Teicoplanin, vancomycin, rifampicin: in-vivo and in-vitro studies with Staphylococcus aureus
- 1 May 1987
- journal article
- research article
- Published by Oxford University Press (OUP) in Journal of Antimicrobial Chemotherapy
- Vol. 19 (5) , 659-662
- https://doi.org/10.1093/jac/19.5.659
Abstract
Groups of mice infected with 3.3 × 108Stapyhlococcus aureus via the tail vein were treated three days later with rifampicin (13 mg/kg), vancomycin (33 mg/kg), or teicoplanin (33 mg/kg). Rifampicin was the most effective agent (28 out of 29 survivors). Vancomycin and teicoplanin were of equivalent efficacy (21 of 29 and 24 of 29 survivors, respectively). When intraleucocytic staphylococci were incubated with rifampicin (1 or 20 mg/l), vancomycin (100 mg/l), or teicoplanin (100 mg/l), rifampicin was the most active drug. Vancomycin and teicoplanin were similar.Keywords
This publication has 2 references indexed in Scilit:
- Clinical evaluation of teicoplanin for therapy of severe infections caused by gram-positive bacteriaAntimicrobial Agents and Chemotherapy, 1986
- Teichomycin: in-vitro and in-vivo evaluation in comparison with other antibioticsJournal of Antimicrobial Chemotherapy, 1983