O'Reilly R A, Trager W F, Motley C H, Howald W
Clin Pharmacol Ther. 1980 Aug;28(2):187-95. doi: 10.1038/clpt.1980.149.
To evaluate the interaction of secobarbital with racemic warfarin or R,S(+/-)-warfarin, S(-)-warfarin was synthesized with 13C-label in the 2-position of the coumarin nucleus and added to 12C-R(+)-warfarin to form a 12C-/13C-warfarin pseudoracemate. Six normal subjects received 1.5 mg/kg of this "cold-labeled" pseudoracemate. It was given with and without a daily oral dose of secobarbital, 100 mg, beginning 7 days before the warfarin and continuing throughout the hypoprothrombinemia. Plasma samples were obtained daily and analyzed for warfarin and for one-stage prothrombin activity. Unchanged warfarin in plasma was fractionated by forward-phase high-pressure liquid chromatography, and enantiomorphic ratios were determined by chemical ionization-mass spectrometry with pentadeuterio-warfarin as the internal standard. There was a reduction of the hypoprothrombinemia of the pseuoracemate during the secobarbital regimen over that on warfarin alone (p < 0.001). There was an increase in plasma clearance of R-warfarin (p < 0.05) and an increase in plasma clearance of S-warfarin (p < 0.003) during the secobarbital regimen over that on warfarin alone. It was concluded that secobarbital diminished the hypoprothrombinemia of pseudoracemic warfarin by increasing plasma clearance of the more hypoprothrombinemic S-warfarin and by increasing plasma clearance of the less hypoprothombinemic R-warfarin.
为评估速可巴比妥与消旋华法林或R,S(+/-)-华法林的相互作用,在香豆素核的2位用13C标记合成了S(-)-华法林,并将其添加到12C-R(+)-华法林中,形成12C-/13C-华法林假外消旋体。6名正常受试者接受了1.5mg/kg的这种“冷标记”假外消旋体。在服用华法林前7天开始,每日口服100mg速可巴比妥,持续至低凝血酶原血症期间,分别在有和没有速可巴比妥的情况下给予该假外消旋体。每天采集血浆样本,分析华法林和一期凝血酶原活性。血浆中未变化的华法林通过正相高压液相色谱进行分离,对映体比例以十五氘代华法林为内标通过化学电离质谱法测定。与单独使用华法林相比,速可巴比妥治疗期间假外消旋体的低凝血酶原血症有所减轻(p<0.001)。与单独使用华法林相比,速可巴比妥治疗期间R-华法林的血浆清除率增加(p<0.05),S-华法林的血浆清除率增加(p<0.003)。得出的结论是,速可巴比妥通过增加低凝血酶原血症更明显的S-华法林的血浆清除率以及增加低凝血酶原血症较轻的R-华法林的血浆清除率,减轻了假外消旋体华法林的低凝血酶原血症。