Institute of Pharmacy, Pharmacognosy, Center for Molecular Biosciences (CMBI), University of Innsbruck, Innrain 80-82, Innsbruck 6020, Austria.
Institute of Pharmacy, Pharmacognosy, Center for Molecular Biosciences (CMBI), University of Innsbruck, Innrain 80-82, Innsbruck 6020, Austria.
J Chromatogr A. 2024 Nov 22;1737:465432. doi: 10.1016/j.chroma.2024.465432. Epub 2024 Oct 10.
Anthraquinones are the major bioactive compounds in alder buckthorn, a plant with a long history of use for the treatment of obstipation in European and Asian traditional medicine. As these metabolites are also associated with toxic side effects, reliable analytical techniques for their determination are essential. Previously described methods mainly utilized Liquid Chromatography for this purpose, as the photometric assay described in the current edition of the European Pharmacopoeia lacks selectivity. In this study, the development and application of an alternative approach, Ultra-High Performance Supercritical Fluid Chromatography, is presented, facilitating the qualitative and quantitative determination of seven anthraquinone derivatives in under six minutes. This was possible by using a Torus™ DIOL column and a modifier comprising methanol with 10 % acetonitrile and 2.5 mM oxalic acid; applying a flow rate of 1.6 mL/min and an elevated temperature of 55 °C enabled optimal resolution. Regarding selectivity, linearity (R ≥ 0.9995), precision and accuracy (recovery rates between 96.6 and 103.3 %), all results were in line with the respective ICH requirements. Practical applicability of the assay was confirmed by analyzing different samples, including commercially available plant material, phytopharmaceuticals containing Frangula bark and wild collected samples. Except of the latter, glucofrangulin A always was the dominating compound; however, the overall anthraquinone content showed to be very variable ranging from 2.18 to 51.32 mg.
蒽醌类化合物是樗榆的主要生物活性化合物,樗榆在欧洲和亚洲传统医学中被广泛用于治疗便秘已有很长的历史。由于这些代谢物也与毒性副作用有关,因此需要可靠的分析技术来确定它们的含量。以前描述的方法主要使用液相色谱法,因为当前版欧洲药典中描述的分光光度法缺乏选择性。在这项研究中,提出了一种替代方法,即超高效超临界流体色谱法的开发和应用,该方法可在不到六分钟的时间内定性和定量测定七种蒽醌衍生物。这是通过使用 Torus™ DIOL 柱和包含甲醇、10%乙腈和 2.5 mM 草酸的改性剂来实现的;以 1.6 mL/min 的流速和 55°C 的高温应用,可实现最佳分辨率。关于选择性、线性(R ≥ 0.9995)、精密度和准确度(回收率在 96.6%至 103.3%之间),所有结果均符合相应的 ICH 要求。通过分析不同的样品,包括市售植物材料、含有鼠李皮的植物药和野生采集的样品,验证了该方法的实际应用。除了后者,葡萄糖呋喃素 A 总是占主导地位的化合物;然而,蒽醌的总含量变化很大,范围从 2.18 到 51.32 毫克。