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静脉注射阿托品在正常人体受试者中的血浆药代动力学。

Plasma pharmacokinetics of intravenously administered atropine in normal human subjects.

作者信息

Adams R G, Verma P, Jackson A J, Miller R L

出版信息

J Clin Pharmacol. 1982 Oct;22(10):477-81. doi: 10.1002/j.1552-4604.1982.tb02638.x.

Abstract

The pharmacokinetics of atropine (dl-hyoscyamine) was studied in six normal volunteers following a single 1-mg intravenous dose of atropine. Atropine plasma levels were collected for 24 hours and analyzed by radioimmunoassay. Pulse rates were monitored and compared with predose values in each subject. Atropine plasma concentrations were fitted by least-squares regression analysis. The observed maximal increase in pulse rate, at 12 to 16 minutes after the dose, correlated with the maximum predicted tissue levels of atropine based on the computer fit of the plasma atropine concentration-time data. No correlation between the time of maximum response and atropine plasma concentrations was observed. The average half-life of atropine was 4.125 hours. This data may be used to design a multiple-dosing regimen for intravenous atropine in patients.

摘要

对6名正常志愿者单次静脉注射1毫克阿托品(消旋莨菪碱)后,研究了阿托品的药代动力学。收集24小时的阿托品血浆水平,并通过放射免疫分析法进行分析。监测脉搏率并与每个受试者的给药前值进行比较。通过最小二乘法回归分析拟合阿托品血浆浓度。观察到给药后12至16分钟脉搏率的最大增加,与基于血浆阿托品浓度-时间数据的计算机拟合预测的阿托品最大组织水平相关。未观察到最大反应时间与阿托品血浆浓度之间的相关性。阿托品的平均半衰期为4.125小时。该数据可用于设计患者静脉注射阿托品的多剂量给药方案。

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