Blocka K L, Richardson C J, Wallace S M, Ross S G, Verbeeck R K
College of Medicine and Pharmacy, University of Saskatchewan, Saskatoon, Canada.
J Rheumatol. 1988;15(5):757-63.
The disposition of piroxicam in 23 patients with rheumatoid arthritis (9 males, 14 females, aged 27-79) was studied over 6 weeks using the standard oral dose of 20 mg daily. Clinical status was monitored using standard methods. The mean piroxicam steady state plasma concentration (Css) averaged 9.2 +/- 4.4 micrograms/ml, the majority of which was highly protein bound (1.4 +/- 0.5% unbound). Total plasma clearance (CL/F) of piroxicam was 1.85 +/- 0.81 ml/min and the half life (t1/2) was 53.0 +/- 24.2 h. There was wide intersubject variability in the kinetics of piroxicam and its major metabolite 5'-hydroxypiroxicam. Piroxicam CL/F, t1/2 and Css were modestly correlated with patient age. Clinical effects did not appear to be related to piroxicam plasma levels.
对23名类风湿性关节炎患者(9名男性,14名女性,年龄27 - 79岁)进行了为期6周的研究,采用每日20毫克的标准口服剂量,观察吡罗昔康的处置情况。使用标准方法监测临床状态。吡罗昔康的平均稳态血浆浓度(Css)平均为9.2±4.4微克/毫升,其中大部分与蛋白质高度结合(未结合部分为1.4±0.5%)。吡罗昔康的总血浆清除率(CL/F)为1.85±0.81毫升/分钟,半衰期(t1/2)为53.0±24.2小时。吡罗昔康及其主要代谢物5'-羟基吡罗昔康的动力学在受试者之间存在很大差异。吡罗昔康的CL/F、t1/2和Css与患者年龄呈适度相关。临床效果似乎与吡罗昔康的血浆水平无关。