Enantiomeric resolution of 2‐arylpropionic acid nonsteroidal anti‐inflammatory drugs by capillary electrophoresis: Methods and applications
- 17 August 2004
- journal article
- review article
- Published by Wiley in Electrophoresis
- Vol. 25 (16) , 2625-2656
- https://doi.org/10.1002/elps.200405928
Abstract
The 2‐arylpropionic acids (2‐APAs) are an important group of nonsteroidal anti‐inflammatory drugs. These agents, the majority of which are available as racemates, exhibit stereoselectivity in both their action and disposition. Developments in stereoselective separation science methodology, mainly chromatographic, have facilitated an evaluation of the pharmacological properties of the individual enantiomers of these drugs and contributed to our understanding of both their mode(s) of action and disposition. While a number of electrophoretic techniques, including capillary electrophoresis, capillary electrochromatography and isotachophoresis, have been applied to the stereoselective resolution and stereospecific analysis of these agents using a variety of chiral selectors, e.g., cyclodextrins, oligosaccharides, macrocyclic antibiotics, and proteins, the number of published applications in pharmaceutical and biomedical analysis remains relatively limited. However, the utility of electrophoretic techniques for stereospecific analysis may be illustrated using the 2‐APAs as typical examples of chiral acidic pharmaceuticals. Applications include: determination of enantiomeric composition following biosynthetic stereoselective hydrolysis; examination of both achiral and chiral impurity profiles in bulk drugs and formulated products; determination of enantiomeric impurities in both bulk drugs and formulated products; examination of configurational stability following stress testing of formulated products; determination of enantiomeric composition and metabolite profile in biological fluids following administration of the racemates and individual enantiomers. It may be anticipated that future exploitation of electrophoretic approaches to the stereospecific analysis of these agents will result in further contributions to our understanding of their stereoselective biological properties and therapeutic use.Keywords
This publication has 100 references indexed in Scilit:
- Treatment and survival study in the C57BL/6J-APCMin/+ (Min) mouse with R-flurbiprofenLife Sciences, 2000
- Avoparcin, a new macrocyclic antibiotic chiral run buffer additive for capillary electrophoresisElectrophoresis, 1999
- Clinical Endoscopic Evaluation of the Gastroduodenal Tolerance to (R)‐ Ketoprofen, (R)‐ Flurbiprofen, Racemic Ketoprofen, and Paracetamol: A Randomized, Single‐Blind, Placebo‐Controlled TrialThe Journal of Clinical Pharmacology, 1998
- Synthesis, absolute configuration and pharmacological evaluation of tiaprofenic acid antipodesEuropean Journal of Medicinal Chemistry, 1997
- Antiproliferative Effects of the Enantiomers of FlurbiprofenThe Journal of Clinical Pharmacology, 1996
- Stereoselective Inhibition of Inducible Cyclooxygenase by Chiral Nonsteroidal Antiinflammatory DrugsThe Journal of Clinical Pharmacology, 1996
- Capillary electrophoretic enantiomeric separations using the glycopeptide antibiotic, teicoplaninChirality, 1996
- Pure Enantiomers of 2‐Arylpropionic Acids: Tools in Pain Research and Improved Drugs in RheumatologyThe Journal of Clinical Pharmacology, 1992
- Aspirin-like drugs may block pain independently of prostaglandin synthesis inhibitionCellular and Molecular Life Sciences, 1991
- Enantiomers in arthritic disordersPharmacology & Therapeutics, 1990