Affiliation:
1. College of Pharmacy Shandong University of Traditional Chinese Medicine Jinan P. R. China
2. Medicine and Food R&D and Health Product Creation International Joint Laboratory Biological Engineering Technology Innovation Center of Shandong Province Heze Branch of Qilu University of Technology (Shandong Academy of Sciences) Heze P. R. China
3. Liaocheng Agro Technical Extension and Service Center of Shandong Province Liaocheng P. R. China
4. Department of Genetics and Cell Biology Basic Medical College Qingdao University Qingdao P. R. China
5. Department of Reproductive Medicine the Affiliated Hospital of Qingdao University Qingdao P. R. China
Abstract
Tubers of Gymnadenia conopsea (L.) R. Br. (Orchidaceae), a traditional medicine and food homologous plant, has a broad application and development prospect in the food and drug industries. Benzylester glucosides, the main effective active components in this plant, are difficult to separate due to their similar structures and high polarity. In this study, linear gradient counter‐current chromatography was used to separate benzylester glucosides and derivatives, combined with elution‐extrusion mode. The main separation parameters were optimized, including the ratio of mobile phase and sample loading. Finally, seven compounds were successfully separated, including 4‐hydroxybenzyl alcohol (1), 4‐hydroxybenzaldehyde (2), dactylorhin B (3), loroglossin (4), dactylorhin A (5), 4‐(ethoxymethyl) phenol (6), and militarine (7). The structures were analyzed by mass spectrometry and nuclear magnetic resonance spectrometry. According to our findings, the established method was an efficient approach to separate benzylester glucosides and derivatives from tubers of G. conopsea. The established strategy could be applied to purify other similar high‐polarity compounds from complex natural products.
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