| Literature DB >> 29291840 |
Li Zhang1, Hong Shen2, Jun Xu3, Jin-Di Xu4, Zhen-Ling Li4, Jie Wu4, Ye-Ting Zou2, Li-Fang Liu5, Song-Lin Li6.
Abstract
In this study, a novel ultra-performance liquid chromatography coupled with quadrupole/time-of-flight mass spectrometry (UPLC-QTOF-MS/MS)-guidance strategy was proposed for preparation of sulfur-containing derivatives in sulfur-fumigated edible herbs. Being versatile in both chromatographic separation and mass spectrometric detection, UPLC-QTOF-MS/MS was inducted into each experimental step for multifaceted purposes including finding, tracking, purity determination and structural elucidation of targeted compounds as well as UPLC-HPLC chromatographic conditions transplantation, whereby the isolation and purification procedures were greatly facilitated. Using this strategy, a new sulfur-containing ginsenoside Rg1 derivative (named compound I) was obtained from sulfur-fumigated ginseng. The chemical structure of compound I was elucidated to be (3β, 6α, 12β)-3, 12-dihydroxydammar-25-ene-6, 20-diylbis-β-d-glucopyranoside, 24-sulfonic acid by QTOF-MS/MS, 1H-NMR and 13C-NMR analysis, and its generation mechanisms by sulfur-fumigation were accordingly discussed. The research deliverable suggests that the UPLC-QTOF-MS/MS-guidance strategy is promising for targeted preparation of sulfur-containing derivatives from sulfur-fumigated edible herbs.Entities:
Keywords: Ginsenoside Rg(1); Isolation and purification; Sulfur-containing derivatives; Sulfur-fumigated ginseng; UPLC-QTOF-MS/MS
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Year: 2017 PMID: 29291840 DOI: 10.1016/j.foodchem.2017.10.151
Source DB: PubMed Journal: Food Chem ISSN: 0308-8146 Impact factor: 7.514