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Antimicrobial Agents and Chemotherapy, June 2000, p. 1720-1724, Vol. 44, No. 6
Departments of Medicine and Pathology, Beth
Israel Deaconess Medical Center,1 and
Harvard Medical School,2 Boston,
Massachusetts 02115, and Wallace Laboratories, Cranbury, New
Jersey 085123
Received 30 August 1999/Returned for modification 24 November
1999/Accepted 21 March 2000
In vitro, the antimicrobial agent taurolidine inhibited virtually
all of the bacteria tested, including vancomycin-resistant enterococci,
oxacillin-resistant staphylococci, and Stenotrophomonas maltophilia, at concentrations between 250 and 2,000 µg/ml.
Taurolidine was not effective in experimental endocarditis. While it
appears unlikely that this antimicrobial would be useful for systemic therapy, its bactericidal activity and the resistance rates found (<10
0066-4804/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Activities of Taurolidine In Vitro and in
Experimental Enterococcal Endocarditis
9) are favorable indicators for its possible
development for topical use.
*
Corresponding author. Mailing address: Department of
Medicine, Beth Israel Deaconess Medical Center, 110 Francis St., Suite 6A, Boston, MA 02215. Phone: (617) 632-8586. Fax: (617) 632-7442. E-mail: geliopou{at}caregroup.harvard.edu.
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