Pieters F A, Woonink F, Zuidema J
Department of Biopharmaceutics, University of Amsterdam, The Netherlands.
Eur J Clin Pharmacol. 1988;34(1):73-6. doi: 10.1007/BF01061421.
In leprosy patients in Nigeria the influence of daily clofazimine and of once-monthly rifampicin on the pharmacokinetics of dapsone has been investigated. Three days after rifampicin the elimination half-life of dapsone was reduced from 40.4 to 25.3 h (n = 23). Correspondingly, the plasma dapsone 24 h after the last dose had fallen significantly from 2.63 to 2.02 mg/l. Clofazimine did not cause change in the pharmacokinetics of dapsone. It was concluded that, although rifampicin had a considerable influence on the pharmacokinetics of dapsone, there is no reason to adjust the dose of dapsone during multidrug therapy of leprosy.
在尼日利亚的麻风病患者中,研究了每日服用氯法齐明和每月服用一次利福平对氨苯砜药代动力学的影响。服用利福平三天后,氨苯砜的消除半衰期从40.4小时降至25.3小时(n = 23)。相应地,末次给药后24小时血浆氨苯砜浓度从2.63毫克/升显著降至2.02毫克/升。氯法齐明未引起氨苯砜药代动力学的改变。得出的结论是,尽管利福平对氨苯砜的药代动力学有相当大的影响,但在麻风病的多药治疗期间没有理由调整氨苯砜的剂量。