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Antimicrobial Agents and Chemotherapy, June 2009, p. 2687-2689, Vol. 53, No. 6
0066-4804/09/$08.00+0 doi:10.1128/AAC.00197-09
Copyright © 2009, American Society for Microbiology. All Rights Reserved.

Targanta Therapeutics Incorporated, 7170 Frederick Banting, St. Laurent, Quebec, Canada H4S 2A1
Received 13 February 2009/ Returned for modification 15 March 2009/ Accepted 29 March 2009
Oritavancin is a lipoglycopeptide with activity against gram-positive pathogens including vancomycin-resistant enterococci. The impact of human serum albumin (HSA) on oritavancin activity against enterococci was compared to those of vancomycin, daptomycin, teicoplanin, and linezolid in vitro using MIC and time-kill methods. Oritavancin MICs increased between 0- and 8-fold in the presence of HSA. In time-kill assays with HSA, oritavancin retained activity, killing or inhibiting enterococci more rapidly than did comparators when peak concentrations were simulated.
Published ahead of print on 6 April 2009.
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