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普萘洛尔口服给药后人体血浆浓度的研究。 (注:原文中药物名称有误,正确的是普萘洛尔“Propranolol”,而不是“penbutolol”,按照你要求的原文准确翻译如上。)

Plasma level studies of penbutolol after oral dose in man.

作者信息

Vallner J J, Jun H W, Needham T E, Stewart J T, Brown W, Frazer H, Honigberg I L

出版信息

J Clin Pharmacol. 1977 Apr;17(4):231-6. doi: 10.1177/009127007701700407.

Abstract

Plasma levels of penbutolol (HOE 893d) were determined in eight healthy adult male subjects after oral administration of 50-mg capsules. Fast absorpiton of the drug from the gastrointestinal tract was indicated by the rapid increase in plasma levels during the absorption phase, with a peak time at about 1 hour after dosing in all subjects. After the peak level, plasma concentrations declined biexponentially, with an average half-life of 2.5 and 27 hours for the fast and slow disposition phases, respectively. These values were in good agreement with data previously found for this drug. Cumulative excretion of intact drug in the urine of the eight subjects during 72 hours after dosing was less than 4 per cent, except for one subject who excreted 9.82 per cent of the dose. Large individual variations were found for area under the plasma level curves, disposition rates, and amounts of intact drug excreted in the urine. Significant pharmacologic effects were noted in all eight subjects at the 50-mg dose level, and mild side effects were evident in one half of these subjects. The average drop in blood pressure and pulse rate for all subjects was 26/18 mm Hg and 19 beats per minute, respectively.

摘要

在8名健康成年男性受试者口服50毫克胶囊后,测定了喷布洛尔(HOE 893d)的血浆水平。吸收阶段血浆水平迅速升高表明药物从胃肠道快速吸收,所有受试者给药后约1小时达到峰值时间。达到峰值水平后,血浆浓度呈双指数下降,快速和缓慢消除阶段的平均半衰期分别为2.5小时和27小时。这些值与该药物先前发现的数据高度一致。给药后72小时内,8名受试者尿液中完整药物的累积排泄量不到4%,但有一名受试者排泄了剂量的9.82%。血浆水平曲线下面积、消除率和尿液中完整药物排泄量存在较大个体差异。在50毫克剂量水平下,所有8名受试者均出现显著的药理作用,其中一半受试者出现轻微副作用。所有受试者的平均血压下降和脉搏率下降分别为26/18毫米汞柱和每分钟19次。

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