The tissue penetration, as measured by a blister technique, and pharmacokinetics of cefsulodin compared with carbenicillin and ticarcillin
C. D. Findlay, Robert A. Wise, J. E. Allcock, S.R. Durham
Abstract
C. D. Findlay, Robert A. Wise, J. E. Allcock, S.R. Durham
Abstract
Serum and cantharides-induced blister fluid levels of cefsulodin, carbenicillin and ticarcillin were compared in a semi-crossover study, after a I g intravenous bol us injection. The serum concentration/time curves for the three β-lactams were essentially similar, the half-lives being 1·25–1·5 h. Cefsulodin and ticarcillin penetrated into the fluid to a greater extent than carbenicillin. As cefsulodin is a more potent antibiotic against Pseudomonas aeruginosa it is suggested that this may be the agent of choice in treating infections caused by this pathogen.
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Serum and cantharides-induced blister fluid levels of cefsulodin, carbenicillin and ticarcillin were compared in a semi-crossover study, after a I g intravenous bol us injection. The serum concentration/time curves for the three β-lactams were essentially similar, the half-lives being 1·25–1·5 h. Cefsulodin and ticarcillin penetrated into the fluid to a greater extent than carbenicillin. As cefsulodin is a more potent antibiotic against Pseudomonas aeruginosa it is suggested that this may be the agent of choice in treating infections caused by this pathogen.
Key concepts: Cefsulodin, Ticarcillin, Carbenicillin, Pharmacokinetics, Antibiotics, Pseudomonas aeruginosa, Microbiology, Medicine