| Literature DB >> 21494318 |
Yi Yang1, Yongxin Zhao, Dongyu Gu, Amatjan Ayupbek, Yun Huang, Jun Dou, Yoichiro Ito, Tianyou Zhang, Haji Akber Aisa.
Abstract
An effective high-speed countercurrent chromatography (HSCCC) method was established for further separation and purification of four minor flavonols in addition to five major flavonols which were reported by our previous study from extracts of Flos Gossypii. HSCCC was performed with three two-phase solvent systems composed of n-hexane-ethyl acetate-methanol-water (7.5:15:6:7, v/v), (2.5:15:2:7, v/v) and (0:1:0:1, v/v). The separation was repeated 3 times, and 3.8 mg of 8-methoxyl-kaempferol-7-O-β-D-rhamnoside (HPLC purity 98.27%), 6.7 mg of astragalin (HPLC purity 94.18%), 3.3 mg of 4'-methoxyl-quercetin-7-O-β-D-glucoside (HPLC purity 94.30%) and 8.2 mg of hyperoside (HPLC purity 93.48%) were separated from 150 mg of the crude sample. The chemical structures of the flavonols were confirmed by MS, (1)H NMR and (13)C NMR. Meanwhile, the results indicated that the target compound with smaller K value (<0.5) can be separated by increasing column length of HSCCC. And four separation rules of flavonols according to the present study and references were summarized, which can be used as a useful guide for separation of flavonols by HSCCC.Entities:
Year: 2010 PMID: 21494318 PMCID: PMC3008776 DOI: 10.1080/10826076.2010.489000
Source DB: PubMed Journal: J Liq Chromatogr Relat Technol ISSN: 1082-6076 Impact factor: 1.312