography (HPLC) method was developed to assess the harpagoside. MATERIAL AND MEHODS: This HPLC assay was performed on a reversedphase C18 column with methanol and water (50/50-V/V) as the mobile phase with a flow rate of 1.5 mL/min and using a monitoring wavelength at 278 nm.
This method was successfully applied to quantify these bioactive iridoid in an aqueous extract of H. procumbens and in its related phytomedicine "harpagophyton". The result demonstrated that the quantification of harpagoside, indicating that the quality control of the bioactive ingredient in H. procumbens, derived extract and phytomedicine, is critical to ensure its clinical benefits.
开展一项植物学研究以提供一种标准诊断工具。为提高南非钩麻二次块根、提取物及植物药的质量保证,开发了一种简单、快速且准确的高效液相色谱(HPLC)法来测定哈帕苷。材料与方法:该HPLC分析在反相C18柱上进行,以甲醇和水(50/50 - V/V)作为流动相,流速为1.5 mL/min,监测波长为278 nm。
该方法成功应用于定量南非钩麻水提取物及其相关植物药“钩麻”中的这些生物活性环烯醚萜。结果表明,哈帕苷的定量表明,对南非钩麻、提取物及植物药中生物活性成分的质量控制对于确保其临床益处至关重要。