Chang S L, Emmick K, Wedlund P J
J Pharm Sci. 1986 May;75(5):456-8. doi: 10.1002/jps.2600750507.
A new microsampling technique is described and applied to the collection of a large number of blood samples from individual rats receiving a chronic intravenous antipyrine infusion. From these samples, a detailed description of the time-course of antipyrine autoinduction of clearance in the rat was provided. Antipyrine clearance was increased 4-5-fold over 8 d of antipyrine administration, with the increase in clearance following a monoexponential process in all animals. The assumption that the time-course of induction should reflect the degradation rate of induced enzymes was examined by comparing the half-life of antipyrine autoinduction with in vitro estimates for the half-life of induced cytochrome P-450 enzymes. The results of this comparison are discussed with respect to utilizing this kinetic model to quantitate the turnover of drug metabolism enzymes in vivo.
描述了一种新的微量采样技术,并将其应用于从接受慢性静脉注射安替比林的个体大鼠中采集大量血样。从这些样本中,详细描述了大鼠体内安替比林清除率的自身诱导随时间变化的过程。在给予安替比林的8天内,安替比林清除率增加了4至5倍,所有动物的清除率增加均遵循单指数过程。通过比较安替比林自身诱导的半衰期与体外诱导细胞色素P-450酶半衰期的估计值,检验了诱导过程的时间进程应反映诱导酶降解速率这一假设。针对利用该动力学模型定量体内药物代谢酶的周转情况,讨论了该比较结果。