Impact of reversed phase column pairs in comprehensive two-dimensional liquid chromatography

被引:14
作者
Allen, Robert C. [1 ]
Barnes, Brian B. [1 ]
Ahmad, Imad A. Haidar [1 ]
Filgueira, Marcelo R. [1 ]
Carr, Peter W. [1 ]
机构
[1] Univ Minnesota, Dept Chem, Minneapolis, MN 55455 USA
基金
美国国家科学基金会;
关键词
Comprehensive two dimensional liquid chromatography (LC x LC); Method development; Reverse phase; Column selection; Carbon-clad phase; Hydrophobic subtraction model; HYDROPHOBIC-SUBTRACTION MODEL; EFFECTIVE PEAK-CAPACITY; RESOLVING POWER; SELECTIVITY; SEPARATIONS; OPTIMIZATION; ORTHOGONALITY; DIMENSIONALITY; DEPENDENCE; SAMPLES;
D O I
10.1016/j.chroma.2014.08.012
中图分类号
Q5 [生物化学];
学科分类号
070307 [化学生物学];
摘要
A major issue in optimizing the resolving power of two-dimensional chromatographic separations is the choice of the two phases so as to maximize the distribution of the analytes over the separation space. In this work, we studied the choice of appropriate reversed phases to use in on-line comprehensive two-dimensional liquid chromatography (LC x LC). A set of four chemically different conventional bonded reversed phases was used in the first dimension. The second dimension column was either a conventional bonded C18 phase or a carbon-clad phase (CCP). The LC x LC chromatograms and contour plots were all rather similar indicating that the selectivities of the two phases were also similar regardless of the reverse phase column used in the first dimension. Further, the spatial coverage seen with all four first dimension stationary phases when paired with a second dimension C18 phase were low and the retention times were strongly correlated. However, when the C18 column was replaced with the CCP column much improved separations were observed with higher spatial coverages, greater orthogonalities and significant increases in the number of observed peaks. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:169 / 177
页数:9
相关论文
共 35 条
[1]
Improved Synthesis of Carbon-Clad Silica Stationary Phases [J].
Ahmad, Imad A. Haidar ;
Carr, Peter W. .
ANALYTICAL CHEMISTRY, 2013, 85 (24) :11765-11770
[2]
Boswell P.G., 2014, COLUMN SELECTIVITY D
[3]
Optimization of two-dimensional gradient liquid chromatography separations [J].
Cesla, Petr ;
Hajek, Tomas ;
Jandera, Pavel .
JOURNAL OF CHROMATOGRAPHY A, 2009, 1216 (16) :3443-3457
[4]
On-line comprehensive two-dimensional separations of charged compounds using reversed-phase high performance liquid chromatography and hydrophilic interaction chromatography. Part I: Orthogonality and practical peak capacity considerations [J].
D'Attoma, Amelie ;
Grivel, Candice ;
Heinisch, Sabine .
JOURNAL OF CHROMATOGRAPHY A, 2012, 1262 :148-159
[5]
Matched filtering with background suppression for improved quality of base peak chromatograms and mass spectra in liquid chromatography-mass spectrometry [J].
Danielsson, R ;
Bylund, D ;
Markides, KE .
ANALYTICA CHIMICA ACTA, 2002, 454 (02) :167-184
[6]
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
[7]
Selecting an "orthogonal" column during high-performance liquid chromatographic method development for samples that may contain non-ionized solutes [J].
Dolan, J. W. ;
Snyder, L. R. .
JOURNAL OF CHROMATOGRAPHY A, 2009, 1216 (16) :3467-3472
[8]
Dolan J.W., 2012, ADV CHROMATOGR, P297
[9]
Improving Peak Capacity in Fast Online Comprehensive Two-Dimensional Liquid Chromatography with Post-First-Dimension Flow Splitting [J].
Filgueira, Marcelo R. ;
Huang, Yuan ;
Witt, Klaus ;
Castells, Cecilia ;
Carr, Peter W. .
ANALYTICAL CHEMISTRY, 2011, 83 (24) :9531-9539
[10]
Giddings J.C., 1984, ANAL CHEM, V56, p1259A