| Literature DB >> 8562298 |
K M Knights1, C F McLean, A L Tonkin, J O Miners.
Abstract
The effects of gender and oral contraceptive steroids on the pharmacokinetics of (R)-ibuprofen were studied in groups of healthy adult males, females and oral contraceptive steroid (OCS) using females. The values of AUC, CLpo, t1/2 and Vss, app did not differ significantly between the groups. Similarly, the percentage unbound of (R)-ibuprofen in pooled plasma from the three groups was not statistically different. Since chiral inversion is the major determinant of (R)-ibuprofen clearance in humans, it may be inferred from these data that gender and OCS have little or no effect on conversion of (R)-ibuprofen to the pharmacologically active S-enantiomer. Moreover, it is unlikely that hormonal factors influence the activity of the human hepatic long-chain fatty-acid:CoA ligase, the enzyme mediating the rate limiting step of (R)-ibuprofen inversion.Entities:
Keywords: Australia; Biology; Comparative Studies; Contraception; Contraceptive Methods--pharmacodynamics; Developed Countries; Drug Interactions; Drugs; Enzymes; Enzymes And Enzyme Inhibitors; Family Planning; Gender Issues; Oceania; Oral Contraceptives, Combined--pharmacodynamics; Oral Contraceptives--pharmacodynamics; Physiology; Research Methodology; Research Report; Studies; Treatment
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Year: 1995 PMID: 8562298 PMCID: PMC1365175 DOI: 10.1111/j.1365-2125.1995.tb05769.x
Source DB: PubMed Journal: Br J Clin Pharmacol ISSN: 0306-5251 Impact factor: 4.335