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通过14CO₂呼气分析测定人体药物代谢率。

Rate of drug metabolism in man measured by 14CO2-breath analysis.

作者信息

Platzer R, Galeazzi R L, Karlaganis G, Bircher J

出版信息

Eur J Clin Pharmacol. 1978 Dec 1;14(4):293-9. doi: 10.1007/BF00560464.

Abstract

Exhalation of 14CO2 in breath has been used to assess the rate of hepatic demethylation of (14C-dimethyl)aminopyrine, but due to the complexity of aminopyrine metabolism the pharmacokinetics of the procedure are insufficiently understood. Therefore, studies were performed in five individuals after oral administration of (14C-methoxy)glycodiazine, a model substance with relatively simple kinetic properties. Plasma concentrations of the drug and urinary output of its metabolites measured by high pressure liquid chromatography were analysed by a two-compartment open model. The terminal disappearance of 14CO2 from breath was practically identical with the terminal disappearance of glycodiazine from plasma, which could be correlated with the plasma clearance of free glycodiazine. The mean transit time of 14C-atoms from plasma to breath was 3 h. These results contribute to the pharmacokinetic basis for use of 14C-demethylation breath tests. In particular, they are consistent with the hypothesis that 14CO2-breath analysis may be used to assess certain pharmacokinetic parameters of appropriately labelled test compounds. These parameters may not necessarily be a direct reflection of the rate of demethylation.

摘要

呼出气体中的14CO2已被用于评估(14C-二甲基)氨基比林的肝脏去甲基化速率,但由于氨基比林代谢的复杂性,该过程的药代动力学尚未得到充分理解。因此,对五名个体口服(14C-甲氧基)格列本脲后进行了研究,这是一种具有相对简单动力学特性的模型物质。通过两室开放模型分析了通过高压液相色谱法测量的药物血浆浓度及其代谢产物的尿量。呼出气体中14CO2的终末消失与血浆中格列本脲的终末消失几乎相同,这与游离格列本脲的血浆清除率相关。14C原子从血浆到呼出气体的平均转运时间为3小时。这些结果为14C-去甲基化呼气试验的使用提供了药代动力学基础。特别是,它们与以下假设一致,即14CO2呼气分析可用于评估适当标记的测试化合物的某些药代动力学参数。这些参数不一定直接反映去甲基化速率。

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