Skip Navigation


JAC Advance Access originally published online on October 15, 2004
Journal of Antimicrobial Chemotherapy 2004 54(6):1148-1151; doi:10.1093/jac/dkh463
This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow All Versions of this Article:
54/6/1148    most recent
dkh463v1
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 (10)
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Sevillano, D.
Right arrow Articles by Prieto, J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Sevillano, D.
Right arrow Articles by Prieto, J.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

JAC vol.54 no.6 © The British Society for Antimicrobial Chemotherapy 2004; all rights reserved

Bactericidal activity of amoxicillin against non-susceptible Streptococcus pneumoniae in an in vitro pharmacodynamic model simulating the concentrations obtained with the 2000/125 mg sustained-release co-amoxiclav formulation

David Sevillano1, Almudena Calvo1, María-José Giménez1, Luis Alou1, Lorenzo Aguilar1, Eva Valero1, Antonio Carcas2 and José Prieto1,*

1 Microbiology Department, School of Medicine, Universidad Complutense, Madrid; 2 Pharmacology Unit, Universidad Autónoma, Madrid, Spain

* Corresponding author. Tel: +34-91-3941508; Fax: +34-91-3941511; Email: jprieto{at}med.ucm.es

Objectives: To investigate the bactericidal activity against Streptococcus pneumoniae of simulated amoxicillin serum concentrations obtained in humans after 2000/125 mg sustained-release (SR) and 875/125 mg co-amoxiclav administered twice and three times a day, respectively.

Methods: An in vitro computerized pharmacodynamic simulation was carried out and colony counts were determined over 24 h. Ten strains non-susceptible to amoxicillin (four of them exhibiting an MIC of 4 mg/L, five strains with an MIC of 8 mg/L and one strain with an MIC of 16 mg/L) were used.

Results: With amoxicillin 2000 mg, an initial inoculum reduction >99.99% was obtained for strains with an MIC of 4 mg/L, ≥99% for strains with an MIC of 8 mg/L and 70.6% for the strain with an MIC of 16 mg/L at 24 h sampling time. At this sampling time, no reduction of initial inocula was obtained with amoxicillin 875 mg/8 h for two of the four strains with an MIC of 4 mg/L, three of the five strains with an MIC of 8 mg/L or for the strain with an MIC of 16 mg/L.

Conclusions: The new co-amoxiclav 2000/125 mg SR formulation appears to offer advantages versus previous formulations with respect to bactericidal activity against current amoxicillin non-susceptible strains.

Keywords: ß-lactams , pneumococcal isolates , inocula decrease


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
Antimicrob. Agents Chemother.Home page
M. Torrico, L. Aguilar, N. Gonzalez, M. J. Gimenez, O. Echeverria, F. Cafini, D. Sevillano, L. Alou, P. Coronel, and J. Prieto
Influence of TEM-1 {beta}-Lactamase on the Pharmacodynamic Activity of Simulated Total versus Free-Drug Serum Concentrations of Cefditoren (400 Milligrams) versus Amoxicillin-Clavulanic Acid (2,000/125 Milligrams) against Haemophilus influenzae Strains Exhibiting an N526K Mutation in the ftsI Gene
Antimicrob. Agents Chemother., October 1, 2007; 51(10): 3699 - 3706.
[Abstract] [Full Text] [PDF]


Home page
J Antimicrob ChemotherHome page
L. Alou, M. J. Gimenez, D. Sevillano, L. Aguilar, N. Gonzalez, O. Echeverria, M. Torrico, P. Coronel, and J. Prieto
Are {beta}-lactam breakpoints adequate to define non-susceptibility for all Haemophilus influenzae resistance phenotypes from a pharmacodynamic point of view?
J. Antimicrob. Chemother., April 1, 2007; 59(4): 652 - 657.
[Abstract] [Full Text] [PDF]


Home page
J Antimicrob ChemotherHome page
D. Sevillano, L. Aguilar, L. Alou, M.-J. Gimenez, O. Echevarria, F. Cafini, E. Valero, A. Fenoll, and J. Prieto
Effects of antimicrobials on the competitive growth of Streptococcus pneumoniae: a pharmacodynamic in vitro model approach to selection of resistant populations
J. Antimicrob. Chemother., October 1, 2006; 58(4): 794 - 801.
[Abstract] [Full Text] [PDF]


Home page
J Antimicrob ChemotherHome page
L. Alou, M.-J. Gimenez, D. Sevillano, L. Aguilar, F. Cafini, O. Echeverria, E. Perez-Trallero, and J. Prieto
A pharmacodynamic approach to antimicrobial activity in serum and epithelial lining fluid against in vivo-selected Streptococcus pneumoniae mutants and association with clinical failure in pneumonia
J. Antimicrob. Chemother., August 1, 2006; 58(2): 349 - 358.
[Abstract] [Full Text] [PDF]


Home page
J Antimicrob ChemotherHome page
D. Sevillano, L. Alou, L. Aguilar, O. Echevarria, M.-J. Gimenez, and J. Prieto
Azithromycin iv pharmacodynamic parameters predicting Streptococcus pneumoniae killing in epithelial lining fluid versus serum: an in vitro pharmacodynamic simulation
J. Antimicrob. Chemother., June 1, 2006; 57(6): 1128 - 1133.
[Abstract] [Full Text] [PDF]


Home page
J Antimicrob ChemotherHome page
L. Alou, L. Aguilar, D. Sevillano, M.-J. Gimenez, F. Cafini, E. Valero, M.-T. Relano, and J. Prieto
Urine bactericidal activity against resistant Escherichia coli in an in vitro pharmacodynamic model simulating urine concentrations obtained after 2000/125 mg sustained-release co-amoxiclav and 400 mg norfloxacin administration
J. Antimicrob. Chemother., April 1, 2006; 57(4): 714 - 719.
[Abstract] [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.