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美沙酮在大鼠体内的胃肠道吸收。

The gastrointestinal absorption of methadone in the rat.

作者信息

Walsh C T, Levine R R, Squires C

出版信息

Drug Metab Dispos. 1975 Nov-Dec;3(6):525-9.

PMID:1229
Abstract

The absorption of dl-methadone from the gastrointestinal tract of the Sprague-Dawley rat was examined by the in vivo segment technique. Duodenal absorption, measured as a function of time and dose, followed first-order kinetics with a half-life of 15.6 min. Absorption was not influenced by prior or concomitant administration of a variety of drugs. Absorption from other regions of the intestine was similar to that from the duodenum; in contrast, absorption from the stomach was markedly slower. Gastric absorption was increased by alkalinization of stomach contents but was still considerably slower than from the duodenum. Gastric emptying of methadone appears to be the rate-limiting step in the overall gastrointestinal absorption of the drug, since the rate of emptying following intubation of the drug into the stomach was also considerably slower than the rate of duodenal absorption.

摘要

采用体内肠段技术研究了dl-美沙酮在斯普拉格-道利大鼠胃肠道的吸收情况。以时间和剂量为函数测定的十二指肠吸收符合一级动力学,半衰期为15.6分钟。吸收不受多种药物的预先给药或同时给药的影响。肠道其他部位的吸收与十二指肠相似;相比之下,胃的吸收明显较慢。胃内容物碱化可增加胃的吸收,但仍比十二指肠吸收慢得多。美沙酮的胃排空似乎是该药物胃肠道整体吸收的限速步骤,因为将药物插管入胃后的排空速率也比十二指肠吸收速率慢得多。

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