Orthogonal separations for reversed-phase liquid chromatography

被引:84
作者
Pellett, J
Lukulay, P
Mao, Y
Bowen, W
Reed, R
Ma, M
Munger, RC
Dolan, JW
Wrisley, L
Medwid, K
Toltl, NP
Chan, CC
Skibic, M
Biswas, K
Wells, KA
Snyder, LR
机构
[1] LC Resources, Orinda, CA 94563 USA
[2] Analyt R&D, Michigan Labs, Pfizer Global Res & Dev Pharmaceut Sci, Ann Arbor, MI USA
[3] Merck & Co Inc, Pharmaceut Res & Dev, Pharmaceut Anal & Control, West Point, PA 19486 USA
[4] Amgen Inc, Analyt Sci, Thousand Oaks, CA 91320 USA
[5] BASi NW Lab, McMinnville, OR 97128 USA
[6] Wyeth Res, Pearl River, NY 10965 USA
[7] Eli Lilly Canada, Toronto, ON, Canada
[8] Eli Lilly, Indianapolis, IN USA
关键词
reversed-phase liquid chromatography; orthogonal method; pharmaceutical analysis;
D O I
10.1016/j.chroma.2005.09.080
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A general procedure is proposed for the rapid development of a reversed-phase liquid chromatographic (RP-LC) separation that is "orthogonal" to a pre-existing ("primary") method for the RP-LC separation of a given sample. The procedure involves a change of the mobile-phase organic solvent (B-solvent), the replacement of the primary column by one of very different selectivity, and (only if necessary) a change in mobile phase pH or the use of a third column. Following the selection of the "orthogonal" B-solvent, column and mobile phase pH, further optimization of peak spacing and resolution can be achieved by varying separation temperature and either isocratic %B or gradient time. The relative "orthogonality" of the primary and "orthogonal" RP-LC methods is then evaluated from plots of retention for one method versus the other. The present procedure was used to develop "orthogonal" methods for nine routine RP-LC methods from six pharmaceutical analysis laboratories. The relative success of this approach can be judged from the results reported here. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:122 / 135
页数:14
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