Comparative performances of selected chiral HPLC, SFC, and CE systems with a chemically diverse sample set

被引:38
作者
Borman, P
Boughtflower, B
Cattanach, K
Crane, K
Freebairn, K
Jonas, G
Mutton, I
Patel, A
Sanders, M
Thompson, D
机构
[1] GlaxoSmithKline, CASS, Discovery Res, Stevenage SG1 2NY, Herts, England
[2] GlaxoSmithKline, CASS, Harlow, Essex, England
[3] GlaxoSmithKline, Strateg Technol, Dartford, Kent, England
[4] GlaxoSmithKline, Chem Dev, Tonbridge, Kent, England
[5] GlaxoSmithKline, Strateg Technol, Stevenage, Herts, England
关键词
comparison; chiral phases; chiral selectors; HPLC; SFC; CE;
D O I
10.1002/chir.10260
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Pharmaceutical companies have a continuous need to resolve new racemates. Analysis may be required in aqueous and nonaqueous media, or in the presence of several different sets of potentially interfering compounds. There is often a preparative requirement. For these reasons analysts may require a number of different separation systems capable of resolving a given pair of enantiomers. We wished to improve upon existing approaches that address this situation and undertook a program of work to screen over 100 racemates, selected for their chemical diversity, on over 100 different chiral HPLC, SFC, and CE systems. Here we report results of this comparison and illustrate the use of rapid gradient screening as a valuable tool for chiral method development. (C) 2003 Wiley-Liss, Inc.
引用
收藏
页码:S1 / S12
页数:12
相关论文
共 42 条
[11]   Comparison and modeling study of vancomycin, ristocetin A, and teicoplanin for CE enantioseparations [J].
Gasper, MP ;
Berthod, A ;
Nair, UB ;
Armstrong, DW .
ANALYTICAL CHEMISTRY, 1996, 68 (15) :2501-2514
[12]   Chiral separation by chromatographic and electromigration techniques.: A review [J].
Gübitz, G ;
Schmid, MG .
BIOPHARMACEUTICS & DRUG DISPOSITION, 2001, 22 (7-8) :291-336
[13]   CELLULOSIC CHIRAL STATIONARY PHASE UNDER REVERSED-PHASE CONDITION [J].
ISHIKAWA, A ;
SHIBATA, T .
JOURNAL OF LIQUID CHROMATOGRAPHY, 1993, 16 (04) :859-878
[14]   Comparison of the enantioseparation of racemic uridine analogs on Whelk-O 1 and ChiralPak-AD columns [J].
Magora, A ;
Abu-Lafi, S ;
Levin, S .
JOURNAL OF CHROMATOGRAPHY A, 2000, 866 (02) :183-194
[15]   DIPHENYLETHANEDIAMINE (DPEDA) DERIVATIVES AS CHIRAL SELECTORS .4. A COMPARISON OF 3,5-DINITROBENZOYLATED (S,S)-DPEDA-DERIVED AND (S,R)-DPEDA-DERIVED CHIRAL STATIONARY PHASES WITH PIRKLES STANDARD (R)-PHENYLGLYCINE-DERIVED PHASE IN NORMAL-PHASE HPLC [J].
MAIER, NM ;
URAY, G ;
KLEIDERNIGG, OP ;
LINDNER, W .
CHIRALITY, 1994, 6 (02) :116-128
[16]   Knowledge-based system for method development of chiral separations with capillary electrophoresis using highly-sulphated cyclodextrins [J].
Matthijs, N ;
Perrin, C ;
Maftouh, M ;
Massart, DL ;
Vander Heyden, Y .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2002, 27 (3-4) :515-529
[17]   Chiral packed column subcritical fluid chromatography on polysaccharide and macrocyclic antibiotic chiral stationary phases. [J].
Medvedovici, A ;
Sandra, P ;
Toribio, L ;
David, F .
JOURNAL OF CHROMATOGRAPHY A, 1997, 785 (1-2) :159-171
[18]  
Morin P, 1999, ELECTROPHORESIS, V20, P2630, DOI 10.1002/(SICI)1522-2683(19990901)20:13<2630::AID-ELPS2630>3.0.CO
[19]  
2-9
[20]   RESOLUTION BY HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY USING POLYSACCHARIDE CARBAMATES AND BENZOATES AS CHIRAL STATIONARY PHASES [J].
OKAMOTO, Y ;
KAIDA, Y .
JOURNAL OF CHROMATOGRAPHY A, 1994, 666 (1-2) :403-419