Watari N, Aizawa K, Kaneniwa N
J Pharm Sci. 1985 Feb;74(2):165-70. doi: 10.1002/jps.2600740212.
A pharmacokinetic study on the renal excretion of nitrofurantoin was carried out in rabbits at doses ranging from 0.5 to 15 mg/kg. With increasing dose, nonlinear kinetics were observed in the tubular secretion, which appeared to show dose and time dependence. The disposition of nitrofurantoin after intravenous injection is well described by a one-compartment model with simultaneous first-order nonrenal elimination and renal elimination, which consists of glomerular filtration, active tubular secretion conforming to the Michaelis-Menten equation, and reabsorption clearance by nonionic diffusion. Plasma and urinary excretion data after intravenous injection of nitrofurantoin were fitted to this model. When the Michaelis constant was loosely restricted at a constant value, the maximum velocity decreased with increasing dose of nitrofurantoin. However, the Michaelis constant apparently increased with increasing dose when the maximum velocity was loosely restricted at a constant value. Although the results of this fitting suggested that the former case may occur in the active tubular secretory system, the latter case could not be completely eliminated because of limited data. The implications of these results are discussed on the basis of the available published data.
在兔子身上进行了一项关于呋喃妥因经肾排泄的药代动力学研究,剂量范围为0.5至15mg/kg。随着剂量增加,在肾小管分泌中观察到非线性动力学,其似乎呈现剂量和时间依赖性。静脉注射后呋喃妥因的处置情况可用一个一室模型很好地描述,该模型同时存在一级非肾消除和肾消除,肾消除包括肾小球滤过、符合米氏方程的主动肾小管分泌以及通过非离子扩散的重吸收清除。将静脉注射呋喃妥因后的血浆和尿排泄数据拟合到该模型。当米氏常数大致限定为一个恒定值时,最大速度随呋喃妥因剂量增加而降低。然而,当最大速度大致限定为一个恒定值时,米氏常数显然随剂量增加而增大。尽管这种拟合结果表明前一种情况可能发生在主动肾小管分泌系统中,但由于数据有限,后一种情况也不能完全排除。根据已发表的现有数据对这些结果的意义进行了讨论。