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东莨菪碱在剖宫产患者中的药代动力学及临床效应

Pharmacokinetics and clinical effects of scopolamine in caesarean section patients.

作者信息

Pihlajamäki K K, Kanto J H, Oksman-Caldentey K M

出版信息

Acta Pharmacol Toxicol (Copenh). 1986 Oct;59(4):259-62. doi: 10.1111/j.1600-0773.1986.tb00166.x.

Abstract

A new method (ELISA) was used to evaluate the pharmacokinetics of scopolamine following intravenous (0.005 mg/kg), intramuscular (0.01 mg/kg), and oropharyngeal (0.035 mg/kg) administration of the drug to pregnant patients anaesthetized for caesarean section. After intravenous (N = 4) the drug fast disappeared from the circulation with a half-life of about 5 min., and the serum levels generally were measurable up to 3 hours, mean elimination half-life was 1.85 hours. A fast absorption was found after intramuscular injection, tmax = 10 min. (N = 4), and the drug had a clinically significant oropharyngeal absorption as well, tmax was around 1 hour (N = 6). The intramuscular and oropharyngeal, but not the intravenous, administrations produced a marked postoperative sedative and amnesic effects. All three administration ways caused a significant antisecretory action.

摘要

采用一种新方法(酶联免疫吸附测定法,ELISA),对剖宫产麻醉的孕妇静脉注射(0.005mg/kg)、肌肉注射(0.01mg/kg)和口咽给药(0.035mg/kg)东莨菪碱后的药代动力学进行评估。静脉注射后(n = 4),药物迅速从循环中消失,半衰期约为5分钟,血清水平通常在3小时内可测,平均消除半衰期为1.85小时。肌肉注射后吸收迅速,达峰时间为10分钟(n = 4),该药物口咽给药也有显著吸收,达峰时间约为1小时(n = 6)。肌肉注射和口咽给药,而非静脉注射,产生显著的术后镇静和遗忘作用。三种给药方式均引起显著的抗分泌作用。

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