He Dajun, Huang Yun, Ayupbek Amatjan, Gu Dongyu, Yang Yi, Aisa Haji Akber, Ito Yoichiro
Xinjiang Key Laboratory of Plant Resources and Natural Products Chemistry, Xinjiang Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Urumqi, China.
J Liq Chromatogr Relat Technol. 2010 Mar 1;33(5):615-628. doi: 10.1080/10826071003608447.
High-speed countercurrent chromatography (HSCCC) has been successfully used for the preparative isolation of flavonoids from the ethyl acetate extracts of black currant leaves. The HSCCC separation was performed with a two-phase solvent system composed of n-hexane/EtOAc/MeOH/H(2)O (1:10:1:10, v/v) at a flow rate of 1.5 mL/min. When the flow rate was increased from 1.0 to 3.0 mL/min, the retention of stationary phase decreased from 60.3% to 39.7% resulting in loss of peak resolution, while the stationary phase retention is stable with an increase in sample size from 25 to 200 mg. From 100 mg of the crude sample HSCCC separation yielded 4.0 mg of kaempferol 3-O-galactoside, 6.0 mg of kaempferol 3-O-glucoside and 9.0 mg of fraction I containing a mixture of hyperoside and isoquercitrin. Then, from 18 mg of fraction I, 3.0 mg of hyperoside and 11.0 mg isoquercitrin were separated by preparative HPLC by successive sample injection at every 100 min interval. Chemical structures of all these compounds were confirmed by MS and NMR.
高速逆流色谱法(HSCCC)已成功用于从黑加仑叶乙酸乙酯提取物中制备分离黄酮类化合物。HSCCC分离采用正己烷/乙酸乙酯/甲醇/水(1:10:1:10,v/v)组成的两相溶剂系统,流速为1.5 mL/min。当流速从1.0 mL/min增加到3.0 mL/min时,固定相保留率从60.3%降至39.7%,导致峰分辨率下降,而随着样品量从25 mg增加到200 mg,固定相保留率保持稳定。从100 mg粗样品中,HSCCC分离得到4.0 mg山柰酚3 - O - 半乳糖苷、6.0 mg山柰酚3 - O - 葡萄糖苷和9.0 mg含有金丝桃苷和异槲皮苷混合物的组分I。然后,从18 mg组分I中,通过制备型高效液相色谱法,每隔100 min连续进样,分离得到3.0 mg金丝桃苷和11.0 mg异槲皮苷。所有这些化合物的化学结构均通过质谱和核磁共振得以确证。