Bevill R F, Koritz G D, Dittert L W, Bourne D W
J Pharm Sci. 1977 Sep;66(9):1297-300. doi: 10.1002/jps.2600660923.
The plasma, urine, and tissue sulfathiazole concentrations were determined at various times following intravenous administration to 12 sheep. The plasma and urine data were consistent with a one-compartment pharmacokinetic model, with an elimination half-life of 1.1 hr and a volume of distribution of 0.39 liter/kg. Sulfathiazole was eliminated by excretion of unchanged drug in urine (67%) and by formation of two metabolites. The data obtained from eight tissue sites were consistent with the one-compartment pharmacokinetic model presented and confirmed that tissue residues of sulfathiazole can be calculated from serum and urine drug concentration.
给12只绵羊静脉注射后,在不同时间测定了血浆、尿液和组织中的磺胺噻唑浓度。血浆和尿液数据符合单室药代动力学模型,消除半衰期为1.1小时,分布容积为0.39升/千克。磺胺噻唑通过尿液中未变化药物的排泄(67%)和两种代谢物的形成而消除。从八个组织部位获得的数据与所提出的单室药代动力学模型一致,并证实可以根据血清和尿液药物浓度计算磺胺噻唑的组织残留量。