马越鸣, 孙瑞元. 安定在家兔体内的肠胃循环药代动力学分析J. 药学学报, 1993, 28(9): 651-654.
引用本文: 马越鸣, 孙瑞元. 安定在家兔体内的肠胃循环药代动力学分析J. 药学学报, 1993, 28(9): 651-654.
YM Ma, RY Sun. PHARMACOKINETIC ANALYSIS OF ENTEROGASTRIC CIRCULATION OF DIAZEPAM IN RABBITSJ. Acta Pharmaceutica Sinica, 1993, 28(9): 651-654.
Citation: YM Ma, RY Sun. PHARMACOKINETIC ANALYSIS OF ENTEROGASTRIC CIRCULATION OF DIAZEPAM IN RABBITSJ. Acta Pharmaceutica Sinica, 1993, 28(9): 651-654.

安定在家兔体内的肠胃循环药代动力学分析

PHARMACOKINETIC ANALYSIS OF ENTEROGASTRIC CIRCULATION OF DIAZEPAM IN RABBITS

  • 摘要: 6只家兔iv安定5 mg·kg-1后,浓度—时间数据呈现双峰形。本文提出肠胃循环动力学模型,用于分析实测数据,得到了一般动力学参数:T1/2(α)=0.21±=0.15 h,T1/2(β)=2.2+0.6 h,Ke=1.5±0.6 h-1,K12=2.0±1.0 h-1,K21=1.0±0.4 h-1,V1=3.1±1.6 L·kg-1,AUC=1.7±0.5μg·h-1·ml-1。此外,还求得有关肠胃循环的参数,即:重吸收滞后时间T′=0.25±0.24h,重吸收速率常数KA=3.5±1.4 h-1,重吸收率RA=24±7%。

     

    Abstract: The concentration-time curves of diazepam exhibited double peaks after iv 5 mg·kg-1 to 6 rabbits. A pharmacokinetic model taking account of enterogastric circulation was proposed to explain this double-peak phenomenon and showed good agreement with data. This model pro-vides not only the ordinary pharmacokinetic parameters: T1/2(α)=0.21±0.15 h, T1/2(β)=2.2±0.6 h, Ke=1.5±0.6 h-1, K12=2.0±1.0 h-1, K21=1.0±0.4 h-1, V1=3.1±1.6 L·kg-1, AUC=1.7±0.5 μg·h-1·ml-1, but also the parameters of enterogastric circulation of diazepam: lag time of reabsorption T'=0.25±0.24 h, reabsorption rate constant Ka=3.5±1.4 h-1, reabsorption rate Ra=24±7%.

     

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