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Antimicrobial Agents and Chemotherapy, October 1999, p. 2451-2456, Vol. 43, No. 10
Department of Medicine, Albany Medical
College, Albany, New York,1 and
Schering-Plough Research Institute, Kenilworth, New
Jersey2
Received 17 November 1998/Returned for modification 17 April
1999/Accepted 20 July 1999
Ribavirin has recently been demonstrated to have efficacy in
combination with alpha interferon for treatment of relapsed hepatitis C. The marked improvement in the response rate after treatment with the
combination regimen (10-fold higher versus that from monotherapy with
alpha interferon) highlights the importance of determining the absolute
bioavailability of ribavirin as a first step in beginning to
investigate the pharmacodynamics of the combination. The objective of
this study was to determine the absolute bioavailability of ribavirin
with an intravenous formulation containing ribavirin labeled with the
stable isotope 13C3
(13C3-ribavirin) and unlabeled oral ribavirin.
Six healthy volunteers received 150 mg of intravenous
13C3-ribavirin followed 1 h later by a
400-mg oral dose of ribavirin. Samples of blood and urine were
collected up to 169 h postdosing. Concentrations of
13C3-ribavirin and unlabeled ribavirin were
determined by a high-performance liquid chromatography tandem mass
spectrometric method. All plasma and urine data were comodeled for
labeled and unlabeled ribavirin by using both the two- and
three-compartment models in the program ADAPT II. A three-compartment
model was chosen for the pharmacokinetic analysis with the Akaike
Information Criterion. The mean maximum concentrations of drug in
plasma for intravenous and oral ribavirin were 4,187 and 638 ng/ml,
respectively. The mean bioavailability was 51.8% ± 21.8%, and the
mean
0066-4804/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Pharmacokinetics and Absolute Bioavailability of
Ribavirin in Healthy Volunteers as Determined by
Stable-Isotope Methodology
-phase half-life was 37.0 ± 14.2 h. The mean renal
clearance, metabolic clearance, and volume of distribution of the
central compartment were 6.94 liters/h, 18.1 liters/h, and 17.8 liters,
respectively. The use of the stable-isotope methodology has provided
the best estimate of the absolute bioavailability of ribavirin that is
currently available, as there was neither a period bias nor a washout
effect to confound the data. The study demonstrated that the mean
bioavailability for a 400-mg dose of ribavirin was 52%, which is
higher than that previously reported in other investigations.
*
Corresponding author. Mailing address: Department of
Medicine A-142, Albany Medical College, 47 New Scotland Ave., Albany, NY 12208. Phone: (518) 262-6970. Fax: (518) 262-6333. E-mail: sandra_preston{at}ccgateway.amc.edu.
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