Sensitive high-performance liquid chromatographic method for direct separation of labetalol stereoisomers in biological fluids using an α1-acid glycoprotein stationary phase

This publication has 12 references indexed in Scilit:

• Reversed-phase high-performance liquid chromatographic separation of the stereoisomers of labetalol via derivatization with chiral and non-chiral isothiocyanate reagents
  Journal of Chromatography B: Biomedical Sciences and Applications, 1992
• Sensitive microbore high-performance liquid chromatographic assay for labetatol in the fluids of pregnant sheep
  Journal of Chromatography B: Biomedical Sciences and Applications, 1991
• Labetalol pharmacokinetics and pharmacodynamics: Evidence of stereoselective disposition
  Clinical Pharmacology & Therapeutics, 1990
• Chiral separations of cationic and anionic drugs on an α1-acid glycoprotein-bonded stationary phase (enantiopac®) : II. Influence of mobile phase additives and pH on chiral resolution and retention
  Journal of Chromatography A, 1986
• Chiral Separation of Cationic Drugs on an α₁-Acid Glycoprotein Bonded Stationary Phase
  Journal of Liquid Chromatography, 1986
• Resolution of racemic aminoalcohols (β-blockers), amines and acids as enantiomeric derivatives using a chiral α1-acid glycoprotein column
  Journal of Chromatography A, 1985
• Synthesis and comparison of some cardiovascular properties of the stereoisomers of labetalol
  Journal of Medicinal Chemistry, 1982
• THE α‐ AND β‐ADRENOCEPTOR BLOCKING POTENCIES OF LABETALOL AND ITS INDIVIDUAL STEREOISOMERS IN ANAESTHETIZED DOGS AND IN ISOLATED TISSUES
  British Journal of Pharmacology, 1982
• Arylethanolamines derived from salicylamide with .alpha.- and .beta.-adrenoceptor blocking activities. Preparation of labetalol, its enantiomers and related salicylamides
  Journal of Medicinal Chemistry, 1982
• Alpha- and Beta-Blocking Activities of Racemates of Labetalol
  The Japanese Journal of Pharmacology, 1980