Enantioselective chromatography in drug discovery.

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.

[1]  D. Armstrong,et al.  Role of the carbohydrate moieties in chiral recognition on teicoplanin-based LC stationary phases. , 2000, Analytical chemistry.

[2]  W. Lindner,et al.  Separation of enantiomers: needs, challenges, perspectives. , 2001, Journal of chromatography. A.

[3]  S. Peper,et al.  Simulated moving bed chromatography with supercritical fluids for the resolution of bi-naphthol enantiomers and phytol isomers. , 2002, Journal of biochemical and biophysical methods.

[4]  K. Gahm,et al.  Enantioselective separation of racemic secondary amines on a chiral crown ether-based liquid chromatography stationary phase. , 2002, Journal of chromatography. A.

[5]  D. Armstrong,et al.  A new approach for the direct resolution of racemic beta adrenergic blocking agents by HPLC , 1992 .

[6]  G. Scriba Selected fundamental aspects of chiral electromigration techniques and their application to pharmaceutical and biomedical analysis. , 2002, Journal of pharmaceutical and biomedical analysis.

[7]  Liron Levy,et al.  Trends in the development of chiral drugs. , 2004, Drug discovery today.

[8]  D. Armstrong,et al.  Multiple enantioselective retention mechanisms on derivatized cyclodextrin gas chromatographic chiral stationary phases. , 1992 .

[9]  Koji Otsuka,et al.  Electrokinetic separations with micellar solutions and open-tubular capillaries , 1984 .

[10]  C. Wolf,et al.  Synthesis and evaluation of a copolymeric chiral stationary phase , 1998 .

[11]  Ernest L. Eliel,et al.  Stereochemistry of Organic Compounds , 1962 .

[12]  K. Hatada,et al.  Chromatographic resolution. 7. Useful chiral packing materials for high-performance liquid chromatographic resolution of enantiomers: phenylcarbamates of polysaccharides coated on silica gel , 1984 .

[13]  C M Grill,et al.  Closed-loop recycling with periodic intra-profile injection: a new binary preparative chromatographic technique. , 1998, Journal of chromatography. A.

[14]  Simulated moving columns technique for chiral liquid chromatography. , 2004, Journal of chromatography. A.

[15]  V. Schurig Separation of enantiomers by gas chromatography. , 2001, Journal of chromatography. A.

[16]  D. Armstrong,et al.  REVERSAL OF ENANTIOMERIC ELUTION ORDER ON MACROCYCLIC GLYCOPEPTIDE CHIRAL STATIONARY PHASES , 2001 .

[17]  R. Stringham,et al.  Effect of mobile phase acidic additives on enantioselectivity for phenylalanine analogs. , 2001, Journal of chromatography. A.

[18]  M. Okamoto Reversal of elution order during the chiral separation in high performance liquid chromatography. , 2002, Journal of pharmaceutical and biomedical analysis.

[19]  Shalini Andersson,et al.  Preparative chiral chromatographic resolution of enantiomers in drug discovery. , 2002, Journal of biochemical and biophysical methods.

[20]  D. Armstrong,et al.  High Efficiency Liquid and Super‐/Subcritical Fluid‐Based Enantiomeric Separations: An Overview , 2004 .

[21]  E. Francotte Chromatography as a Separation Tool for the Preparative Resolution of Racemic Compounds , 1997 .

[22]  Tao Wang,et al.  Effects of alcohol mobile-phase modifiers on the structure and chiral selectivity of amylose tris(3,5-dimethylphenylcarbamate) chiral stationary phase. , 2003, Journal of chromatography. A.

[23]  D. Armstrong,et al.  Facile liquid chromatographic enantioresolution of native amino acids and peptides using a teicoplanin chiral stationary phase. , 1996, Journal of chromatography. A.

[24]  O. Mcconnell,et al.  Rapid method development for chiral separation in drug discovery using multi-column parallel screening and circular dichroism signal pooling. , 2004, Journal of chromatography. A.

[25]  D. Armstrong,et al.  Fast Super/Subcritical Fluid Chromatography Enantiomeric Separations of Dihydrofurocoumarin Derivatives with Macrocyclic Glycopeptide Stationary Phases , 2003, Chromatographia.

[26]  T. L. Chester,et al.  Supercritical fluid and unified chromatography. , 2000, Analytical chemistry.

[27]  V. Schurig,et al.  Recent progress in enantiomer separation by capillary electrochromatography , 2000, Electrophoresis.

[28]  E. Francotte,et al.  Enantioselective chromatography as a powerful alternative for the preparation of drug enantiomers. , 2001, Journal of chromatography. A.

[29]  L. J. Brice,et al.  Liquid and subcritical CO2 separations of enantiomers on a broadly applicable polysiloxane chiral stationary phase , 1996 .

[30]  J. Caldwell Importance of stereospecific bioanalytical monitoring in drug development. , 1996, Journal of chromatography. A.

[31]  H. Aboul‐Enein,et al.  The Impact of Stereochemistry on Drug Development and Use , 1997 .

[32]  R. Stringham,et al.  Effect of amine mobile phase additives on chiral subcritical fluid chromatography using polysaccharide stationary phases. , 2004, Journal of chromatography. A.

[33]  R. Stringham,et al.  Memory effect of mobile phase additives in chiral separations on a Chiralpak AD column. , 2002, Journal of chromatography. A.

[34]  R. Rosset,et al.  Supercritical and subcritical fluid chromatography on a chiral stationary phase for the resolution of phosphine oxide enantiomers , 1985 .

[35]  K. Phinney SFC of drug enantiomers. , 2000, Analytical chemistry.

[36]  R. Stringham,et al.  Memory effect of diethylamine mobile phase additive on chiral separations on polysaccharide stationary phases. , 2004, Chirality.

[37]  BruceM. Cohen Automated Column and Solvent Selection for Fully Automated HPLC Analyses of Tablet Content Uniformity , 1987 .

[38]  G. Subramanian A practical approach to chiral separations by liquid chromatography , 1994 .

[39]  G. Terfloth Enantioseparations in super- and subcritical fluid chromatography. , 2001, Journal of chromatography. A.