Yacobi A, Levy G
J Pharm Sci. 1979 Jun;68(6):742-6. doi: 10.1002/jps.2600680624.
This investigation determined the effect of serum protein binding on the kinetics of sulfisoxazole distribution, metabolism, and excretion. Adult rats, whose serum free fraction of sulfisoxazole (at a total concentration of 81 +/- 6 micrograms/ml) was 0.05-0.24, received a rapid intravenous injection of 20 mg/kg. Sulfisoxazole concentrations in plasma declined biexponentially with time. There were pronounced and reproducible interindividual differences in the total, metabolic, and renal sulfisoxazole clearances, each positively correlated with the serum free fraction of sulfisoxazole. The renal sulfisoxazole clearance had a component unaffected by serum protein binding. The apparent central compartment volume increased with an increasing serum free sulfisoxazole fraction, but the latter had not apparent effect on the first exponential term of the biexponential equation describing sulfisoxazole elimination kinetics in rats. Serum protein binding was a major determinant of intersubject differences in sulfisoxazole excretion and biotransformation kinetics.
本研究确定了血清蛋白结合对磺胺异恶唑分布、代谢和排泄动力学的影响。成年大鼠血清中磺胺异恶唑的游离分数(总浓度为81±6微克/毫升)为0.05 - 0.24,快速静脉注射20毫克/千克。血浆中磺胺异恶唑浓度随时间呈双指数下降。磺胺异恶唑的总清除率、代谢清除率和肾清除率存在明显且可重复的个体间差异,每一项均与磺胺异恶唑的血清游离分数呈正相关。肾磺胺异恶唑清除率有一个不受血清蛋白结合影响的成分。表观中央室容积随血清游离磺胺异恶唑分数的增加而增加,但后者对描述大鼠磺胺异恶唑消除动力学的双指数方程的第一个指数项没有明显影响。血清蛋白结合是磺胺异恶唑排泄和生物转化动力学个体间差异的主要决定因素。