Enantioselective chromatography in drug discovery

被引:176
作者
Zhang, Y [1 ]
Wu, DR [1 ]
Wang-Iverson, DB [1 ]
Tymiak, AA [1 ]
机构
[1] Bristol Myers Squibb Co, Pharmaceut Res Inst, Discovery Analyt Sci, Princeton, NJ 08648 USA
关键词
D O I
10.1016/S1359-6446(05)03407-0
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Molecular chirality is a fundamental consideration in drug discovery, one necessary to understand and describe biological targets as well as to design effective pharmaceutical agents. Enantioselective chromatography has played an increasing role not only as an analytical tool for chiral analyses, but also as a preparative technique to obtain pure enantiomers from racemates quickly from a wide diversity of chemical structures. Different enantioselective chromatography techniques are reviewed here, with particular emphasis on the most widespread high performance liquid chromatography (HPLC) and the rapidly emerging supercritical fluid chromatography (SFC) techniques. This review focuses on the dramatic advances in the chiral stationary phases (CSPs) that have made HPLC and SFC indispensable techniques for drug discovery today. In addition, screening strategies for rapid method development and considerations for laboratory-scale preparative separation are discussed and recent achievements are highlighted.
引用
收藏
页码:571 / 577
页数:7
相关论文
共 55 条
[1]  
ABOULENEIN HY, 1997, CHEM ANAL SERIES, V142
[2]  
Ahuja S., 2000, CHIRAL SEPARATION CH
[3]  
Ahuja S., 1997, Chiral Separations Applications and technology, V1st
[4]   Preparative chiral chromatographic resolution of enantiomers in drug discovery [J].
Andersson, S ;
Allenmark, SG .
JOURNAL OF BIOCHEMICAL AND BIOPHYSICAL METHODS, 2002, 54 (1-3) :11-23
[5]   A NEW APPROACH FOR THE DIRECT RESOLUTION OF RACEMIC BETA-ADRENERGIC BLOCKING-AGENTS BY HPLC [J].
ARMSTRONG, DW ;
CHEN, S ;
CHANG, C ;
CHANG, S .
JOURNAL OF LIQUID CHROMATOGRAPHY, 1992, 15 (03) :545-556
[6]  
*ASTEC, 1999, CHIR HDB
[7]  
BEESLEY TE, 2003, RECENT DEV LC COLUMN
[8]   Role of the carbohydrate moieties in chiral recognition on teicoplanin-based LC stationary phases [J].
Berthod, A ;
Chen, XH ;
Kullman, JP ;
Armstrong, DW ;
Gasparrini, F ;
D'Acquarica, I ;
Villani, C ;
Carotti, A .
ANALYTICAL CHEMISTRY, 2000, 72 (08) :1767-1780
[9]   MULTIPLE ENANTIOSELECTIVE RETENTION MECHANISMS ON DERIVATIZED CYCLODEXTRIN GAS-CHROMATOGRAPHIC CHIRAL STATIONARY PHASES [J].
BERTHOD, A ;
LI, WY ;
ARMSTRONG, DW .
ANALYTICAL CHEMISTRY, 1992, 64 (08) :873-879
[10]   Facile liquid chromatographic enantioresolution of native amino acids and peptides using a teicoplanin chiral stationary phase [J].
Berthod, A ;
Liu, YB ;
Bagwill, C ;
Armstrong, DW .
JOURNAL OF CHROMATOGRAPHY A, 1996, 731 (1-2) :123-137