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Antimicrobial Agents and Chemotherapy, December 1999, p. 2873-2876, Vol. 43, No. 12
Department of Medicine, Beth Israel Deaconess
Medical Center, Boston, Massachusetts 02215, and Harvard Medical
School, Boston, Massachusetts 02115
Received 27 August 1998/Returned for modification 29 March
1999/Accepted 14 September 1999
The in vivo effectiveness of oxazolidinones eperezolid (U-100592)
and linezolid (U-100766) against one strain each of
Enterococcus faecalis and vancomycin-resistant
Enterococcus faecium was examined in a rat model of
intra-abdominal abscess. MICs of both drugs were 2 µg/ml
for each strain. At doses of 25 mg/kg of body weight twice daily
intravenously or orally, linezolid produced small but statistically
significant reductions in abscess bacterial density for E. faecalis. The reduction in viable cells observed would not likely
be clinically relevant. Eperezolid was ineffective at this dose.
At a dosage of 100 mg/kg/day, linezolid treatment led to an
approximately 100-fold reduction in viable cells per gram of
abscess. Against E. faecium infections, intravenous
eperezolid and oral linezolid were effective, reducing densities
approximately 2 log10 CFU/g. Both oxazolidinones
demonstrated activity against enterococci in this model.
However, results were modest with the dosing regimens employed.
0066-4804/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Activities of the Oxazolidinones Linezolid and Eperezolid in
Experimental Intra-Abdominal Abscess Due to Enterococcus
faecalis or Vancomycin-Resistant Enterococcus
faecium
*
Corresponding author. Mailing address: Department of
Medicine
West Campus, Beth Israel Deaconess Medical Center, One
Deaconess Rd., Boston, MA 02215. Phone: (617) 632-8586. Fax: (617)
632-7442. E-mail: geliopou{at}caregroup.harvard.edu.
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