Awni W M, Cavanaugh J H, Tzeng T B, Witt G, Granneman G R, Dubé L M
Pharmacokinetics and Biopharmaceutics Department, Abbott Laboratories, Abbott Park, Illinois, USA.
Clin Pharmacokinet. 1995;29 Suppl 2:105-11. doi: 10.2165/00003088-199500292-00015.
A randomized double-blind placebo-controlled crossover study evaluated the effects of zileuton 600mg 4 time daily on the pharmacokinetics of prednisolone after a single 400mg oral dose of prednisone. the effects of the single prednisone dose on the steady-state pharmacokinetics of zileuton were also evaluated. Multiple doses of zileuton had no significant effects on mean peak plasma concentration (Cmax), time to Cmax(tmax), or area under the plasma concentration-time curve from 0 to infinity (AUC0-infinity) values for prednisolone after oral administration of prednisone 40mg. A slight but statistically significant increase in the mean half-life (t1/2) of prednisolone was detected with zileuton + prednisone administration compared with prednisone + placebo (from 2.8 to 2.9 hours); however, this change was of no clinical relevance. Mean Cmax values of zileuton after coadministration with prednisone were similar to those of zileuton alone. While the single 40mg dose of prednisone resulted in a slight but statistically significant decrease in the mean zileuton AUC value from 0 to 6 hours (AUC0-6) [from 23 to 20 mg/L/h] and a reduction in tMAX (from 2.3 to 1.7 hours), these results were not considered to be clinically significant. Therefore, it is considered that zileuton and prednisone may be coadministered with minimal risk of a clinically significant pharmacokinetic interaction.
一项随机双盲安慰剂对照交叉研究评估了每日4次服用600mg齐留通对单次口服400mg泼尼松后泼尼松龙药代动力学的影响。还评估了单次泼尼松剂量对齐留通稳态药代动力学的影响。多次服用齐留通对口服40mg泼尼松后泼尼松龙的平均血浆峰浓度(Cmax)、达峰时间(tmax)或血浆浓度-时间曲线下从0至无穷大的面积(AUC0-无穷大)值均无显著影响。与泼尼松+安慰剂相比,齐留通+泼尼松联合给药时检测到泼尼松龙的平均半衰期(t1/2)有轻微但具有统计学意义的增加(从2.8小时增至2.9小时);然而,这一变化无临床相关性。齐留通与泼尼松合用时的平均Cmax值与单独使用齐留通时相似。虽然单次40mg剂量的泼尼松导致齐留通从0至6小时的平均AUC值(AUC0-6)有轻微但具有统计学意义的降低[从23降至20mg/L/h]以及tMAX缩短(从2.3小时降至1.7小时),但这些结果不被认为具有临床意义。因此,认为齐留通和泼尼松联合给药时发生具有临床意义的药代动力学相互作用的风险极小。