Abstract |
The in vitro activity of Ro 23-9424 against bacterial isolates from patients with cancer was compared with those of fleroxacin, ciprofloxacin, cefoperazone, and ceftazidime. Ro 23-9424 inhibited the majority of the members of the family Enterobacteriaceae and all Aeromonas isolates at a concentration of less than or equal to 1.0 micrograms/ml. It was also active against Acinetobacter spp. and Haemophilus influenzae, including beta-lactamase-producing strains. The MIC for 90% of isolates (MIC90) of Pseudomonas aeruginosa was 16.0 micrograms/ml. All group A and B streptococci were inhibited by less than or equal to 0.25 micrograms/ml, and 90% of group G streptococci and Streptococcus pneumoniae were inhibited by 1.0 micrograms/ml. All methicillin-susceptible strains of Staphylococcus aureus and 60% of methicillin-resistant strains were susceptible to 2.0 micrograms of Ro 23-9424 per ml, whereas the MIC90 for Staphylococcus epidermidis and Staphylococcus hominis isolates was 4.0 micrograms/ml. Staphylococcus haemolyticus and Enterococcus spp. were less susceptible; MIC90s for them were 16.0 and 32.0 micrograms/ml. Ro 23-9424 has a broad antibacterial spectrum and potential utility for therapy of infections in cancer patients.
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Authors | K V Rolston, H T Nguyen, D H Ho, B LeBlanc, G P Bodey |
Journal | Antimicrobial agents and chemotherapy
(Antimicrob Agents Chemother)
Vol. 36
Issue 4
Pg. 879-82
(Apr 1992)
ISSN: 0066-4804 [Print] United States |
PMID | 1503453
(Publication Type: Comparative Study, Journal Article)
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Chemical References |
- Anti-Infective Agents
- Fluoroquinolones
- Ro-23-9424
- Cefotaxime
- Fleroxacin
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Topics |
- Anti-Infective Agents
(pharmacology)
- Bacteria
(drug effects)
- Cefotaxime
(analogs & derivatives, pharmacology)
- Fleroxacin
(analogs & derivatives, pharmacology)
- Fluoroquinolones
- Humans
- Microbial Sensitivity Tests
- Neoplasms
(microbiology)
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