Two-dimensional reversed-phase liquid chromatography using two monolithic silica C18 columns and different mobile phase modifiers in the two dimensions

被引:84
作者
Ikegami, T [1 ]
Hara, T
Kimura, H
Kobayashi, H
Hosoya, K
Cabrera, K
Tanaka, N
机构
[1] Kyoto Inst Technol, Dept Polymer Sci & Engn, Sakyo Ku, Kyoto 6068585, Japan
[2] Merck KGaA, Res & Dev, D-64293 Darmstadt, Germany
关键词
2D-HPLC; monolithic silica columns; organic modifiers;
D O I
10.1016/j.chroma.2005.10.068
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Comprehensive two-dimensional (2D) HPLC in the reversed-phase liquid chromatography (RPLC) mode using C18 silica monolith columns at first dimension (1 st-D) (10 cm x 4.6 mm I.D.) and second dimension (2nd-D) (5 cm x 4.6 mm I.D.) was carried out successfully. A mixture of water and tetrahydrofuran (THF) was used as a mobile phase in the I st-D separation, and a mixture of water and methanol (CH3 OH) in the 2nd-D separation. Sample fractions from 1st-D column were directly loaded into an injection loop of the 2nd-D HPLC equipped with two injector valves for one column. The fractionation time at the 1st-D that was equal to the separation time at the 2nd-D was 45 or 60 s. Total peak capacity up to 900 was obtained in about 60 min for the isocratic mode separation of aromatic compounds in this system. Gradient elution mode applied to both 1st-D and 2nd-D separations resulted in shorter separation time and better separation efficiencies than the isocratic mode. It was demonstrated that 2D-HPLC systems employing popular C18 stationary phases with different organic modifiers in mobile phases for each dimension could produce large peak capacity. The different selectivities were provided by the difference in polar interactions between a solute and the organic modifier existing in the stationary phase. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:112 / 117
页数:6
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