TY - JOUR T1 - Dose-Dependent Pharmacokinetics of Cyclosporin A in Rats: Events in Tissues JF - Drug Metabolism and Disposition JO - Drug Metab Dispos SP - 582 LP - 589 VL - 28 IS - 5 AU - Chiaki Tanaka AU - Ryosei Kawai AU - Malcolm Rowland Y1 - 2000/05/01 UR - http://dmd.aspetjournals.org/content/28/5/582.abstract N2 - Cyclosporin A (CyA) tissue distribution kinetics was extensively studied after single 1.2-, 6-, and 30-mg/kg CyA doses (via 2-min i.v. infusion) to rats. Drug concentrations in blood and various tissues were measured using a specific radioimmunoassay. Based on total blood concentration data alone, CyA systemic pharmacokinetics appeared essentially linear. However, after taking the saturable, nonlinear blood cell binding into account, multiple nonlinear factors were identified. Intrinsic clearance at 30 mg/kg was about half the value at the two lower doses. Tissue distribution was also dose-dependent, with evidence of saturable binding in many tissues. In general, blood binding saturation (dissociation constantKD = 0.18 μg/ml) occurred at a lower dose (concentration) than saturation of tissue binding (KD, 0.005–0.77 μg/g), such that the volume of distribution at steady state first increased as the dose increased from 1.2 to 6 mg/kg, and then decreased as the dose increased to 30 mg/kg. Tissue binding was further investigated by various graphical analyses. Some organs showed a monophasic (single site) Scatchard plot of the tissue data at steady state, with highKD values. In other organs, biphasic binding characteristics were observed with the KDvalues of the high-affinity site in the same range as theKD reported for the binding of CyA with cyclophilin, the putative target. Saturable tissue binding may therefore influence not only the pharmacokinetics but also the efficacy of CyA. The American Society for Pharmacology and Experimental Therapeutics ER -