Suppr超能文献

萘普生在马体内的血浆和滑液动力学、处置及尿排泄

Plasma and synovial fluid kinetics, disposition, and urinary excretion of naproxen in horses.

作者信息

Soma L R, Uboh C E, Rudy J A, Perkowski S Z

机构信息

New Bolton Center School of Veterinary Medicine, University of Pennsylvania, Kennett Square 19348, USA.

出版信息

Am J Vet Res. 1995 Aug;56(8):1075-80.

PMID:8533980
Abstract

Naproxen (+6-methoxy-[alpha-methyl]-2-naphthalene acetic acid) is a nonsteroidal anti-inflammatory drug that is used for the treatment of inflammatory conditions in horses. We developed a model that describes the drug's disposition and renal excretion, including synovial fluid disposition and elimination after IV administration in horses. The plasma disposition, after IV administration of 5 mg/kg of body weight, was described by a two-compartment model; mean +/- SD distribution and elimination half-lives were 1.42 +/- 0.42 and 8.26 +/- 2.56 hours, respectively. Plasma concentration of naproxen after IV administration of 5 mg/kg was 55.3 +/- 13.5 and 0.61 +/- 0.42 mg/L at 5 minutes and 48 hours after its administration, respectively. Steady-state volume of distribution was 0.163 +/- 0.053 L/kg, and area under the plasma concentration time-curve was 372.1 +/- 128.2 mg/h/L. The peak synovial fluid concentration of 12.68 +/- 12.39 mg/L was measured at 6 hours, and decreased to 0.71 +/- 0.38 mg/L at 36 hours after naproxen administration. The decrease of naproxen concentration in synovial fluid paralleled that in plasma. The appearance half-life of naproxen in synovial fluid was 4.64 hours, and the elimination half-life was 6.73 hours. Total body clearance was 0.015 +/- 0.006 L/h/kg. The percentage of plasma protein binding was 97.0 +/- 2.9% at plasma concentrations between 5 and 100 mg/L. This was significantly (P < 0.05) higher than the percentage of binding at plasma concentrations of 0.5, 1, and 500 mg/L, which was 75.2 +/- 11.8%. Most of the drug was excreted as glucuronidated naproxen and unconjugated desmethylnaproxen.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

萘普生(+6-甲氧基-[α-甲基]-2-萘乙酸)是一种非甾体抗炎药,用于治疗马匹的炎症性疾病。我们建立了一个模型来描述该药物的处置和肾排泄情况,包括静脉注射后在马匹中的滑液处置和消除情况。静脉注射5mg/kg体重后,血浆处置情况用二室模型描述;平均±标准差分布半衰期和消除半衰期分别为1.42±0.42小时和8.26±2.56小时。静脉注射5mg/kg后,萘普生在给药后5分钟和48小时的血浆浓度分别为55.3±13.5mg/L和0.61±0.42mg/L。稳态分布容积为0.163±0.053L/kg,血浆浓度-时间曲线下面积为372.1±128.2mg/h/L。萘普生给药后6小时测得滑液峰值浓度为12.68±12.39mg/L,36小时降至0.71±0.38mg/L。滑液中萘普生浓度的下降与血浆中平行。萘普生在滑液中的出现半衰期为4.64小时,消除半衰期为6.73小时。全身清除率为0.015±0.006L/h/kg。在血浆浓度为5至100mg/L时,血浆蛋白结合率为97.0±2.9%。这显著(P<0.05)高于血浆浓度为0.5、1和500mg/L时的结合率,后者为75.2±11.8%。大部分药物以葡萄糖醛酸化萘普生和未结合的去甲基萘普生形式排泄。(摘要截短至250字)

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验