Intravenous verapamil kinetics in rats: Marked arteriovenous concentration difference and comparison with humans

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Abstract
The pharmacokinetics of verapamil, a calcium channel blocker, were studied in male Sprague—Dawley rats following i.v. administration at a dose of 1 mg kg−1. Both arterial and venous blood were collected and the plasma drug concentrations were determined by reversed‐phase high‐performance liquid chromatography. Verapamil was distributed to the extravascular tissues very rapidly as indicated by the large Vdss (2.99±0.57 1 kg−1) and Vdβ (5.08 ± 0.541 kg−1). The apparent terminal plasma T1/2, MRTiv, and CLp were 1.59 ± 0.46, 1.26 ± 0.12 h, and 40.4 ± 9.73 ml min−1 kg−1, respectively. Marked arterial/venous differences were found with a considerable influence on the MRT and Vdss, and the terminal phase venous levels were higher than arterial levels by 103, 69, and 90%, respectively, for the three rats studied. The distribution of verapamil between plasma and erythrocytes occurred very rapidly and was identical in vitro and in vivo. The average blood to plasma and plasma to blood cell concentration ratios were 0.85 and 1.47, respectively. In contrast to propranolol, blood data rather than plasma data should be used to predict the hepatic extraction ratio of verapamil (0.87). The plasma protein binding of verapamil in humans (90%) and rats (95%) were quite similar and constant over the wide concentration range studied. A comparison of some pharmacokinetic parameters between rats and humans is presented and the potential shortcomings of using T1/2 or CLp and the advantage of using CLu (unbound plasma clearance) in interspecies scaling is also discussed.