Willis J V, Kendall M J, Jack D B
Eur J Clin Pharmacol. 1980 Nov;18(5):415-8. doi: 10.1007/BF00636795.
Previous studies have shown that aspirin interacts with orally administered diclofenac sodium, causing reduced peak concentrations, lower levels and decreased areas under curves. In this study, diclofenac sodium was administered orally and intravenously with and without aspirin, to 6 healthy female volunteers. After intravenous dosing both plasma levels and areas under curves were significantly reduced although none of the rate constants was affected. The volume of distribution of diclofenac was increased as was the plasma clearance. Oral administration with aspirin also resulted in lower plasma levels, particularly peak levels, and areas under curves. Comparison of AUC's for both modes of administration with and without aspirin suggested that lower levels after oral administration were not due to impaired absorption. These observations are best explained by decreased protein binding and increased biliary excretion of diclofenac in the presence of salicylate.
先前的研究表明,阿司匹林与口服双氯芬酸钠相互作用,导致峰值浓度降低、水平降低以及曲线下面积减小。在本研究中,对6名健康女性志愿者口服和静脉注射双氯芬酸钠,同时使用和不使用阿司匹林。静脉给药后,尽管速率常数均未受影响,但血浆水平和曲线下面积均显著降低。双氯芬酸的分布容积增加,血浆清除率也增加。与阿司匹林一起口服给药也导致血浆水平降低,尤其是峰值水平以及曲线下面积减小。对使用和不使用阿司匹林的两种给药方式的曲线下面积进行比较表明,口服给药后水平降低并非由于吸收受损。这些观察结果最好的解释是在水杨酸盐存在的情况下双氯芬酸的蛋白结合减少和胆汁排泄增加。