STEREOSELECTIVE DISPOSITION OF ETODOLAC ENANTIOMERS IN SYNOVIAL-FLUID

被引:24
作者
BROCKS, DR
JAMALI, F
RUSSELL, AS
机构
[1] UNIV ALBERTA,FAC PHARM & PHARMACEUT SCI,EDMONTON T6G 2N8,ALBERTA,CANADA
[2] UNIV ALBERTA,FAC MED,DEPT RHEUMATOL,EDMONTON T6G 2N8,ALBERTA,CANADA
关键词
D O I
10.1002/j.1552-4604.1991.tb03770.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The synovial fluid (SF) uptake of the chiral nonsteroidal anti-inflammatory drug, etodolac, was studied in six arthritic patients, 2 hours (n = 1) or 12 hours (n = 5) after a single 200 mg dose of racemate. Marked stereoselectivity was seen in both SF and plasma; concentrations of pharmacologically inactive R-etodolac were up to 10-fold greater than active S-etodolac. Concentrations of S-etodolac were greater in SF than in plasma (SF:plasma ratio = 1.98 +/- 0.8): No such difference was seen for R-etodolac (SF:plasma = 0.91 +/- 0.3). Considerable concentrations of conjugated enantiomers were present in SF. In vitro equilibrium dialysis studies in drug-spiked samples showed that the unbound fraction of both enantiomers in SF was greater than in plasma; both fluids bound R more extensively than S etodolac. Therapeutically active S-etodolac has greater concentrations in synovial fluid than plasma during the post-distributive phase, which may be of possible clinical relevance.
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页码:741 / 746
页数:6
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