Stereoselective Pharmacokinetics and Inversion of (R)‐ Ketoprofen in Healthy Volunteers
- 1 February 1998
- journal article
- Published by Wiley in The Journal of Clinical Pharmacology
- Vol. 38 (2S) , 3S-10S
- https://doi.org/10.1002/j.1552-4604.1998.tb04411.x
Abstract
The pharmacokinetics of ketoprofen enantiomers were evaluated after 25‐, 50‐, and 100‐mg doses of (R)‐ ketoprofen and 100 mg of racemic ketoprofen in 25 healthy volunteers (12 male and 13 female). The fractional inversion (Finv) of (R)‐ ketoprofen was 8.9 ± 3.3% using plasma data and 10.0 ± 2.2% using urine data. There were small (max) values was noted for both enantiomers. A total of 69% of the dose was recovered in the urine as (R)‐ and (S)‐ ketoprofen and conjugates. The elimination rate constant of (R)‐ ketoprofen was significantly different (P < 0.05) between men and women. Exposure to cyclooxygenase inhibiting (S)‐ ketoprofen was approximately 10% of the dose after the administration of pure (R)‐ ketoprofen and was independent of gender. J Clin Pharmacol 1998;38:3S‐10S.Keywords
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