刘晓东, 谢林, 王进, 周云曙, 王真, 刘国卿. 双部位吸收模型拟合吉非贝齐在人体中药代动力学数据J. 药学学报, 1996, 31(10): 737-741.
引用本文: 刘晓东, 谢林, 王进, 周云曙, 王真, 刘国卿. 双部位吸收模型拟合吉非贝齐在人体中药代动力学数据J. 药学学报, 1996, 31(10): 737-741.
XD Liu, L Xie, J Wang, YS Zhou, Z Wang , GQ Liu, . TWO-SITE ABSORPTION MODEL FITS FO PHARMACOKINETIC DATA OF GEMFIBROZIL IN MANJ. Acta Pharmaceutica Sinica, 1996, 31(10): 737-741.
Citation: XD Liu, L Xie, J Wang, YS Zhou, Z Wang , GQ Liu, . TWO-SITE ABSORPTION MODEL FITS FO PHARMACOKINETIC DATA OF GEMFIBROZIL IN MANJ. Acta Pharmaceutica Sinica, 1996, 31(10): 737-741.

双部位吸收模型拟合吉非贝齐在人体中药代动力学数据

TWO-SITE ABSORPTION MODEL FITS FO PHARMACOKINETIC DATA OF GEMFIBROZIL IN MAN

  • 摘要: 测定了8名受试者po吉非贝齐(Gem)600mg后血药浓度一时间数据,观察到血药浓度双峰现象。建立一种双部位吸收药动学模型拟合这些数据,实验值与拟合值吻合好,r2均大于0.99。相应参数如下:Tmax1.10±0.46h;Tmax32.60±0.73h;Cmax113.62±4.3μg·ml-1);Cmax217.22±3.83μg·ml-1);T10.06±0.06h;T21.42±0.57h;T31.79±0.60h。

     

    Abstract: The plasma concentration-time data of gemfibrozil in 8 male subjects weredetermined after an oral dose of 600 mg.Two-peak concentrations in plasma were observed.A kind ofone-compartment model with two-sites of drug absorption was proposed and used to fit these data。Agood agreement between observed and predicted data was found in all subjects with correlation indexes(γ2)>0.99.The corresponding pharmacokinetic parameters were estimated as follows:Tmax1,1.10±0.46h;Tmax2,2.60±0.73h;Cmax1,13.62±4.30μg·ml-1;Cmax2,17.22±3.83μg·ml-1;T1,0.06±0.06h;T2,1.42±0.57h and T3,1.79±0.60 h.

     

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