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In Vitro Activities of Sitafloxacin (DU-6859a) and Six Other Fluoroquinolones Against 8,796 Clinical Bacterial Isolates

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Specialty Pharmacology
Date 2000 Mar 18
PMID 10722524
Citations 28
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Abstract

The in vitro activities of sitafloxacin, ciprofloxacin, trovafloxacin, levofloxacin, clinafloxacin, gatifloxacin, and moxifloxacin against 5,046 gram-negative bacteria, 3,344 gram-positive cocci, and 406 anaerobes were determined. Sitafloxacin was the most active agent against gram-positive cocci and anaerobes. Against Enterobacteriaceae and nonfermenters, its activity was either equivalent to or better than that of clinafloxacin.

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References
1.
Marshall S, Jones R . In vitro activity of DU-6859a, a new fluorocyclopropyl quinolone. Antimicrob Agents Chemother. 1993; 37(12):2747-53. PMC: 192801. DOI: 10.1128/AAC.37.12.2747. View

2.
Fuchs P, Barry A, Brown S . In vitro activities of clinafloxacin against contemporary clinical bacterial isolates from 10 North American centers. Antimicrob Agents Chemother. 1998; 42(5):1274-7. PMC: 105802. DOI: 10.1128/AAC.42.5.1274. View

3.
Wexler H, Molitoris E, Reeves D, Finegold S . In vitro activity of DU-6859a against anaerobic bacteria. Antimicrob Agents Chemother. 1994; 38(10):2504-9. PMC: 284775. DOI: 10.1128/AAC.38.10.2504. View

4.
Nakashima M, Uematsu T, Kosuge K, Umemura K, Hakusui H, Tanaka M . Pharmacokinetics and tolerance of DU-6859a, a new fluoroquinolone, after single and multiple oral doses in healthy volunteers. Antimicrob Agents Chemother. 1995; 39(1):170-4. PMC: 162504. DOI: 10.1128/AAC.39.1.170. View

5.
Cormican M, Marshall S, Jones R . Cross-resistance analysis for DU-6859a, a new fluoroquinolone, compared to six structurally similar compounds (ciprofloxacin, clinafloxacin, fleroxacin, levofloxacin, ofloxacin, and sparfloxacin). Diagn Microbiol Infect Dis. 1995; 21(1):51-4. DOI: 10.1016/0732-8893(94)00116-e. View