Kraml M, Hicks D R, McKean M, Panagides J, Furst D
Ayerst Laboratories Research, New York, N.Y.
Clin Pharmacol Ther. 1988 May;43(5):571-6. doi: 10.1038/clpt.1988.75.
The pharmacokinetics of etodolac have been evaluated in five patients with arthritis given 200 mg etodolac, twice daily, at 12-hour intervals, for 7 days. Albumin and total protein concentrations were markedly lower in synovial fluid than in serum, and etodolac free fraction was significantly higher. Etodolac readily penetrated into the synovial fluid, and in the postdistributive phase the concentration of free etodolac (i.e., the drug responsible for pharmacologic activity) remained higher than that in serum at all times. No differences in the half-life of etodolac elimination were noted.
已对5名关节炎患者进行了依托度酸的药代动力学评估,这些患者每天两次、每隔12小时服用200 mg依托度酸,共服用7天。滑液中的白蛋白和总蛋白浓度明显低于血清中的浓度,依托度酸的游离分数显著更高。依托度酸很容易渗透到滑液中,在分布后阶段,游离依托度酸(即具有药理活性的药物)的浓度在所有时间均高于血清中的浓度。未观察到依托度酸消除半衰期的差异。