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托拉洛尔治疗高血压的药代动力学

Pharmacokinetics of tolamolol in the treatment of hypertension.

作者信息

Routledge P A, Davies D M, Rawlins M D

出版信息

Eur J Clin Pharmacol. 1977 Nov 14;12(3):171-4. doi: 10.1007/BF00609855.

Abstract

Tolamolol was administered in a "double-blind" study to fifteen hypertensive patients by dose-titration against arterial blood pressure. Mean steady-state plasma tolamolol concentrations (Css) were determined for each patient from the area under the plasma concentration--time curve during a dosage interval whilst patients were receiving optimal tolamolol doses. No significant correlation was observed between daily tolamolol dose and Css; the relationship between fall in lying mean arterial pressure and Css also failed to reach conventional levels of statistical significance, but Css was observed to be correlated with the fall in standing pressure. The results suggest that plasma concentrations in excess of 200 ng/ml may be required to achieve an effective hypothensive response with the drug.

摘要

在一项“双盲”研究中,通过根据动脉血压进行剂量滴定,给15名高血压患者服用了托拉洛尔。在患者接受最佳托拉洛尔剂量期间,根据给药间隔期血浆浓度-时间曲线下的面积,为每位患者测定了平均稳态血浆托拉洛尔浓度(Css)。未观察到每日托拉洛尔剂量与Css之间存在显著相关性;卧位平均动脉压下降与Css之间的关系也未达到传统的统计学显著水平,但观察到Css与立位血压下降相关。结果表明,可能需要超过200 ng/ml的血浆浓度才能通过该药物实现有效的降压反应。

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