Intravenous cyclosporine kinetics in renal failure

Ferenc Follath*, Markus Wank, Samuel Vozeh, Gilbert Thiel, Felix Brunner, Rolf Loertscher, Michel Lemaire, Kurt Nussbaumer, Werner Niederberger, Alan Wood

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

90 Citations (Scopus)

Abstract

Kinetics of the novel immunosuppressive cyclosporine were determined in four patients with terminal renal failure. After a short intravenous infusion (2.05 to 3.5 mg/kg in 4 hr), blood and plasma concentrations were measured (HPLC and radioimmunoassay [RIA]) up to 36 hr. After infusion, concentration curves of the drug were characterized by a rapid initial fall (t 1 2α 0.10 ± 0.03 hr), followed by a biphasic elimination phase with corresponding t 1 2S of 1.08 ± 0.25 hr (t 1 2β) and 15.8 ± 8.4 hr (t 1 2γ). The volumes of distribution, calculated from whole blood concentrations (HPLC), were 0.140 ± 0.48 l/kg (volume of the central compartment) and 3.49 ± 2.65 l/kg (volume of distribution at steady state), whereas systemic clearances were 0.369 ± 0.08 l/hr/kg. Blood levels measured by RIA exceeded the HPLC values after the fourth hour by up to 100%, indicating the production of cross-reacting cyclosporine metabolites. Plasma concentrations were considerably lower than in whole blood. Elimination of unchanged cyclosporine in patients with renal failure appears to be of the same order as in those with normal kidney function. Modification of the initial dosage regimens is therefore probably not required.

Original languageEnglish
Pages (from-to)638-643
Number of pages6
JournalClinical Pharmacology and Therapeutics
Volume34
Issue number5
DOIs
Publication statusPublished - Nov 1983
Externally publishedYes

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