Pawlowska I, Pniewski T
Arzneimittelforschung. 1979;29(12):1906-11.
Two-stage pharmacokinetic studies were conducted in patients suffering from pulmonary tuberculosis treated with rifampicin (RMP). At the first stage of the studies in 100 patients blood and urinary drug levels were determined. The results showed that RMP applied orally penetrates rapidly into the circulation and reaches high serum concentrations varying largely in individual patients. At the second stage of the studies in further 30 patients blood, urinary and sputum RMP levels were simultaneously determined and the biological half-life of RMP and its distribution were checked. It was found that the biological half-life of RMP was 3.79 h, the distribution at the initial stage 38%, and after a few weeks of treatment 52.1%. The authors are of the opinion that the increased value of this parameter has a direct effect on the fall in serum RMP concentration at the later period of treatment. The amount of active RMP excreted by the kidneys of patients with lung tuberculosis averages 33.5%.
对接受利福平(RMP)治疗的肺结核患者进行了两阶段药代动力学研究。在研究的第一阶段,对100名患者测定了血液和尿液中的药物水平。结果表明,口服RMP可迅速进入循环并达到较高的血清浓度,个体患者之间差异很大。在研究的第二阶段,对另外30名患者同时测定了血液、尿液和痰液中的RMP水平,并检查了RMP的生物半衰期及其分布。结果发现,RMP的生物半衰期为3.79小时,初始阶段分布率为38%,治疗几周后为52.1%。作者认为,该参数值的增加对治疗后期血清RMP浓度的下降有直接影响。肺结核患者肾脏排泄的活性RMP量平均为33.5%。