Evaluation of generic chiral liquid chromatography screens for pharmaceutical analysis

被引:94
作者
Anderson, ME [1 ]
Aslan, D
Clarke, A
Roeraade, J
Hagman, G
机构
[1] AstraZeneca, Proc R&D, Dept Analyt Chem, SE-15185 Sodertalje, Sweden
[2] AstraZeneca, Proc R&D, Dept Analyt Chem, Loughborough LE11 5RH, Leics, England
[3] Royal Inst Technol, Dept Analyt Chem, SE-10044 Stockholm, Sweden
关键词
pharmaceutical analysis; chiral stationary phases; LC; enantiomer separation;
D O I
10.1016/S0021-9673(03)00888-4
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Two different automated generic liquid chromatography screens for the separation of chiral compounds of pharmaceutical interest have been evaluated. The test set comprised 53 chemically diverse chiral compounds involving 55 enantiomeric pairs from the pharmaceutical industry (i.e. starting materials, synthetic intermediates and drug substances). The first screen utilised four polysaccharide-based columns with five mobile phases and showed enantioselectivity for 87% of the test compounds. The second screen employed three macrocyclic glycopeptide columns with two mobile phases and showed enantioselectivity for 65% of the test compounds. Merging of the two screening procedures resulted in an enantioselectivity for 96% of the chiral compounds. It is anticipated that the systematic use of the automated chiral HPLC screens described in this report will substantially reduce the necessary time for method development of pharmaceutically related chiral analytical methods. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:83 / 101
页数:19
相关论文
共 30 条
[1]   Optimization strategies for HPLC enantio separation of racemic drugs using polysaccharides and macrocyclic glycopeptide antibiotic chiral stationary phases [J].
Aboul-Enein, HY ;
Ali, M .
FARMACO, 2002, 57 (07) :513-529
[2]  
*AST, 2002, CHIR HDB
[3]  
Beesley T. E., 1998, SEPAR SCI S
[4]   Separation of chiral sulfoxides by liquid chromatography using macrocyclic glycopeptide chiral stationary phases [J].
Berthod, A ;
Xiao, TL ;
Liu, Y ;
Jenks, WS ;
Armstrong, DW .
JOURNAL OF CHROMATOGRAPHY A, 2002, 955 (01) :53-69
[5]  
Branch S.K., 2001, CHIRAL SEPARATION TE, P317
[6]   Enantioseparation of selected chiral sulfoxides using polysaccharide-type chiral stationary phases and polar organic, polar aqueous-organic and normal-phase eluents [J].
Chankvetadze, B ;
Yamamoto, C ;
Okamoto, Y .
JOURNAL OF CHROMATOGRAPHY A, 2001, 922 (1-2) :127-137
[7]   Comparative enantioseparation of selected chiral drugs on four different polysaccharide-type chiral stationary phases using polar organic mobile phases [J].
Chankvetadze, B ;
Kartozia, I ;
Yamamoto, C ;
Okamoto, Y .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2002, 27 (3-4) :467-478
[8]  
Chankvetadze B., 1997, CAPILLARY ELECTROPHO, P1
[9]  
Chapman J, 2001, LC GC N AM, V19, P427
[10]   Impact of normal-phase gradient elution in chiral chromatography: a novel, robust, efficient and rapid chiral screening procedure [J].
de la Puente, ML ;
White, CT ;
Rivera-Sagredo, A ;
Reilly, J ;
Burton, K ;
Harvey, G .
JOURNAL OF CHROMATOGRAPHY A, 2003, 983 (1-2) :101-114