High-performance Liquid Chromatographic Determination of Stereoselective Disposition of Carprofen in Humans
Authors:
- 1 November 1981
- journal article
- research article
- Published by Elsevier in Journal of Pharmaceutical Sciences
- Vol. 70 (11) , 1207-1212
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Metabolism of carprofen, a nonsteroidal anti-inflammatory agent, in rats, dogs, and humansJournal of Pharmaceutical Sciences, 1980
- Stereospecific Assay and Stereospecific Disposition of Racemic Carprofen in RatsJournal of Pharmaceutical Sciences, 1979
- Determination of the anti-inflammatory agent carprofen, (d,l)-6-chloro-α-methylcarbazole-2-actic acid, in blood by high-pressure liquid chromatographyJournal of Chromatography A, 1977
- Metabolism of the (+)-, (±)-, and (-)-Enantiomers of α-Methylfluorene-2-acetic Acid (Cicloprofen) in RatsXenobiotica, 1977
- Isomeric inversion of ibuprofen (r)‐enantiomer in humansJournal of Pharmaceutical Sciences, 1976
- Stereospecific Inversion ofl-α-Methylfluorene-2-acetic Acid to itsd-Enantiomer in the DogXenobiotica, 1976
- GLC Determination of Ibuprofen [dl-2-(p-Isobutylphenyl)propionic Acid] Enantiomers in Biological SpecimensJournal of Pharmaceutical Sciences, 1975
- Stereoisomeric relationships among anti-inflammatory activity, inhibition of platelet aggregation, and inhibition of prostaglandin synthetaseProstaglandins, 1975