Scavone J M, Blyden G T, Greenblatt D J
Division of Clinical Pharmacology, Tufts University School of Medicine, Boston, Massachusetts.
Clin Pharmacokinet. 1989 Mar;16(3):180-5. doi: 10.2165/00003088-198916030-00004.
31 healthy male (n = 17) and female (n = 14) volunteers, aged 20 to 45 years, were divided into 4 groups and received on 3 separate occasions either: paracetamol (acetaminophen) 650mg intravenously (n = 9); alprazolam 1mg orally (n = 7); antipyrine (phenazone) 1g intravenously (n = 8); or lorazepam 2mg intravenously (n = 7). Doses were administered prior to influenza vaccine (0.5ml, intramuscularly) and at 7 and 21 days post-vaccination. The overall differences among the 3 trials in clearance of antipyrine were of borderline significance (p less than 0.0611), with a trend towards reduced clearance in both of the post-vaccination trials. There were no overall differences observed in the elimination half-life of antipyrine, nor were there significant differences between trials in cumulative urinary excretion or fractional recovery of intact antipyrine, 4-hydroxyantipyrine, norantipyrine, or 3-hydroxymethyl antipyrine. For paracetamol and alprazolam, there were no significant differences among the 3 trials in any of the kinetic variables. The elimination half-life of lorazepam varied significantly among trials, but differences were small and not systematic. Lorazepam clearance did not vary significantly among trials. Thus, clearance of drugs which undergo hepatic conjugative reactions such as glucuronidation and sulphation are unlikely to be affected by the coadministration of influenza vaccine. Furthermore, not all drugs which are biotransformed by hepatic microsomal oxidation necessarily have impaired clearance due to coadministration of influenza vaccine.
31名年龄在20至45岁之间的健康男性(n = 17)和女性(n = 14)志愿者被分为4组,在3个不同的场合分别接受以下治疗:静脉注射对乙酰氨基酚650mg(n = 9);口服阿普唑仑1mg(n = 7);静脉注射安替比林(非那宗)1g(n = 8);或静脉注射劳拉西泮2mg(n = 7)。在接种流感疫苗(0.5ml,肌肉注射)之前以及接种疫苗后7天和21天给药。安替比林清除率在3次试验中的总体差异具有临界显著性(p小于0.0611),在两次接种疫苗后的试验中均有清除率降低的趋势。安替比林的消除半衰期没有观察到总体差异,在累积尿排泄或完整安替比林、4-羟基安替比林、去甲安替比林或3-羟甲基安替比林的分数回收率方面,试验之间也没有显著差异。对于对乙酰氨基酚和阿普唑仑,在3次试验中的任何动力学变量上都没有显著差异。劳拉西泮的消除半衰期在试验之间有显著差异,但差异很小且无系统性。试验之间劳拉西泮清除率没有显著变化。因此,经历肝结合反应如葡萄糖醛酸化和硫酸化的药物的清除率不太可能受到流感疫苗联合给药的影响。此外,并非所有通过肝微粒体氧化进行生物转化的药物都会因流感疫苗联合给药而清除受损。