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血浆和滑液中的萘普生浓度及其对类前列腺素浓度的影响。

Naproxen concentrations in plasma and synovial fluid and effects on prostanoid concentrations.

作者信息

Day R O, Francis H, Vial J, Geisslinger G, Williams K M

机构信息

Department of Clinical Pharmacology and Toxicology, University of New South Wales, Sydney, Australia.

出版信息

J Rheumatol. 1995 Dec;22(12):2295-303.

PMID:8835565
Abstract

OBJECTIVE

To test the hypothesis that unbound concentrations of naproxen in synovial fluid (SF) and plasma (P) are equal over a drug dosage interval at steady state or after a single dose of drug. The relationship between plasma and SF concentrations of naproxen, respectively, and prostaglandin concentrations were also examined.

METHODS

Paired, sequential, total, and unbound naproxen concentrations were determined in plasma and SF in 2 groups of 6 patients. A single dose group was given naproxen 500 mg. The chronic dose group was given 500 mg bd for 7 days before collection of blood and SF samples. The effect of naproxen on prostanoid production by clotting whole blood (thromboxane B2, TXB2) and in SF (PGE2, 6-keto-PGF1 alpha) was determined by radioimmunoassay.

RESULTS

Average area under the curve (AUC) of unbound (U) naproxen concentrations against time in plasma and SF were the same over a dosage interval at steady state (ratio AUCU,SF/AUCU,P, 1.12 +/- 0.18; p = 0.108), but not after a single acute dose (AUCU,SF/AUCU,P, 1.34 +/- 0.32; p = 0.044). Data from the single dose study revealed that the mean (+/- SD) of the concentrations required for 50% inhibition (EC50) of platelet derived TXB2 by total naproxen was 7.7 +/- 4.4 micrograms/ml (n = 5) and for unbound drug 25.4 +/- 22.0 ng/ml (n = 5). SF prostanoid concentrations after both acute and chronic dosing were low, as expected, but temporal and dose relationships of prostanoid concentrations with SF naproxen could not be discerned. However, this may reflect study design.

CONCLUSIONS

The AUC of unbound naproxen in SF and plasma were similar at steady state. Plasma concentrations correlated with inhibition of TXB2 generation by platelets. There was sustained depression of PG concentrations in SF beyond the time suggested by plasma drug concentrations.

摘要

目的

验证在稳态给药间隔期或单剂量给药后,滑液(SF)和血浆(P)中萘普生的游离浓度相等这一假设。同时还研究了萘普生血浆浓度与SF浓度分别和前列腺素浓度之间的关系。

方法

对两组各6名患者的血浆和SF中的萘普生进行配对、连续、总浓度和游离浓度测定。单剂量组给予萘普生500mg。慢性剂量组在采集血液和SF样本前7天,每天两次给予500mg。通过放射免疫分析法测定萘普生对全血凝血产生前列腺素(血栓素B2,TXB2)以及在SF中(前列腺素E2,6-酮-前列腺素F1α)的影响。

结果

在稳态给药间隔期,血浆和SF中游离萘普生浓度随时间变化的平均曲线下面积(AUC)相同(游离萘普生浓度AUCU,SF/AUCU,P的比值为1.12±0.18;p = 0.108),但在单次急性给药后不同(AUCU,SF/AUCU,P,1.34±0.32;p = 0.044)。单剂量研究数据显示,总萘普生对血小板衍生TXB2产生50%抑制作用(EC50)所需浓度的平均值(±标准差)为7.7±4.4μg/ml(n = 5),游离药物为25.4±22.0ng/ml(n = 5)。正如预期的那样,急性和慢性给药后SF中前列腺素浓度均较低,但无法辨别前列腺素浓度与SF中萘普生的时间和剂量关系。然而,这可能反映了研究设计问题。

结论

稳态时SF和血浆中游离萘普生的AUC相似。血浆浓度与血小板TXB2生成的抑制相关。SF中PG浓度的持续降低时间超过血浆药物浓度所提示的时间。

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