Mojaverian P, Rocci M L, Swanson B N, Vlasses P H, Chremos A N, Lin J H, Yeh J C, Ferguson R K
Pharmacotherapy. 1985 Nov-Dec;5(6):336-9. doi: 10.1002/j.1875-9114.1985.tb03440.x.
To evaluate the steady-state bioequivalence of the nonsteroidal antiinflammatory analgesic agent, diflunisal, administered once versus twice daily, 13 healthy volunteers received diflunisal as follows: 1000 mg at 8:00 AM and 500 mg at 8:00 AM and 8:00 PM, each for 14 days in a randomized crossover study. The mean (+/- SD) steady-state peak plasma concentrations were significantly greater after once-daily dosing (186 +/- 25 micrograms/ml vs 150 +/- 37 micrograms/ml; p less than 0.01). The time to peak concentration was also longer after the single-dose regimen (2.5 +/- 0.8 vs 1.9 +/- 0.9 hr; p less than 0.05). The regimens were similar with respect to the mean 24-hour area under the plasma concentration-time curve at steady state (2839 +/- 612 vs 2782 +/- 778 micrograms.hr.ml-1), steady-state plasma concentrations (118 +/- 25 vs 116 +/- 32 micrograms/ml), trough plasma concentration (85 +/- 27 vs 92 +/- 28 micrograms/ml) as well as 24-hour urinary excretion (776 +/- 79 vs 771 +/- 89 mg) of diflunisal. Based on urinary recoveries, the bioequivalence ratio (once vs twice daily) was 1.01 +/- 0.08. These results indicate that diflunisal administered once daily might offer comparable therapeutic effects but be more convenient than a twice-daily regimen.
为评估非甾体抗炎镇痛药双氟尼酸每日给药一次与每日给药两次的稳态生物等效性,13名健康志愿者接受了如下双氟尼酸给药:上午8:00服用1000毫克,以及上午8:00和晚上8:00各服用500毫克,在一项随机交叉研究中,每种给药方式各持续14天。每日一次给药后的平均(±标准差)稳态血药峰浓度显著更高(186±25微克/毫升对150±37微克/毫升;p<0.01)。单剂量给药方案后的达峰时间也更长(2.5±0.8对1.9±0.9小时;p<0.05)。两种给药方案在稳态时血浆浓度-时间曲线下的平均24小时面积(2839±612对2782±778微克·小时·毫升⁻¹)、稳态血浆浓度(118±25对116±32微克/毫升)、谷血浆浓度(85±27对92±28微克/毫升)以及双氟尼酸的24小时尿排泄量(776±79对771±89毫克)方面相似。基于尿回收率,生物等效比(每日一次对每日两次)为1.01±0.08。这些结果表明,每日一次给药的双氟尼酸可能具有相当的治疗效果,但比每日两次给药方案更方便。