1 In vivo microdialysis with HPLC was used to investigate the pharmacokinetics of pe¯oxacin and its interaction with cyclosporin A. Microdialysis probes were inserted into the jugular vein/right atrium, the striatum and the bile duct of male Sprague-Dawley rats. Biological¯uid sampling thereby allowed the simultaneous determination of pe¯oxacin levels in blood, brain and bile. 2 Following pe¯oxacin administration, the brain-to-blood coecient of distribution was 0.036. This was calculated by dividing the area under the concentration curve (AUC) of pe¯oxacin in brain by its AUC in blood (k=AUC brain /AUC blood ). 3 When the P-glycoprotein cyclosporin A (10 mg kg
71) was co-administered with pe¯oxacin (10 mg kg 71 ), the AUC and the mean residence time in rat blood did not dier signi®cantly (P40.05). Similarly, the pharmacokinetics of pe¯oxacin in rat brain was not aected by the presence of cyclosporin A. 4 The AUC of unbound pe¯oxacin in bile was signi®cantly greater than that in blood. The disposition of pe¯oxacin in rat bile shows a slow elimination phase following a peak concentration 30 min after pe¯oxacin administration (10 mg kg 71 , i.v.). The bile-to-blood coecient of distribution (k=AUC bile /AUC blood ) was 1.53. 5 The results indicated that pe¯oxacin was able to penetrate the blood-brain barrier and that the concentration in bile was greater than that in the blood, suggesting active biliary excretion of pe¯oxacin. Current data obtained from rats show no signi®cant impact of cyclosporin A on the pharmacokinetics of pe¯oxacin in rat blood and brain when administered by concomitant i.v. bolus.