Tenconi L T, Buniva G, Beretta E, Pagani V
Int J Clin Pharmacol Biopharm. 1977 Oct;15(10):485-91.
An average 2.2-fold increase in the peak plasma concentrations of the non-steroidal anti-inflammatory agent diftalone in the presence of food was observed in three studies carried out with healthy volunteers who received an oral dose of 0.75 g (6 subjects, study 1), 0.25 g (10 subjects, study II) and 0.5 g (6 subjects, study V) of the compound at 9:00 a.m. both in fasting conditions and after a meal. The effect does not depend on the unusual time (8:00 a.m., selected for experimental needs) at which the subjects were given the meal. In fact, a 2.5-fold increase in plasma concentrations was observed when an oral dose of 0.75 g of diftalone was administered to 2 subjects (study II) both at 8:00 a.m. in fasting conditions and at 1:00 p.m. after a meal. A similar enhancement in the absorption of diftalone was observed when 5 healthy volunteers (study VI) received an oral dose of 0.5 g of the compound both as plain capsules and as capsules containing dry ox bile. However, the absorption of diftalone was not modified when the compound was administered orally as an aqueous suspension or in tensioactive vehicles, or after 20 mg of metoclopramide (study II). Also, the results of a study (IV) on 2 subjects partly deprived of bile after surgery, showed that diftalone does not undergo enterohepatic circulation. The hypothesis that the increase in diftalone absorption is mainly due to bile flow following food intake is supported by all the above experimental results.
在三项针对健康志愿者开展的研究中,观察到非甾体抗炎药双他氯灭酸在进食情况下的血浆峰值浓度平均升高了2.2倍。这些志愿者于上午9点分别在空腹和进食后口服0.75克(研究I,6名受试者)、0.25克(研究II,10名受试者)和0.5克(研究V,6名受试者)该化合物。这种影响并不取决于受试者进食的不寻常时间(为实验需要选定的上午8点)。实际上,在空腹条件下上午8点以及进食后下午1点对2名受试者(研究II)口服0.75克双他氯灭酸时,观察到血浆浓度升高了2.5倍。当5名健康志愿者(研究VI)口服0.5克该化合物的普通胶囊和含干牛胆汁的胶囊时,也观察到双他氯灭酸的吸收有类似增强。然而,当该化合物以水混悬液或在表面活性剂载体中口服给药时,或在给予20毫克甲氧氯普胺后给药时(研究II),双他氯灭酸的吸收未发生改变。此外,一项针对2名术后部分胆汁缺乏受试者的研究(研究IV)结果表明,双他氯灭酸不会进行肠肝循环。上述所有实验结果均支持双他氯灭酸吸收增加主要归因于进食后胆汁流动的假说。