Helleberg L
Clin Pharmacokinet. 1981 Jul-Aug;6(4):245-58. doi: 10.2165/00003088-198106040-00001.
Indomethacin (1-(p-chlorobenzoyl)-5-methoxy-2-methylindole-3-acetic acid) is an anit-in-flammatory antipyretic drug commonly used for symptomatic relief of pain and stiffness in rheumatic diseases. Following oral administration the absorption of the drug is rapid and complete, but with important inter-and intraindividual variations. In general, peak plasma concentrations of 2 to 3 microgram/ml are achieved with 1 to 2 hours, but concomitant ingestion of food reduces and delays the peak concentrations without reducing the amount absorbed. Rectal administration is associated with earlier but lower peak plasma concentrations, incomplete absorption form suppositories, and offers no clinical advantages when compared with equivalent oral dosage. In plasma at 90% of indomethacin is bound to albumin at therapeutic plasma concentrations. Indomethacin is distributed into the synovial fluid, is excreted in human breast milk and crosses the placenta in significant amounts. It is metabolised to O-desmethylindomethacin, N-deschlorobenzoylindomethacin and O-desmethy-N-deschlorobenzoylindomethacin, which are devoid of anti-inflammatory activity and are present in significant amount in the plasma. About 60% of an oral dose is excreted in the urine predominantly in glucuronidated form, while about 40% is excreted in the faeces after biliary secretion. A large amount of the dose undergoes biliary recycling. The biotransformation is independent of the route of administration. A 2-compartment open model with correction for biliary recycling can be used to describe the disposition of indomethacin. The drug has a biological half-life of about 5 to 10 hours and a plasma clearance of 1 to 2.5ml/kg/min. In premature infants the half-life of indomethacin is inversely correlated with gestational age and is significantly prolonged as compared with adults. Renal failure does not affect the serum concentrations of indomethacin. Probenecid results in increased plasma concentrations of indomethacin with enhanced pain relief without increasing the incidence of side effects. There seem to be no significant pharmacokinetic interactions between indomethacin and aspirin or warfarin. To date it has not been possible to identify a relationship between the clinical effects and plasma concentration of indomethacin.
吲哚美辛(1-(对氯苯甲酰基)-5-甲氧基-2-甲基吲哚-3-乙酸)是一种抗炎解热药物,常用于缓解风湿性疾病中的疼痛和僵硬症状。口服后,药物吸收迅速且完全,但个体间和个体内存在重要差异。一般来说,服药1至2小时后血浆浓度峰值可达2至3微克/毫升,但同时摄入食物会降低并延迟峰值浓度,而不减少吸收量。直肠给药的血浆浓度峰值出现较早但较低,栓剂吸收不完全,与同等口服剂量相比无临床优势。在治疗血浆浓度下,吲哚美辛90%与血浆中的白蛋白结合。吲哚美辛可分布到滑液中,可在人乳中排泄,并大量穿过胎盘。它代谢为O-去甲基吲哚美辛、N-去氯苯甲酰基吲哚美辛和O-去甲基-N-去氯苯甲酰基吲哚美辛,这些代谢产物无抗炎活性,且在血浆中大量存在。口服剂量的约60%以葡萄糖醛酸化形式主要经尿液排泄,约40%经胆汁分泌后随粪便排泄。大量剂量会进行胆汁循环。生物转化与给药途径无关。可使用一个校正胆汁循环的二室开放模型来描述吲哚美辛的处置情况。该药物的生物半衰期约为5至10小时,血浆清除率为1至2.5毫升/千克/分钟。在早产儿中,吲哚美辛的半衰期与胎龄呈负相关,与成年人相比显著延长。肾衰竭不影响吲哚美辛的血清浓度。丙磺舒可使吲哚美辛的血浆浓度升高,增强止痛效果且不增加副作用发生率。吲哚美辛与阿司匹林或华法林之间似乎不存在显著的药代动力学相互作用。迄今为止,尚未确定吲哚美辛的临床效果与血浆浓度之间的关系。