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Microbiology

Differences between Two New Quinolones (Gemifloxacin and Trovafloxacin) and Ciprofloxacin in Their Concentration-Dependent Killing of Streptococcus pneumoniae

Joyanes P.a · Pascual A.a · Giménez M.J.b · García I.a · Aguilar L.b · Perea E.a

Author affiliations

aMicrobiology Department, School of Medicine, University of Seville, bMedical Department, SmithKline Beecham Pharmaceuticals (GlaxoSmithKline), Madrid, Spain

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Chemotherapy 2001;47:409–414

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Article / Publication Details

First-Page Preview
Abstract of Microbiology

Published online: January 11, 2002
Issue release date: December 2001

Number of Print Pages: 6
Number of Figures: 0
Number of Tables: 2

ISSN: 0009-3157 (Print)
eISSN: 1421-9794 (Online)

For additional information: http://www.karger.com/CHE

Abstract

Background: Ciprofloxacin resistance influences the in vitro effect of new quinolones on Streptococcus pneumoniae.Methods: The early (over 3 h) in vitro bactericidal activity of gemifloxacin, trovafloxacin and ciprofloxacin was explored by time-kill tests against two ciprofloxacin-susceptible (MIC = 0.5 and 1 µg/ml) and two ciprofloxacin-resistant (MIC = 16 µg/ml) S. pneumoniae strains. Results: At subinhibitory concentrations (0.5 × MIC) and inhibitory concentrations (1 × MIC), only gemifloxacin exhibited significant bactericidal activity with, respectively, approximately 85 and approximately 95% decrease in the initial inoculum of the two ciprofloxacin-resistant strains. At concentrations similar to peak serum concentrations (1.5, 3 and 2.5 µg/ml for gemifloxacin, trovafloxacin and ciprofloxacin, respectively) after standard doses, only gemifloxacin exhibited an approximately 99.9% (3 log10) reduction in the initial inoculum for the four strains tested, regardless of their susceptibility to ciprofloxacin. No bactericidal activity was exhibited for the other two quinolones against the ciprofloxacin-resistant strains. Conclusions: Gemifloxacin offers high early bactericidal activity at concentrations similar to peak and trough levels, theoretically preventing regrowth over the dosing interval, and thus dealing with the problem of ciprofloxacin resistance in S. pneumoniae.

© 2001 S. Karger AG, Basel


Article / Publication Details

First-Page Preview
Abstract of Microbiology

Published online: January 11, 2002
Issue release date: December 2001

Number of Print Pages: 6
Number of Figures: 0
Number of Tables: 2

ISSN: 0009-3157 (Print)
eISSN: 1421-9794 (Online)

For additional information: http://www.karger.com/CHE


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Drug Dosage: The authors and the publisher have exerted every effort to ensure that drug selection and dosage set forth in this text are in accord with current recommendations and practice at the time of publication. However, in view of ongoing research, changes in government regulations, and the constant flow of information relating to drug therapy and drug reactions, the reader is urged to check the package insert for each drug for any changes in indications and dosage and for added warnings and precautions. This is particularly important when the recommended agent is a new and/or infrequently employed drug.
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