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托美丁及其代谢产物在大鼠和小鼠个体血浆中的时间进程。

The time course of tolmetin and its metabolites in the plasma of individual rats and mice.

作者信息

Migdalof B H, Yorgey K A, Popkave C G

出版信息

Drug Metab Dispos. 1976 Sep-Oct;4(5):468-73.

PMID:10146
Abstract

Tolmetin, 1-methyl-(5-p-toluoyl)pyrrole-2-acetic acid, is a new, nonsteroidal, anti-inflammatory agent. After oral administration of tolmetin-14C to rats and mice, sequential microsamples of blood were obtained from the ophthalmic venous plexus via the orbital sinus. Plasma was collected after centrifugation, and microaliquots of each plasma sample were analyzed. The total radioactivity and thin-layer chromatographic assays used permitted quantitation of tolmetin, its dicarboxylic acid metabolite, and (by difference) all other metabolites collectively for each sample. Time-course data on plasma levels were obtained for individual rats and mice. The plasma elimination half-life of tolmetin was estimated at 0.67 +/- 0.13 hr (mean +/- SD) in male rats, 1.4 +/- 0.6 hr in female rats, 1.2 +/- 0.3 hr in male mice, and 1.0 +/- 0.0 hr in female mice. A one-compartment open model was used.

摘要

托美丁,即1-甲基-(5-对甲苯甲酰基)吡咯-2-乙酸,是一种新型非甾体抗炎药。给大鼠和小鼠口服14C标记的托美丁后,通过眶窦从眼静脉丛采集连续的微量血样。离心后收集血浆,并对每个血浆样品的微量等分试样进行分析。所采用的总放射性和薄层色谱分析方法能够对每个样品中的托美丁、其二羧酸代谢物以及(通过差值计算)所有其他代谢物进行定量。获得了个别大鼠和小鼠血浆水平的时程数据。托美丁在雄性大鼠中的血浆消除半衰期估计为0.67±0.13小时(平均值±标准差),雌性大鼠为1.4±0.6小时,雄性小鼠为1.2±0.3小时,雌性小鼠为1.0±0.0小时。采用一室开放模型。

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