头孢菌素
头孢哌酮
药代动力学
头孢呋辛
头孢菌素
化学
塞切姆
药理学
分配量
分布(数学)
抗菌剂
医学
抗生素
生物化学
数学
数学分析
抗生素耐药性
羧酸
亚胺培南
作者
Mario Eandi,I Viano,M Santiano
出处
期刊:PubMed
日期:1982-01-01
卷期号:4 (3): 179-84
被引量:1
摘要
We made a pharmacokinetic study of the cephalosporins cephazolin, cephaloridine, cefoperazone, and cefuroxime in the rabbit. We computed the pharmacokinetic parameters of a two-compartment open model from the plasma concentration time curves obtained at different increasing doses. Cephazolin, cephaloridine and cefoperazone demonstrated a dose dependent kinetics since the constants of apparent rate of elimination and apparent volume of distribution varied with the doses. In order to evaluate the extra-renal of elimination, we performed pharmacokinetic analysis on the same animals after nephrectomy. While cephazolin, cephaloridine and cefuroxime were eliminated primarily through the kidneys, cefoperazone was largely eliminated by extrarenal pathways.
科研通智能强力驱动
Strongly Powered by AbleSci AI