Amphotericin B Pharmacokinetics in Humans

Author:

Atkinson Arthur J.1,Bennett John E.2

Affiliation:

1. Clinical Pharmacology Center, Departments of Medicine and Pharmacology, Northwestern University Medical School, Chicago, Illinois 60611,

2. Clinical Myocology Section, Laboratory of Clinical Investigation, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland 20014

Abstract

The pharmacokinetics of amphotericin B were studied in two patients at the conclusion of long-term therapy for disseminated histoplasmosis. The distribution kinetics of this drug were adequately described by a three-compartment mamillary model with a total distribution volume averaging 4 liters/kg. The elimination phase half-life of amphotericin B was approximately 15 days, reflecting slow release of amphotericin B from a peripheral compartment. In accordance with previous reports, renal excretion accounted for only 3% of total amphotericin B elimination. The pharmacokinetic model for one of the patients also was used to compare the simulated amphotericin B serum levels that would be expected if initial therapy followed two recommended regimens.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

Reference17 articles.

1. Pharmacokinetics of intrathecally administered amphotericin B;Atkinson A. J.;Am. Rev. Resp. Dis.,1969

2. Bennett J. D. 1976. Amphotericin B binding to serum betalipoprotein p. 107-109 In K. Iwata (ed.) Recent advances in medical and veterinary mycology. University of Tokyo Press Tokyo.

3. Chemotherapy of systemic mycoses;Bennett J. E.;N. Engl. J. Med.,1974

4. Berman M. and M. F. Weiss. 1967. SAAM manual. U. S. Government Printing Office Washington D.C.

5. A pharmacologic guide to the clinical use of amphotericin B;Bindschadler D. D.;J. Infect. Dis.,1969

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