Caruso I, Corvi G, Fuccella L M, Moro E, Sacchetti G, Tamassia V, Tosolini G P
Int J Clin Pharmacol Biopharm. 1977 Sep;15(9):411-6.
The pharmacokinetics of indoprofen in healthy subjects after single oral and i.v. administrations is reviewed. During repeated administration of indoprofen to 6 normal subjects (200-mg tablet every 8 hours for 6 days) no variations in the disposition of the drug were found in comparison with single dose administration. In 6 inpatients, with rheumatoid arthritis, the pharmacokinetics of indoprofen was studied after single oral (tablet) and i.m. administration. As for oral doses, no difference in main kinetic parameters was detected between the patients and normal subjects except for a higher volume of distribution in the former population. The bioavailability of the drug given by i.m. injection was not significantly different from that observed after oral administration.
本文综述了健康受试者单次口服和静脉注射吲哚美辛后的药代动力学。在对6名正常受试者重复给药吲哚美辛(每8小时服用200毫克片剂,共6天)期间,与单次给药相比,未发现药物处置有变化。在6名类风湿性关节炎住院患者中,研究了单次口服(片剂)和肌肉注射吲哚美辛后的药代动力学。对于口服剂量,除了前者人群的分布容积较高外,患者和正常受试者之间的主要动力学参数未检测到差异。肌肉注射给药的药物生物利用度与口服给药后观察到的生物利用度无显著差异。