Plant Protection Institute, Centre for Agricultural Research, ELKH, Herman O. Str. 15, 1022 Budapest, Hungary.
Plant Protection Institute, Centre for Agricultural Research, ELKH, Herman O. Str. 15, 1022 Budapest, Hungary.
J Chromatogr B Analyt Technol Biomed Life Sci. 2021 Nov 15;1185:123004. doi: 10.1016/j.jchromb.2021.123004. Epub 2021 Oct 21.
Eight bioactive clerodane diterpenes from the root extract of Solidago gigantea Ait. (giant goldenrod) were quantified by high-performance thin-layer chromatography (HPTLC) and two newly developed hyphenated methods. One uses vanillin sulphuric acid derivatization and densitometry, and the other an inhibition assay of acetylcholinesterase (AChE) and video densitometry. Both methods gave figures of merit for quantification including 5.8-33.9 ng and 175.5-448.7 ng LOQs and 2.7-6.9 RSD% and 8.8-13.9 RSD% inter-day precisions, respectively. Based on the diterpenes' content of 14 root samples collected over a year from the same plant population, the fully flowering plant is suggested to collect the root as a source of these compounds. Excepting one diterpene (with the lowest retardation factor), the quantitative results for the richest sample obtained by the two methods were in harmony. The difference could be due to a matrix effect.
从巨型一枝黄花(giant goldenrod)根提取物中分离得到了 8 种生物活性的 clerodane 二萜,并通过高效薄层色谱(HPTLC)和两种新开发的联用方法进行了定量分析。一种方法使用香草醛硫酸衍生化和密度测定法,另一种方法则是乙酰胆碱酯酶(AChE)抑制测定法和视频密度测定法。这两种方法都给出了定量的优良指标,包括 5.8-33.9ng 和 175.5-448.7ng 的 LOQs,以及 2.7-6.9%和 8.8-13.9%的日间精密度 RSD。基于对同一植物种群中一年中采集的 14 个根样本的二萜含量的分析,建议在植物完全开花时采集根作为这些化合物的来源。除了一种(具有最低保留因子)二萜外,两种方法中获得的最丰富样本的定量结果是一致的。差异可能是由于基质效应所致。