Self T H, Self M M, Worden J P, Taylor W S, Straughn A B
Res Commun Chem Pathol Pharmacol. 1982 Dec;38(3):505-8.
The pharmacokinetic disposition of theophylline after a single 10mg/kg intravenous dose of aminophylline was evaluated in six rabbits. Three then received rifampin (50mg/kg) a day for 14 days and the disposition of theophylline was re-evaluated in all six rabbits after another 10mg/kg aminophylline dose. The mean theophylline half life before rifampin treatment of 5.11 +/- 0.71 hrs was not different (p greater than 0.10) from the half life of 4.54 +/- 0.71 hrs after treatment with rifampin. In the non-rifampin treated rabbits, the initial mean theophylline half life of 4.78 +/- 1.05 was not different p greater than 0.80) from the half life of 4.94 +/- 1.92 hrs after fourteen days. No significant alterations in clearance or area under the curve were noted for either group. Power analysis indicated that three rabbits were sufficient to detect at least a 25% change in the parameters as being significant (p less than 0.05).
在六只兔子中评估了单次静脉注射10mg/kg氨茶碱后茶碱的药代动力学特征。其中三只兔子每天接受50mg/kg利福平治疗,持续14天,在再次给予10mg/kg氨茶碱剂量后,对所有六只兔子的茶碱特征进行了重新评估。利福平治疗前茶碱的平均半衰期为5.11±0.71小时,与利福平治疗后的半衰期4.54±0.71小时无差异(p大于0.10)。在未接受利福平治疗的兔子中,最初茶碱的平均半衰期为4.78±1.05,与十四天后的半衰期4.94±1.92小时无差异(p大于0.80)。两组的清除率或曲线下面积均未观察到显著变化。功效分析表明,三只兔子足以检测到参数至少25%的变化具有显著性(p小于0.05)。