Pharmacological Studies with 5-Fluorocytosine

Author:

Block Edward R.1,Bennett John E.1

Affiliation:

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

Abstract

A cylinder plate bioassay for 5-fluorocytosine (5-FC) is described which permits determination of 5-FC concentrations in biological fluids in the presence of amphotericin B. Using this assay, we determined serum concentrations in 12 patients after a single dose of drug and in 8 patients receiving daily 5-FC at 6-hr intervals (4 to 120 days). Drug was detectable in serum as early as 0.5 hr and concentrations were measurable as long as 24 hr after a dose, regardless of renal function. Peak concentrations occurred 6 hr after the initial drug dose, but were seen between 1 and 2 hr after a dose in all patients receiving a minimum of 4 days of therapy. Mild to moderate renal impairment produced marked increases in peak 5-FC concentrations in the serum of a group of eight patients on three different dosage schedules. Five patients were studied before and after amphotericin B-induced renal insufficiency. Peak concentrations increased from 14 to 142% concomitant with the change in renal function. Parallel studies in rabbits confirmed the results in our patients. 5-FC half-life in the serum of 10 rabbits increased from 3.35 ± 0.27 to 24.63 ± 0.70 hr after experimentally induced acute renal failure. Concentrations of 5-FC in the cerebrospinal fluid of five patients ranged from 17 to 62 μg/ml and were 74.4 ± 5.6% of simultaneously determined serum concentrations. The effect of renal function on 5-FC concentrations in cerebrospinal fluid was similar to that seen with serum.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

Reference19 articles.

1. Acute toxicity of cephaloridine, an antibiotic derived from cephalosporin C;Atkinson R. M.;Toxicol. Appl. Pharmacol.,1966

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

3. 5-FC and urinarycandidiasis;Davies R. R.;Brit. Med. J.,1971

4. 5-FC in the treatment of cryptococcal and Candida mycosis;Fass R. J.;Ann. Intern. Med.,1971

5. Observations on the activity of two newer antifungal agents saramycetin and 5-fluorocytosine;Grunberg E.;Int. Congr. Chemother., 5th, Vienna, p.,1967

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