Yang Yi, Zhao Yongxin, Gu Dongyu, Ayupbek Amatjan, Huang Yun, Dou Jun, Ito Yoichiro, Zhang Tianyou, Aisa Haji Akber
Xinjiang Key Laboratory of Plant Resources and Natural Products Chemistry, Xinjiang Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Urumqi 830011, China.
J Liq Chromatogr Relat Technol. 2010 Jan 1;33(16):1502-1515. doi: 10.1080/10826076.2010.489000.
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.
建立了一种有效的高速逆流色谱(HSCCC)方法,用于进一步分离和纯化除了本课题组前期从棉花花提取物中报道的5种主要黄酮醇之外的4种次要黄酮醇。HSCCC采用由正己烷-乙酸乙酯-甲醇-水(7.5:15:6:7,v/v)、(2.5:15:2:7,v/v)和(0:1:0:1,v/v)组成的3种两相溶剂系统进行。分离重复3次,从150 mg粗样品中分离得到3.8 mg的8-甲氧基山奈酚-7-O-β-D-鼠李糖苷(HPLC纯度98.27%)、6.7 mg的紫云英苷(HPLC纯度94.18%)、3.3 mg的4'-甲氧基槲皮素-7-O-β-D-葡萄糖苷(HPLC纯度94.30%)和8.2 mg的金丝桃苷(HPLC纯度93.48%)。通过质谱、氢核磁共振谱和碳核磁共振谱对黄酮醇的化学结构进行了确证。同时,结果表明K值较小(<0.5)的目标化合物可通过增加HSCCC柱长进行分离。并总结了根据本研究及参考文献得到的黄酮醇的4条分离规律,可作为HSCCC分离黄酮醇的有用指导。