呋喃妥因在怀孕大鼠体内的药代动力学。

Problemy medycyny wieku rozwojowego Pub Date : 1984-01-01
K Wierzba, B Wańkowicz, J Prokopczyk, A Piekarczyk
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引用次数: 0

摘要

研究了呋喃妥因(NTF)在妊娠大鼠体内的药代动力学,以估计其在胎儿单位的累积。结果表明,NTF在非妊娠大鼠体内的药代动力学呈剂量依赖性。10.20和40 mg/kg NTF的生物半衰期分别从0.24 h增加到0.41 h和0.72 h。怀孕大鼠的NTF消除减少。药代动力学分析显示,妊娠大鼠体内可能存在较强的NTF积累(K12/K21比值升高)。考虑到妊娠期肾功能的增加,人们可能会怀疑NTF的消除减少是由于其在改变的组织间室中的显著积累引起的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Pharmacokinetics of nitrofurantoin in the bodies of pregnant rats].

The investigation of nitrofurantoin (NTF) pharmacokinetics in pregnant rats was undertaken to estimate its cumulation in the fetus unit. It was found that pharmacokinetics of NTF is dose-dependent in non-pregnant rats. The biological half-life time increased from 0.24 to 0.41 and 0.72 h for NTF doses 10.20 and 40 mg/kg, respectively. The elimination of NTF was diminished in pregnant rats. The pharmacokinetic analysis revealed a possibility of strong NTF accumulation in the pregnant rats (increased K12/K21 ratio). Taking into account increased renal function in pregnancy, one may suspect that decreased elimination of NTF was rather caused by its significant cumulation in the changed tissue compartment.

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