Ochs H R, Greenblatt D J, Burstein E S
Br J Clin Pharmacol. 1987 Jun;23(6):759-63. doi: 10.1111/j.1365-2125.1987.tb03112.x.
The influence of cigarette smoking on the pharmacokinetics of a single dose of the triazolobenzodiazepine hypnotic triazolam was evaluated in 12 healthy nonsmoking male volunteers and in 12 male subjects, matched for age, height and weight, who smoked an average of 24 cigarettes a day (range: 15-30). Triazolam kinetics were determined from multiple serum concentrations measured during 15 h after a single 0.5 mg dose. There were no significant differences between nonsmoking controls and cigarette smokers in the peak serum triazolam concentration (4.64 vs 4.73 ng ml-1), the time of peak concentration (0.98 vs 1.0 h after dosage), elimination half-life (2.8 vs 2.5 h), or oral clearance of triazolam (506 vs 627 ml min-1). Likewise there were no significant differences between groups in the extent of triazolam binding to serum protein (18.8 vs 18.5% unbound). Altered pharmacodynamics of triazolam in cigarette smokers are not likely to be explained by altered pharmacokinetics.
在12名健康的不吸烟男性志愿者以及12名年龄、身高和体重匹配且平均每天吸烟24支(范围:15 - 30支)的男性受试者中,评估了吸烟对单剂量三唑并苯二氮䓬类催眠药三唑仑药代动力学的影响。单次服用0.5 mg剂量后,在15小时内通过多次测量血清浓度来确定三唑仑的动力学。在血清三唑仑峰值浓度(4.64对4.73 ng/ml)、峰值浓度出现时间(给药后0.98对1.0小时)、消除半衰期(2.8对2.5小时)或三唑仑的口服清除率(506对627 ml/min)方面,不吸烟对照组和吸烟者之间没有显著差异。同样,两组之间三唑仑与血清蛋白结合程度(未结合率18.8%对18.5%)也没有显著差异。吸烟者中三唑仑药效学的改变不太可能用其药代动力学的改变来解释。