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萘丁美酮在马体内的活性代谢物6-甲氧基-2-萘乙酸的处置与排泄

Disposition and excretion of 6-methoxy-2-naphthylacetic acid, the active metabolite of nabumetone in horses.

作者信息

Soma L R, Uboh C E, Rudy J A, Smith M S

机构信息

School of Veterinary Medicine, University of Pennsylvania 19348, USA.

出版信息

Am J Vet Res. 1996 Apr;57(4):517-21.

PMID:8712517
Abstract

OBJECTIVE

To examine, in horses, the disposition and excretion of the active metabolite 6-methoxy-2-naphthylacetic acid (6MNA) of the nonsteroidal anti-inflammatory prodrug nabumetone.

DESIGN

Pharmacokinetic analysis of 6MNA after oral administration of nabumetone and IV administration of 6MNA.

PROCEDURE

Using a crossover design, 5 horses were orally administered 3.7 mg of nabumetone/kg of body weight. After a 3-week washout period, 4 horses were administered 2.5 mg of 6MNA/kg, IV.

RESULTS

Absorption of nabumetone from the gastrointestinal tract and its metabolism to 6MNA had a median appearance half-life of 0.88 hour. The elimination half-life was 11 hours. Area under the plasma concentration time curve for 6MNA after oral administration of nabumetone was 120.6 mg/h/L. A dose of 2.5 mg/kg of 6MNA administered IV resulted in plasma concentration nearly equivalent to that induced by the orally administered dose. Disposition of 6MNA was modeled as a one-compartment, first-order elimination. The area under the plasma concentration time curve for IV administration of 6MNA was 117.0 mg/h/L, and the specific volume of distribution was 0.247 L/kg. The distribution half-life and the elimination half-life were 0.56 and 7.90 hours, respectively. Percentage of total dose recovered in urine for the 36-hour collection period after the oral and IV administrations was 7.4 and 5.3%, respectively.

CONCLUSIONS

Metabolism of nabumetone to 6MNA, as reported in other species, also occurs in horses. There were a number of additional metabolites of nabumetone in urine that could not be fully identified and characterized.

摘要

目的

研究非甾体抗炎前体药物萘丁美酮的活性代谢产物6-甲氧基-2-萘乙酸(6MNA)在马体内的处置和排泄情况。

设计

口服萘丁美酮及静脉注射6MNA后对6MNA进行药代动力学分析。

步骤

采用交叉设计,给5匹马口服3.7毫克/千克体重的萘丁美酮。经过3周的洗脱期后,给4匹马静脉注射2.5毫克/千克的6MNA。

结果

萘丁美酮从胃肠道的吸收及其代谢为6MNA的中位出现半衰期为0.88小时。消除半衰期为11小时。口服萘丁美酮后6MNA的血浆浓度-时间曲线下面积为120.6毫克/小时/升。静脉注射2.5毫克/千克的6MNA所产生的血浆浓度几乎等同于口服该剂量所诱导的血浆浓度。6MNA的处置被模拟为单室一级消除。静脉注射6MNA的血浆浓度-时间曲线下面积为117.0毫克/小时/升,比分布容积为0.247升/千克。分布半衰期和消除半衰期分别为0.56小时和7.90小时。口服和静脉注射后36小时收集期内尿液中回收的总剂量百分比分别为7.4%和5.3%。

结论

如在其他物种中所报道的,萘丁美酮代谢为6MNA在马体内也会发生。尿液中还有一些萘丁美酮的其他代谢产物无法完全鉴定和表征。

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