Sturm Sonja, Seger Christoph, Godejohann Markus, Spraul Manfred, Stuppner Hermann
Institute of Pharmacy/Pharmacognosy, Center of Molecular Biosciences, Leopold Franzens University Innsbruck, Innrain 52, A-6020 Innsbruck, Austria.
J Chromatogr A. 2007 Sep 7;1163(1-2):138-44. doi: 10.1016/j.chroma.2007.06.029. Epub 2007 Jun 23.
Identification of putative biomarker molecules within the genus Corydalis (Papaveraceae) was pursued by combining conventional off-line sample enrichment with high-performance liquid chromatography-solid phase extraction-nuclear magnetic resonance (HPLC-SPE-NMR) based structure elucidation. Off-line reversed phase solid phase extraction (SPE) was used to enrich the desired analytes from a methanolic extract (93 mg dry weight) of a miniscule single tuber (233 mg dry weight) of C. solida. An aliquot of the SPE fraction (2.1 mg) was subjected to separation in the HPLC-SPE-NMR hyphenation. Chromatographic peaks bearing the metabolites under investigation were trapped in the SPE device in a single experiment and transferred to a 600 MHz NMR spectrometer equipped with a 30 microl cryofit insert fed into a 3 mm cryoprobe. Recorded homo- and heteronuclear 1D and 2D NMR data allowed the identification of the three analytes under investigation as protopine, allocryptopine, and N-methyl-laudanidinium acetate. The latter is a rare alkaloid, which has been isolated only once before.
通过将传统的离线样品富集与基于高效液相色谱 - 固相萃取 - 核磁共振(HPLC - SPE - NMR)的结构解析相结合,在紫堇属(罂粟科)中寻找假定的生物标志物分子。离线反相固相萃取(SPE)用于从极小的单块块茎(干重233毫克)的C. solida甲醇提取物(干重93毫克)中富集所需分析物。将SPE馏分的等分试样(2.1毫克)进行HPLC - SPE - NMR联用分离。在单个实验中,将含有所研究代谢物的色谱峰捕获在SPE装置中,并转移到配备有30微升低温适配插入物的600 MHz核磁共振光谱仪中,该插入物连接到3毫米低温探头。记录的同核和异核一维和二维NMR数据使得能够鉴定所研究的三种分析物为原阿片碱、别隐品碱和乙酸N - 甲基劳丹定𬭩。后者是一种罕见的生物碱,之前仅被分离过一次。