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新生儿氨苄西林血清浓度的药代动力学模型。

Pharmacokinetic model for serum concentrations of ampicillin in the newborn infant.

作者信息

Colburn W A, Gilbaldi M, Yoshioka H, Takimoto M, Riley H D

出版信息

J Infect Dis. 1976 Jul;134(1):67-9. doi: 10.1093/infdis/134.1.67.

Abstract

The time course of ampicillin concentrations in the sera of three newborn infants during and upon termination of intravenous infusion at a constant rate can be described by a two-compartment pharmacokinetic model. The parameters of the model were determined by simultaneously fitting the serum concentration data obtained during and after the infusion by means of a nonlinear regression program with the aid of a digital computer. The half-life of ampicillin in the infants ranged from 2.1 to 2.9 hr; these values are more than twice those observed in adults with normal renal function.

摘要

以恒定速率静脉输注期间及结束时,三名新生儿血清中氨苄西林浓度的时程可用二室药代动力学模型来描述。借助数字计算机,通过非线性回归程序对输注期间及之后获得的血清浓度数据进行同时拟合,从而确定该模型的参数。婴儿体内氨苄西林的半衰期为2.1至2.9小时;这些数值是肾功能正常的成年人中所观察到数值的两倍多。

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