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Start Over Journal european journal of drug metabolism and pharmacokinetics Publisher springer-verlag
1,495 results

7. Clinical pharmacokinetics of ketoprofen enantiomers in wild type of Cyp 2c8 and Cyp 2c9 patients with rheumatoid arthritis

Author

Wojciech Romanowski, Franciszek K. Główka, Edmund Grześkowiak, Marta Karaźniewicz-Łada, and Dominika Rogozinska

Subjects
Ketoprofen, Adult, Male, Stereoselective pharmacokinetics, Bioavailability, Capillary zone electrophoresis, Cmax, Cytochrome P450, Urine, Pharmacology, Arthritis, Rheumatoid, Cytochrome P-450 CYP2C8, Pharmacokinetics, medicine, Synovial fluid, Humans, Pharmacology (medical), CYP2C8, CYP2C9, Aged, Cytochrome P-450 CYP2C9, Original Paper, Chemistry, Anti-Inflammatory Agents, Non-Steroidal, Stereoisomerism, Middle Aged, Pharmacogenetics, Female, Aryl Hydrocarbon Hydroxylases, medicine.drug
Abstract

Pharmacokinetics of ketoprofen (KTP) enantiomers has been studied in patients with rheumatoid arthritis (RA) following administration of a single oral dose of 100 mg rac-KTP during multidrug therapy taking into consideration the genotype of RA patients Concentrations of (-)-R and (+)-S enantiomers of KTP in plasma, urine and synovial fluid samples were determined using a validated HPCE method. The genotype of the patients was analyzed using PCR-RFLP method to determine the polymorphic variants of genes coding CYP2C8 and CYP2C9 isoenzymes. The levels of KTP enantiomers in synovial fluid at 4 h following administration were insignificantly greater [(-)-R = 1.34 ± 0.91 mg/L; (+)-S = 1.38 ± 0.91 mg/L] than in plasma [(-)-R = 1.15 ± 0.95 mg/L; (+)-S = 1.22 ± 0.95 mg/L]. The values of AUC(0-∞) were 11.89 ± 5.00 and 10.92 ± 4.10 mg h/L for (-)-R and (+)-S enantiomer, respectively, and were lower compared with data obtained in healthy volunteers following administration of the same dose of rac-KTP. But, no statistically significant differences were observed also for C (max), Cl, V (d), t (0.5) and MRT of KTP enantiomers. The total percentage of unchanged KTP eliminated with urine of RA patients was in the range of 30-50% of the administered dose. Though RA patients represented the same wild genotype, quite significant variabilities (Cl((-)-R ) = 2.37-13.50 L/h and Cl((+)-S ) = 2.44-9.90 L/h) existed in the pharmacokinetics parameters of KTP. We concluded that KTP data obtained from healthy volunteers cannot be sufficient to predict disposition of KTP enantiomers in RA patients, especially when undergoing long-term multidrug therapy.

Published
2011