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不同剂型丁咯地尔的药代动力学

Pharmacokinetics of buflomedil after various dosage forms.

作者信息

Zecca L, Ferrario P, Pirola R, Reina L, Zambotti F, Zonta N, Lepore A M, Scaglione F, Fraschini F

机构信息

Consiglio Nazionale delle Ricerche, Istituto di Tecnologie Biomediche Avanzate, Milan, Italy.

出版信息

Arzneimittelforschung. 1989 Apr;39(4):518-9.

PMID:2751740
Abstract

The pharmacokinetic disposition of buflomedil was compared in humans after oral administration of solution, tablets and film tablets. Six healthy male volunteers received a single oral dose of the three different dosage formulations. Blood and urine samples were taken before dosing and at selected times over 24 h and 72 h, resp., after dosing. The concentration of the drug in samples was measured by gas-chromatography with nitrogen detector. The absorption of buflomedil was faster after solution administration, while other plasma parameters did not show any major differences. Also the amount of drug excreted in urines was higher with solution dosing.

摘要

在人类口服溶液剂、片剂和薄膜衣片后,对丁咯地尔的药代动力学特征进行了比较。六名健康男性志愿者接受了三种不同剂型的单次口服剂量。给药前以及给药后分别在24小时和72小时的选定时间采集血液和尿液样本。通过带氮检测器的气相色谱法测量样本中药物的浓度。溶液剂给药后丁咯地尔的吸收更快,而其他血浆参数未显示出任何重大差异。溶液剂给药时尿液中排泄的药物量也更高。

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