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Effects of caffeine on the kinetics of fluvoxamine and its major metabolite in plasma after a single oral dose of the drug.

机译:单次口服药物后,咖啡因对血浆中氟伏沙明及其主要代谢物动力学的影响。

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The effects of caffeine on the kinetics of fluvoxamine (FLV) and its major metabolite fluvoxamino acid (FLA) in plasma, after a single oral dose of the drug, were studied in 12 healthy male volunteers. The subjects received caffeine 300 mg/d or placebo for 11 days in a double-blind randomized crossover manner, and on the eighth day they received a single oral 50-mg dose of FLV. Blood sampling and pharmacodynamic evaluation were conducted up to 72 hours after FLV dosing. Plasma concentrations of FLV and FLA were measured by high-performance liquid chromatography. Caffeine significantly decreased the plasma concentrations at 6 time points (P<0.05) and total area under the plasma concentration-time curve (156.5+/-51.7 vs. 118.9+/-38.2 ng/h/mL, P<0.01) of FLV. Plasma concentration and pharmacokinetic parameters of FLA were not affected by caffeine. Caffeine induced no significant change in the pharmacodynamic effects of FLV. The present study suggests that caffeine slightly induces the metabolism of FLV, probably mediated by CYP1A2.
机译:在单次口服药物后,在12位健康的男性志愿者中研究了咖啡因对血浆中氟伏沙明(FLV)及其主要代谢物氟伏沙氨基酸(FLA)动力学的影响。受试者以双盲随机交叉方式接受咖啡因300 mg / d或安慰剂治疗11天,并在第八天接受口服单剂量50 mg FLV。 FLV给药后长达72小时进行了血液采样和药效学评估。通过高效液相色谱法测量FLV和FLA的血浆浓度。咖啡因显着降低了FLV的6个时间点的血浆浓度(P <0.05)和血浆浓度-时间曲线下的总面积(156.5 +/- 51.7对118.9 +/- 38.2 ng / h / mL,P <0.01) 。咖啡因不会影响FLA的血浆浓度和药代动力学参数。咖啡因对FLV的药效没有明显影响。本研究提示咖啡因可轻微诱导FLV的代谢,可能是由CYP1A2介导的。

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