Abstract
The importance of stereochemistry in the disposition of the 2-⌽-propionic acid NSAID’s* is outlined. General approaches for the Chromatographic resolution of these agents by both direct and indirect methods are briefly reviewed. Problems associated with the choice of HPLC mobile phase for the resolution of, and derivatization methods for the formation of, stable diastereoisomeric derivatives are illustrated with reference to pirprofen. The application of chiral mobile phases and commercially available HPLC CSP’s to the analysis of these agents is examined, and problems which may arise during the ‘work-up’ of samples of biological origin are discussed.
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Abbreviations
- NSAID:
-
non-steroidal antirinflammatory drug
- THF:
-
tetrahydrofuran
- DMOA:
-
N,N-dimethyloctylamine
- CSP:
-
chiral stationary phase
- RP:
-
reversed phase
- MS:
-
mass spectrometry (EI, electron impact)
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Hutt, A.J., Caldwell, J. (1988). Enantiomeric Analysis of 2-Phenylpropionic Acid NSAID’s in Biological Fluids by HPLC. In: Reid, E., Robinson, J.D., Wilson, I.D. (eds) Bioanalysis of Drugs and Metabolites, Especially Anti-Inflammatory and Cardiovascular. Methodological Surveys in Biochemistry and Analysis, vol 18 A. Springer, Boston, MA. https://doi.org/10.1007/978-1-4757-9424-3_14
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DOI: https://doi.org/10.1007/978-1-4757-9424-3_14
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