Rossi F A, Ferrero M, Balladore G E, Zecca L, Fraschini F, Ferrario P, Bichisao E, Monza G C, Maresca V
Center of Rheumatology, USSL 11, Genova, Italy.
Eur J Clin Pharmacol. 1988;35(4):379-83. doi: 10.1007/BF00561368.
Plasma concentrations of pirprofen and of its pyrrol metabolite were assessed in 9 elderly patients (3 males, 6 females; mean age 76 years) suffering from chronic degenerative disease. Pirprofen 400 mg in 4 ml was administered i.m. and the pharmacokinetic profile of the drug and the metabolite was calculated. The AUC, Cmax and t1/2 of pirprofen were similar to those found in previous studies, and, as expected, those parameters for the pyrrol metabolite were lower (Cmax = 2.8 micrograms/ml-1; tmax = 6.4 h; AUC(0-32) = 56.5 micrograms.h.ml-1). One patient (n = 8) showed different pharmacokinetic behaviour, which is discussed. The data suggest that age has little influence on the pharmacokinetic of pirprofen, although unpredictable responses should always be considered in clinical practice.
对9例患有慢性退行性疾病的老年患者(3例男性,6例女性;平均年龄76岁)的血浆吡洛芬及其吡咯代谢物浓度进行了评估。将400毫克吡洛芬溶于4毫升溶液中进行肌肉注射,并计算该药物及其代谢物的药代动力学曲线。吡洛芬的AUC、Cmax和t1/2与先前研究中的结果相似,并且正如预期的那样,吡咯代谢物的这些参数较低(Cmax = 2.8微克/毫升-1;tmax = 6.4小时;AUC(0 - 32) = 56.5微克·小时·毫升-1)。1例患者(n = 8)表现出不同的药代动力学行为,对此进行了讨论。数据表明,年龄对吡洛芬的药代动力学影响较小,尽管在临床实践中应始终考虑不可预测的反应。