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Interaction of isoxicam with acetylsalicylic acid.

机译:异西康与乙酰水杨酸的相互作用。

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摘要

Ten healthy male volunteers were given 200 mg p.o. of isoxicam after an overnight fast and the plasma concentrations over time followed for 96 h by h.p.l.c. Five days later enteric coated acetylsalicylic acid (ASA) 650 mg four times daily was started and continued for 10 days producing steady state trough plasma salicylate of 83 mg/l (range 21-133). A second 200 mg isoxicam dose was given 5 days after starting ASA and the plasma concentration time-curve again followed. After ASA, there was no change in lag time (0.54 vs 0.51 h), time to peak concentration (10 vs 10 h), or disappearance t1/2 (28.7 vs 31.0 h) however the peak isoxicam concentration and AUC were reduced 18 and 22% respectively (P less than 0.01). Plasma protein binding of isoxicam studied by equilibrium dialysis was 96 +/- 1% in the absence and 86 +/- 5% in the presence of ASA. The reduction in binding was unrelated to plasma SA concentrations achieved or observed reductions in AUC for plasma isoxicam. ASA decreased plasma isoxicam binding, peak plasma isoxicam concentrations and AUC without altering the apparent disappearance half-life of total plasma isoxicam after a single oral dose.
机译:十名健康的男性志愿者口服200 mg。禁食过夜后,立即用异丙酚进行h.p.l.c处理96小时。五天后,开始每天四次650 mg的肠溶衣衣的乙酰水杨酸(ASA),并持续10天,产生83 mg / l(范围21-133)的稳态谷水杨酸盐血浆。在开始ASA后5天给予第二次200 mg异昔康酮剂量,然后再次进行血浆浓度时间曲线。 ASA后,滞后时间(0.54 vs 0.51 h),到达峰浓度的时间(10 vs 10 h)或t1 / 2消失(28.7 vs 31.0 h)没有变化,但是异昔康酮的峰浓度和AUC降低了18和分别为22%(P小于0.01)。在不存在透析的情况下通过平衡透析研究的异昔康血浆蛋白结合率是96 +/- 1%,在存在ASA的情况下是86 +/- 5%。结合的减少与所达到的血浆SA浓度无关,或者观察到血浆异昔康的AUC减少。 ASA降低了血浆异西cam的结合,血浆血浆异西cam的峰值浓度和AUC,而没有改变单次口服后总血浆异昔康的表观消失半衰期。

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