PT - JOURNAL ARTICLE AU - J Ishizaki AU - E Nakashima AU - K Yokogawa AU - T Nagano AU - T Takayasu AU - F Ichimura TI - A physiologically based pharmacokinetic model for (-)-quinuclidinyl benzylate using nonlinear irreversible tissue binding parameters in rats. DP - 1992 Jul 01 TA - Drug Metabolism and Disposition PG - 485--489 VI - 20 IP - 4 4099 - http://dmd.aspetjournals.org/content/20/4/485.short 4100 - http://dmd.aspetjournals.org/content/20/4/485.full SO - Drug Metab Dispos1992 Jul 01; 20 AB - The disposition characteristics of (-)-quinuclidinyl benzylate (QNB) were investigated in rats, and a physiologically based pharmacokinetic model was established using its linear and nonlinear tissue binding parameters. The steady-state distribution volume (Vdss) and systemic clearance (CLtot) were comparable after iv administration of 325 ng/kg and 3.2 mg/kg, suggesting that QNB pharmacokinetics based on plasma concentrations is linear. However, tissue accumulation was observed in the heart, lung, muscle, and brain. This accumulation persisted for over 12 hr after the iv administration of 325 ng/kg [3H]QNB. Tissue binding parameters were determined after continuous infusion of QNB. Irreversible and nonlinear binding parameters were obtained in various regions of the brain and other tissues. Reversible equilibrium concentration ratios between tissue and plasma were determined after high-dose infusion. QNB concentrations in the plasma, heart, lung, muscle, and brain were predicted after the administration of 325 ng/kg or 3.2 mg/kg. There was reasonable agreement between the model predictions and the observed data.