Abstract |
In vitro activity of ramoplanin, a cyclic lipoglycopeptide, against 92 vancomycin-resistant gram-positive organisms was evaluated. Ramoplanin demonstrated potent activity against many highly vancomycin-resistant organisms including enterococci (MICs for 90% of strains tested of 0.5 micrograms/ml) and against Lactobacillus spp., Leuconostoc spp., and Pediococcus spp., all of which were inhibited at concentrations of < or = 0.25 micrograms/ml. This drug or a derivative compound merits further investigation as a potential therapeutic agent for infections due to vancomycin-resistant enterococci.
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Authors | L A Collins, G M Eliopoulos, C B Wennersten, M J Ferraro, R C Moellering Jr |
Journal | Antimicrobial agents and chemotherapy
(Antimicrob Agents Chemother)
Vol. 37
Issue 6
Pg. 1364-6
(Jun 1993)
ISSN: 0066-4804 [Print] United States |
PMID | 8328787
(Publication Type: Comparative Study, Journal Article)
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Chemical References |
- Anti-Bacterial Agents
- Depsipeptides
- Peptides, Cyclic
- ramoplanin
- Vancomycin
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Topics |
- Anti-Bacterial Agents
(pharmacology)
- Depsipeptides
- Drug Resistance, Microbial
- Enterococcus
(drug effects)
- Gram-Positive Bacteria
(drug effects)
- Humans
- Kinetics
- Microbial Sensitivity Tests
- Peptides, Cyclic
- Vancomycin
(pharmacology)
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