Clinical Pharmacology of Intravenously Administered Trimethoprim-Sulfamethoxazole

Author:

Grose William E.1,Bodey Gerald P.1,Loo Ti Li1

Affiliation:

1. Department of Developmental Therapeutics, The University of Texas System Cancer Center-M. D. Anderson Hospital and Tumor Institute, Houston, Texas 77030

Abstract

Pharmacokinetic studies of intravenously administered trimethoprim-sulfamethoxazole (TMP-SMX) were conducted in 11 patients with cancer while they received therapy with this drug combination for infection. Each patient received 160 mg of TMP and 800 mg of SMX every 8 h. The highest plasma concentrations of both agents were attained at the end of a 1-h infusion period, and the levels were maintained above 38 μg of free SMX and 2 μg of TMP per ml for 2 to 4 h on day 1. On day 4, these concentrations were exceeded at all time intervals of blood sampling. High concentrations of TMP and free SMX were recovered in the urine during the 8-h period. The plasma half-lives of TMP and free SMX, as determined during the first 8-h period, were 7.6 and 8.6 h, respectively. Compared with SMX, TMP had an approximately 2.5 times higher volume of distribution. This drug combination was well tolerated by the patients and unaccompanied by drug-related toxicity.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

Reference20 articles.

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2. Absorption and urinary excretion of trimethoprim, sulfamethoxazole, and trimethoprim-sulfamethoxazole: results with single doses in normal young adults and preliminary observations during therapy with trimethoprim-sulfamethoxazole;Bach M. C.;J. Infect. Dis.,1973

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4. Bacteriological, pharmacological, and clinical studies with trimethoprim-sulfonamide combinations with particular reference to the treatment of urinary infections;Brumfitt W.;Postgrad. Med. J.,1969

5. Trimethoprim-sulfamethoxazole: in vitro microbiological aspects;Bushby S. R. M.;J. Infect. Dis.,1973

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