Chair of Food Science, Institute of Nutritional Science, Interdisciplinary Research Center (IFZ), Justus Liebig University Giessen, Heinrich-Buff-Ring 26-32, 35392, Giessen, Germany.
J Chromatogr A. 2018 Jan 19;1533:180-192. doi: 10.1016/j.chroma.2017.12.014. Epub 2017 Dec 6.
An affordable bioanalytical workflow supports the collection of data on active ingredients, required for the understanding of health-related food, superfood and traditional medicines. Targeted effect-directed responses of single compounds in a complex sample highlight this powerful bioanalytical hyphenation of planar chromatography with (bio)assays. Among many reports about biological properties of Salvia miltiorrhiza Bunge root (Danshen) and their analytical methods, the highly efficient direct bioautography (DB) workflow has not been considered so far. There was just one TLC-acetylcholinesterase (AChE) method with a poor zone resolution apart from our two HPTLC-DB studies, however, all methods were focused on the nonpolar extracts of Danshen (tanshinones) only. The current study on HPTLC-UV/Vis/FLD-(bio)assay-HRMS, followed by streamlined scale-up to preparative layer chromatography (PLC)-H-NMR, aimed at an even more streamlined, yet comprehensive bioanalytical workflow. It comprised effect-directed screening of both, its polar (containing phenolics) and nonpolar extracts (containing tanshinones) on the same HPTLC plate, the biochemical and biological profiling with four different (bio)assays and elucidation of structures of known and unidentified active compounds. The five AChE inhibitors, salvianolic acid B (SAB), lithiospermic acid (LSA) and rosmarinic acid (RA) as well as cryptotanshinone (CT) and 15,16-dihydrotanshinone I (DHTI) were confirmed, but also unidentified inhibitors were observed. In the polar extracts, SAB, LSA and RA exhibited free radical scavenging properties in the 2,2-diphenyl-1-picrylhydrazyl assay. CT, DHTI and some unidentified nonpolar compounds were found active against Gram-positive Bacillus subtilis and Gram-negative Aliivibrio fischeri (LOD 12 ng/band for CT, and 5 ng/band for DHTI). For the first time, the most multipotent unidentified active compound zone in the B. subtilis, A. fischeri and AChE fingerprints of the nonpolar Danshen extract was identified as co-eluted band of 1,2-dihydrotanshinone and methylenetanshinquinone in the ratio of 2:1.
一种经济实惠的生物分析工作流程支持收集活性成分的数据,这对于理解与健康相关的食品、超级食品和传统药物是必要的。在复杂样品中,靶向的、有针对性的直接活性导向分析(DB)对平面色谱与(生物)分析的这种强大的生物分析连接具有突出作用。在许多关于丹参(Danshen)根及其分析方法的生物学特性的报告中,迄今为止,高效直接生物自显影(DB)工作流程尚未得到考虑。除了我们的两项 HPTLC-DB 研究外,只有一项 TLC-乙酰胆碱酯酶(AChE)方法具有较差的区域分辨率,但所有方法都仅专注于丹参的非极性提取物(丹参酮)。目前,在 HPTLC-UV/Vis/FLD-(生物)分析-HRMS 之后,通过简化的规模扩大到制备层色谱(PLC)-H-NMR,旨在实现更简化但全面的生物分析工作流程。它包括在同一 HPTLC 板上对极性(含有酚类)和非极性提取物(含有丹参酮)进行定向活性筛选,使用四种不同的(生物)分析进行生物化学和生物特征分析,并阐明已知和未知活性化合物的结构。确认了五种 AChE 抑制剂,丹酚酸 B(SAB)、迷迭香酸(LSA)和迷迭香酸(RA)以及隐丹参酮(CT)和 15,16-二氢丹参酮 I(DHTI),但也观察到了未鉴定的抑制剂。在极性提取物中,SAB、LSA 和 RA 在 2,2-二苯基-1-苦基肼测定中表现出自由基清除特性。CT、DHTI 和一些未鉴定的非极性化合物对革兰氏阳性枯草芽孢杆菌和革兰氏阴性发光弧菌(CT 的 LOD 为 12ng/带,DHTI 的 LOD 为 5ng/带)具有活性。首次在非极性丹参提取物的 B. subtilis、A. fischeri 和 AChE 指纹图谱中鉴定出最具多效性的未鉴定活性化合物区带为 1,2-二氢丹参酮和亚甲基丹参醌的共洗脱带,比例为 2:1。