Milne G M, Twomey T M
Agents Actions. 1980 Apr;10(1 Pt 2):31-7. doi: 10.1007/BF02024176.
In animal antinociceptive tests responsive to non-steroidal anti-inflammatory drugs (NSAID), piroxicam is an extremely potent and effective analgetic at doses of 1--2 mg/kg p.o. In mice the plasma half-life and duration of analgetic action is short (t 1/2 = 1.7 h), unlike man, wherein piroxicam exhibits an exceptionally long duration of action (half-life 40--45 h). An excellent correlation is observed between plasma levels and analgetic activity in the writhing test in mice suggesting that piroxicam will exhibit potent and long-lasting analgetic activity in man.
在对非甾体抗炎药(NSAID)有反应的动物抗伤害感受测试中,吡罗昔康在口服剂量为1-2mg/kg时是一种极其强效且有效的镇痛药。与人类不同,小鼠体内吡罗昔康的血浆半衰期和镇痛作用持续时间较短(t1/2 = 1.7小时),而在人类中吡罗昔康表现出异常长的作用持续时间(半衰期40-45小时)。在小鼠扭体试验中观察到血浆水平与镇痛活性之间具有良好的相关性,这表明吡罗昔康在人体内将表现出强效且持久的镇痛活性。