Hallé F, Marfil F, Sioufi A, Dubois J P, Gioud-Paquet M, Lenoir G, Prieur A M
INSERM U132, Hôpital Necker-Enfants Malades, Paris, France.
Eur J Drug Metab Pharmacokinet. 1991 Jan-Mar;16(1):29-34. doi: 10.1007/BF03189871.
Pirprofen (100 or 200 mg; Rengasil) was administered to experimental groups of children (children with juvenile chronic arthritis, JCA) and to a control group of children (children without JCA) as a single dose or as repeated doses. The pharmacokinetics of pirprofen in these children were compared to the pharmacokinetic parameter values obtained in healthy volunteers and in elderly arthritic adults receiving 400 mg of pirprofen. The children were examined regularly and laboratory values were determined in order to detect possible side effects. The results demonstrated that the pharmacokinetics of pirprofen were similar for children and adults when taking into account the dose and the body weight. There was no drug accumulation after repeated administration of pirprofen. As already observed in rheumatic adults, pirprofen remains in synovial fluid longer than in plasma.
将吡洛芬(100或200毫克;Rengasil)以单剂量或重复剂量给予实验组儿童(青少年慢性关节炎,JCA患儿)和对照组儿童(无JCA的儿童)。将这些儿童体内吡洛芬的药代动力学与健康志愿者以及接受400毫克吡洛芬的老年关节炎患者所获得的药代动力学参数值进行比较。定期对儿童进行检查,并测定实验室值以检测可能的副作用。结果表明,考虑到剂量和体重,儿童和成人吡洛芬的药代动力学相似。重复给予吡洛芬后没有药物蓄积。正如在风湿性疾病成人中已经观察到的那样,吡洛芬在滑液中的停留时间比在血浆中更长。