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比格犬体内[14C]-环氯噻嗪的组织分布及在尿液、粪便和呼出二氧化碳中的排泄情况

Tissue distribution and excretion in urine, feces and respiratory CO2 of [14C]-ciclosidomine in beagle dogs.

作者信息

Matteo M R, Zavorskas P, Esber H

出版信息

Arzneimittelforschung. 1985;35(1A):329-32.

PMID:3921036
Abstract

14C-Labelled N-cyclohexanecarbonyl-3-(4-morpholino)-sydnone-imine hydrochloride [( 14C]-ciclosidomine, Neopres) labelled in the sydnone or morpholine position was administered orally and by intravenous injection to beagle dogs at a dose level of 1 mg/kg. The rates and routes of excretion of radioactivity were determined. The oral dose was completely absorbed and most (greater than 70%) of the radioactive label (both positions) was excreted in the urine within the first 24-48 h. The remaining label(morpholine-labelled drug) was found in feces (less than or equal to 8%), respiratory 14CO2 (2.3%) and throughout the carcass, with no major single depot. Radioactivity peaked within four hours. Elimination of dose label from the blood was biphasic, with an alpha phase (t 1/2 of 2.5 and 4.6 h after oral administration of morpholine- and sydnone-labelled drug, respectively) and a very slow beta-phase (t 1/2 = 120 h, both labels). Thin layer chromatography of 0-24 h urines (morpholine label) indicated total metabolism of the parent compound. A device is described for the continuous monitoring over several days of 14CO2 in exhaled breath from a conscious dog.

摘要

将标记于西多胺或吗啉位置的14C标记的N-环己烷羰基-3-(4-吗啉基)-西多酮亚胺盐酸盐[(14C]-西氯司明,Neopres)以1mg/kg的剂量水平口服和静脉注射给予比格犬。测定放射性的排泄速率和途径。口服剂量被完全吸收,大部分(超过70%)放射性标记(两个位置)在最初的24 - 48小时内随尿液排出。其余的标记物(吗啉标记的药物)在粪便中发现(小于或等于8%)、呼吸道排出的14CO2(2.3%)以及整个胴体中,没有主要的单一储存部位。放射性在4小时内达到峰值。血液中剂量标记物的消除呈双相,α相(分别在口服吗啉标记和西多胺标记的药物后,t 1/2为2.5小时和4.6小时)和非常缓慢的β相(t 1/2 = 120小时,两种标记物)。0 - 24小时尿液(吗啉标记)的薄层色谱显示母体化合物完全代谢。描述了一种用于连续几天监测清醒犬呼出气体中14CO2的装置。

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