硝基喹啉的临床药代动力学。

A Mrhar, Z Kopitar, F Kozjek, V Presl, R Karba
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引用次数: 0

摘要

大鼠口服14c -硝基喹啉,分别用放射自显影法和放射性测量法测定其分布及血浆和胆汁水平。同时,对人体志愿者口服和静脉注射三种不同剂量的硝基喹啉,用分光光度法测定非共轭和共轭硝基喹啉的尿浓度。在此基础上建立药代动力学模型。在模拟-混合计算机上模拟的尿中硝基喹啉总累积量与模型响应之间的曲线拟合过程可以评估所选模型的有效性以及模型参数的识别。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinical pharmacokinetics of nitroxoline.

14C-Nitroxoline was given orally to the rats, and its distribution as well as plasma and bile levels were determined autoradiographically and by the aid of radioactivity measurements, respectively. Nitroxoline was also given to the human volunteers orally and intravenously in three various doses and the corresponding urine concentrations of unconjugated and conjugated nitroxoline were determined spectrophotometrically. A pharmacokinetical model was generated on the basis of the results. The curve fitting procedure between total nitroxoline cumulative quantities in urine and the model response simulated on analog-hybrid computer enabled the evaluation of the validity of the chosen model as well as of the identification of its parameters.

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