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新型口服血栓素合成酶抑制剂FCE 22,178的浓度依赖性蛋白结合

Concentration-dependent protein binding of a novel oral thromboxane synthase inhibitor--FCE 22,178.

作者信息

Li R C, Rossi D T, Narang P K

机构信息

Department of Pharmacokinetics/Dynamics Medical Research Center, Adria Laboratories, Columbus, OH 43216-6529.

出版信息

J Clin Pharmacol. 1993 Oct;33(10):933-5. doi: 10.1002/j.1552-4604.1993.tb01925.x.

Abstract

The protein binding of FCE 22,178 in humans was determined ex vivo by equilibrium dialysis using plasma samples obtained from a dose-ranging study in normal male volunteers. These data suggested that FCE 22,178 may exhibit concentration-dependent protein binding over an in vivo concentration range of .8 to 64 micrograms/mL. Increase in free fraction at higher plasma drug concentrations corresponded directly to the dose-dependent increase in renal drug clearance. Nonlinear parameter estimation showed that FCE 22,178 binds tightly to plasma proteins with an apparent equilibrium association constant of 1.44 x 10(5) mol/L. Predicted change in the free fraction is consistent with the observed changes in renal clearance.

摘要

采用从正常男性志愿者的剂量范围研究中获取的血浆样本,通过平衡透析法在体外测定了FCE 22,178在人体中的蛋白结合情况。这些数据表明,在体内浓度范围为0.8至64微克/毫升时,FCE 22,178可能表现出浓度依赖性蛋白结合。在较高血浆药物浓度下,游离分数的增加与肾药物清除率的剂量依赖性增加直接相关。非线性参数估计表明,FCE 22,178与血浆蛋白紧密结合,表观平衡缔合常数为1.44×10⁵摩尔/升。游离分数的预测变化与肾清除率的观察变化一致。

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