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Lack of effect of gender and oral contraceptive steroids on the pharmacokinetics of (R)-ibuprofen in human.

机译:性别和口服避孕药类固醇对人体内(R) - 布洛芬药代动力学的影响不足。

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摘要

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.
机译:在健康成年男性,女性和女性使用口服避孕类固醇(OCS)组中研究了性别和口服避孕类固醇对(R)-布洛芬药代动力学的影响。两组之间的AUC,CLpo,t1 / 2和Vss,app值无显着差异。类似地,来自三组的合并血浆中(R)-布洛芬的未结合百分比在统计学上没有差异。由于手性倒置是人类中(R)-布洛芬清除率的主要决定因素,因此可以从这些数据推断出性别和OCS对(R)-布洛芬向药理活性S-对映体的转化影响很小或没有影响。此外,激素因素不太可能影响人肝长链脂肪酸:CoA连接酶的活性,该酶介导(R)-布洛芬倒置的速率限制步骤。

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