Effect of first dimension phase selectivity in online comprehensive two dimensional liquid chromatography (LC x LC)

被引:19
作者
Gu, Haiwei [1 ]
Huang, Yuan [1 ]
Filgueira, Marcelo [1 ,2 ]
Carr, Peter W. [1 ]
机构
[1] Univ Minnesota, Dept Chem, Minneapolis, MN 55455 USA
[2] Univ Nacl La Plata, Div Quim Analit, Fac Ciencias Exactas, RA-1900 La Plata, Argentina
基金
美国国家科学基金会;
关键词
Two dimensional liquid chromatography; Selectivity; Reversed phase; LC x LC method development; Hydrophobic subtraction method; Carbon stationary phases; EFFECTIVE PEAK-CAPACITY; CARBON-COATED ZIRCONIA; SAMPLING TIME; PERFORMANCE; SEPARATION; COLUMN; OPTIMIZATION; RETENTION; DIMENSIONALITY; 2ND-DIMENSION;
D O I
10.1016/j.chroma.2011.07.063
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In this study, we examined the effect of first dimension column selectivity in reversed phase (RP) online comprehensive two dimensional liquid chromatography (LC x LC). The second dimension was always a carbon clad metal oxide reversed phase material. The hydrophobic subtraction model (HSM) and the related phase selective triangles were used to guide the selection of six different RP first dimension columns. Various kinds of samples were investigated and thus two different elution conditions were needed to cause full elution from the first dimension columns. We compared LC x LC chromatograms, contours plots, and f(coverage) plots by measuring peak capacities, peak numbers, relative spatial coverage, correlation values, etc. The major finding of this study is that the carbon phase due to its rather different selectivity from other reversed phases is reasonably orthogonal to a variety of common types of bonded reversed phases. Thus quite surprisingly the six different first dimension stationary phases all showed generally similar separation patterns when paired to the second dimension carbon phase. This result greatly simplifies the task of choosing the correct pair of phases for RP x RP. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:6675 / 6687
页数:13
相关论文
共 60 条
[1]   Comprehensive two-dimensional liquid chromatography separations of pharmaceutical samples using dual Fused-Core columns in the 2nd dimension [J].
Alexander, Anthony J. ;
Ma, Lianjia .
JOURNAL OF CHROMATOGRAPHY A, 2009, 1216 (09) :1338-1345
[2]   Optimal gradient operation in comprehensive liquid chromatography x liquid chromatography systems with limited orthogonality [J].
Bedani, Filippo ;
Kok, Wim Th. ;
Janssen, Hans-Gerd .
ANALYTICA CHIMICA ACTA, 2009, 654 (01) :77-84
[3]   AUTOMATED INSTRUMENTATION FOR COMPREHENSIVE 2-DIMENSIONAL HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY OF PROTEINS [J].
BUSHEY, MM ;
JORGENSON, JW .
ANALYTICAL CHEMISTRY, 1990, 62 (02) :161-167
[4]   Perspectives on Recent Advances in the Speed of High-Performance Liquid Chromatography [J].
Carr, Peter W. ;
Stoll, Dwight R. ;
Wang, Xiaoli .
ANALYTICAL CHEMISTRY, 2011, 83 (06) :1890-1900
[5]   Optimization of two-dimensional gradient liquid chromatography separations [J].
Cesla, Petr ;
Hajek, Tomas ;
Jandera, Pavel .
JOURNAL OF CHROMATOGRAPHY A, 2009, 1216 (16) :3443-3457
[6]  
Davis J. M., 2009, 238 ACS M WASH DC
[7]   Dependence of Effective Peak Capacity in Comprehensive Two-Dimensional Separations on the Distribution of Peak Capacity between the Two Dimensions [J].
Davis, Joe M. ;
Stoll, Dwight R. ;
Carr, Peter W. .
ANALYTICAL CHEMISTRY, 2008, 80 (21) :8122-8134
[8]   Effect of first-dimension undersampling on effective peak capacity in comprehensive two-dimensional separations [J].
Davis, Joe M. ;
Stoll, Dwight R. ;
Carr, Peter W. .
ANALYTICAL CHEMISTRY, 2008, 80 (02) :461-473
[9]   Metabolomics: Current analytical platforms and methodologies [J].
Dunn, WB ;
Ellis, DI .
TRAC-TRENDS IN ANALYTICAL CHEMISTRY, 2005, 24 (04) :285-294
[10]   2-DIMENSIONAL COLUMN LIQUID-CHROMATOGRAPHIC TECHNIQUE FOR RESOLUTION OF COMPLEX-MIXTURES [J].
ERNI, F ;
FREI, RW .
JOURNAL OF CHROMATOGRAPHY, 1978, 149 (FEB) :561-569