Nichol F E, Samanta A, Rose C M
Department of Rheumatology, Leicester Royal Infirmary.
Drugs. 1988;35 Suppl 1:46-51. doi: 10.2165/00003495-198800351-00010.
Tiaprofenic acid is a potent non-steroidal anti-inflammatory drug which, in conventional tablet form, has been shown to be rapidly absorbed and eliminated from the plasma, while synovial fluid concentrations remain constant for at least 8 hours. Recently, a sustained action formulation of tiaprofenic acid has been developed to provide the patient with the convenience of a once daily dosage. The purpose of this study was to measure plasma and synovial fluid concentrations over a 24-hour period following repeated administration of the sustained action formulation, and thus determine the pharmacokinetic profile. Eight patients suffering from rheumatoid arthritis were included in this open study (of whom 3 were subsequently excluded from the analysis). All were hospital outpatients requiring aspiration of the knee joint. The patients received sustained action tiaprofenic acid in a dosage of 600 mg once daily for a period of 7 days. Plasma and synovial fluid samples were taken on the final treatment day at 0, 4, 8, 12, and 18 hours following administration of the last treatment dose. Areas under the concentration-time curves, maximum plasma and synovial fluid concentrations, times to maximum concentration, and apparent elimination half-lives are presented and the findings compared and discussed. The drug was found to be retained in both the plasma and synovial fluid over a 24-hour period. Synovial fluid concentrations exceeded plasma concentrations at 24 hours in 4 of the 5 patients who were analysed, while in the fifth patient the levels were very similar.
噻洛芬酸是一种强效非甾体抗炎药,其传统片剂形式已被证明能迅速从血浆中吸收和消除,而滑液浓度至少在8小时内保持恒定。最近,已开发出噻洛芬酸的缓释制剂,为患者提供每日一次给药的便利。本研究的目的是在重复给予缓释制剂后的24小时内测量血浆和滑液浓度,从而确定药代动力学特征。本开放性研究纳入了8名类风湿性关节炎患者(其中3名随后被排除在分析之外)。所有患者均为需要抽取膝关节液的医院门诊患者。患者接受剂量为600 mg的噻洛芬酸缓释制剂,每日一次,为期7天。在最后一个治疗日,于最后一剂治疗药物给药后的0、4、8、12和18小时采集血浆和滑液样本。给出了浓度-时间曲线下面积、最大血浆和滑液浓度、达到最大浓度的时间以及表观消除半衰期,并对结果进行了比较和讨论。结果发现,该药物在24小时内保留在血浆和滑液中。在分析的5名患者中,有4名患者在24小时时滑液浓度超过血浆浓度,而在第5名患者中,两者水平非常相似。