Skip Navigation

This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (3)
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Lacy, M. K.
Right arrow Articles by Quintiliani, R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Lacy, M. K.
Right arrow Articles by Quintiliani, R.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Journal of Antimicrobial Chemotherapy (1999) 44, 477-481
© 1999 The British Society for Antimicrobial Chemotherapy

Protective effect of trovafloxacin, ciprofloxacin and ampicillin against Streptococcus pneumoniaein a murine sepsis model

Melinda K. Lacya, David P. Nicolaub,,c,*, Mary Anne Baneviciusb, Charles H. Nightingaleb,,d and Richard Quintilianib,,d

a Department of Pharmacy Practice, School of Pharmacy, The University of Kansas Medical Center, Kansas City, KS 66160-7231 b Department of Pharmacy Research, Hartford Hospital, Hartford, CT 06102-5037, USA c Division of Infectious Diseases, Hartford Hospital, Hartford, CT 06102-5037, USA d Office of Research Administration, Hartford Hospital, Hartford, CT 06102-5037, USA

Trovafloxacin is a new fluoroquinolone that has potent microbiological activity against the pneumococcus, including penicillin-resistant strains. To evaluate the protective effect of trovafloxacin, ciprofloxacin and ampicillin against penicillin-susceptible, -intermediate and -resistant strains of Streptococcus pneumoniae, an intraperitoneal, immunocompetent mouse model of sepsis was used. The minimum lethal dose (MLD) for each isolate was determined in duplicate. A single sc dose of each antibiotic was administered over a wide range of doses 1 h after the ip inoculation of the test isolate at the MLD. The assessment of the protective dose for 50% of the population (PD50) for each antimicrobial/bacteria combination was performed in triplicate and the PD50 value was calculated at the end of 5 days. Results showed that trovafloxacin provided PD50 values that were significantly lower than those of ciprofloxacin for all isolates. For the penicillin-susceptible and -intermediate isolates, the PD50 values of ampicillin were significantly lower than those for either of the fluoroquinolones studied; however, trovafloxacin was statistically superior to both ciprofloxacin and ampicillin against the penicillin-resistant strain. Therefore, regardless of penicillin susceptibility, trovafloxacin has potent activity against Streptococcus pneumoniae and may be a viable alternative for the treatment of penicillin-resistant isolates.

* Correspondence address. Hartford Hospital, Division of Infectious Diseases, 80 Seymour Street, PO Box 5037, Hartford, CT 06102-5037, USA. Tel: +1-860-545-3941; Fax: +1-860-545-5112; E-mail: dnicola{at}harthosp.org


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Clin. Microbiol. Rev.Home page
D. Chiavolini, G. Pozzi, and S. Ricci
Animal Models of Streptococcus pneumoniae Disease
Clin. Microbiol. Rev., October 1, 2008; 21(4): 666 - 685.
[Abstract] [Full Text] [PDF]


Home page
Antimicrob. Agents Chemother.Home page
S. Sharma, T. N. C. Ramya, A. Surolia, and N. Surolia
Triclosan as a Systemic Antibacterial Agent in a Mouse Model of Acute Bacterial Challenge
Antimicrob. Agents Chemother., December 1, 2003; 47(12): 3859 - 3866.
[Abstract] [Full Text] [PDF]


Home page
The Annals of PharmacotherapyHome page
J. J Schentag, A. K Meagher, and A. Forrest
Fluoroquinolone AUIC Break Points and the Link to Bacterial Killing Rates: Part 1: In Vitro and Animal Models
Ann. Pharmacother., September 1, 2003; 37(9): 1287 - 1298.
[Abstract] [Full Text] [PDF]


Home page
J Antimicrob ChemotherHome page
M. D. Cubbon and R. G. Masterton
New quinolones--a fresh answer to the pneumococcus
J. Antimicrob. Chemother., December 1, 2000; 46(6): 869 - 872.
[Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.