An efficient and target-oriented sample enrichment method for preparative separation of minor alkaloids by pH-zone-refining counter-current chromatography

• Published in: Journal of Chromatography A Vol. 1409; pp. 159 - 165
• Main Authors: Feng, Rui-Hong, Hou, Jin-Jun, Zhang, Yi-Bei, Pan, Hui-Qin, Yang, Wenzhi, Qi, Peng, Yao, Shuai, Cai, Lu-Ying, Yang, Min, Jiang, Bao-hong, Liu, Xuan, Wu, Wan-Ying, Guo, De-An
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 28.08.2015
• Subjects: Acetates; Chromatography, High Pressure Liquid - methods; Countercurrent Distribution - methods; Hexanes; Hydrogen-Ion Concentration; Indole alkaloids; Indole Alkaloids - isolation & purification; Methanol; pH-zone-refining counter-current chromatography; Plant Extracts - chemistry; Solvents; Target-oriented sample enrichment method; Uncaria - chemistry; Uncaria rhynchophylla; pH-zone-refining counter-current chromatography; Indole alkaloids; Uncaria rhynchophylla; Target-oriented sample enrichment method
• ISSN: 0021-9673; 1873-3778
• DOI: 10.1016/j.chroma.2015.07.066

•Developed a sample enrichment method focusing on the target minor alkaloids.•High transfer rate and specification were shown for the method.•Very suitable for sample pretreatment of pH-zone-refining CCC.•Seven minor indole alkaloids in Uncaria rhynchophylla were first simultaneously separated by the method. An efficient and target-oriented sample enrichment method was established to increase the content of the minor alkaloids in crude extract by using the corresponding two-phase solvent system applied in pH-zone-refining counter-current chromatography. The enrichment and separation of seven minor indole alkaloids from Uncaria rhynchophylla (Miq.) Miq. ex Havil(UR) were selected as an example to show the advantage of this method. An optimized two-phase solvent system composed of n-hexane-ethyl acetate-methanol-water (3:7:1:9, v/v) was used in this study, where triethylamine (TEA) as the retainer and hydrochloric acid (HCl) as the eluter were added at the equimolar of 10mM. Crude alkaloids of UR dissolved in the corresponding upper phase (containing 10mM TEA) were extracted twice with lower phase (containing 10mM TEA) and lower phase (containing 10mM HCl), respectively, the second lower phase extract was subjected to pH-zone-refining CCC separation after alkalization and desalination. Finally, from 10g of crude alkaloids, 4g of refined alkaloids was obtained and the total content of seven target indole alkaloids was increased from 4.64% to 15.78%. Seven indole alkaloids, including 54mg isocorynoxeine, 21mg corynoxeine, 46mg isorhynchophylline, 35mg rhynchophylline, 65mg hirsutine, 51mg hirsuteine and 27mg geissoschizine methylether were all simultaneously separated from 2.5g of refined alkaloids, with the purity of 86.4%, 97.5%, 90.3%, 92.1%, 98.5%, 92.3%, and 92.8%, respectively. The total content and purities of the seven minor indole alkaloids were tested by HPLC and their chemical structures were elucidated by ESI-HRMS and 1H NMR.