Purification of quinoline yellow components using high-speed counter-current chromatography by stepwise increasing the flow-rate of the mobile phase

被引:39
作者
Oka, H [1 ]
Harada, KI
Suzuki, M
Fujii, K
Iwaya, M
Ito, Y
Goto, T
Matsumoto, H
Ito, Y
机构
[1] Aichi Prefectural Inst Publ Hlth, Kita Ku, Nagoya, Aichi 4628576, Japan
[2] Meijo Univ, Fac Pharm, Nagoya, Aichi 4688503, Japan
[3] NHLBI, Biophys Chem Lab, NIH, Bethesda, MD 20892 USA
关键词
counter-current chromatography; flow-rate; quinotine yellow; dyes; sulfonates;
D O I
10.1016/S0021-9673(03)00118-3
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Quinoline yellow (Color Index No. 47005) consists of multiple components that show a large difference in their partition coefficients (K), ranging from 0.03 to 3.3 in the solvent system tert.-butyl methyl ether (MTBE)-1wbutanol-acetonitrile-aqueous 0.1 M trifluoroacetic acid (TFA). Consequently, it requires an excessively long elution time for the simultaneous separation of all components by the standard high-speed counter-current chromatography technique, which uses a constant flow-rate of the mobile phase. In order to overcome this problem, we increased the flow-rate of the mobile phase stepwise from 0.1 to 2.0 mL/min. Using this new procedure, six components (0.2-6.1 mg) were successfully isolated from 25 mg of a commercial quinoline yellow preparation in a single run using a two-phase solvent system composed of MTBE-1-butanol-acetonitrile-aqueous 0.1 M TFA (1:3:1:5, v/v). The purified components were analyzed by high-performance liquid chromatography, electrospray ionization mass spectrometry, and nuclear magnetic resonance spectroscopy. (C) 2003 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:249 / 255
页数:7
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