Hobbs D C, Twomey T M
J Clin Pharmacol. 1979 May-Jun;19(5-6):270-81. doi: 10.1002/j.1552-4604.1979.tb02480.x.
Pharmacokinetic studies with piroxicam, a nonsteroidal antiinflammatory agent, have been carried out following the administration of single and multiple oral doses. A plasma half-life of approximately 45 hours is observed, permitting the use of single daily doses in therapy. Enterohepatic recirculation of drug is suggested by the presence of multiple peaks in plasma concentration curves. Piroxicam is highly bound to serum proteins. The absorption and disposition of piroxicam are unaffected by the concomitant administration of aspirin and antiacids. Salicylate plasma levels are similarly unaffected by piroxicam administration.
对非甾体抗炎药吡罗昔康进行了单次和多次口服给药后的药代动力学研究。观察到血浆半衰期约为45小时,这使得在治疗中可以每日单次给药。血浆浓度曲线中出现多个峰表明存在药物的肠肝循环。吡罗昔康与血清蛋白高度结合。同时服用阿司匹林和抗酸剂不影响吡罗昔康的吸收和处置。服用吡罗昔康也同样不影响水杨酸盐的血浆水平。