Antimicrobial activity of Ro 23-9424, a novel ester-linked codrug of fleroxacin and desacetylcefotaxime
Open Access
- 1 June 1989
- journal article
- research article
- Published by American Society for Microbiology in Antimicrobial Agents and Chemotherapy
- Vol. 33 (6) , 944-950
- https://doi.org/10.1128/aac.33.6.944
Abstract
Ro 23-9424 is a novel ester-linked codrug of fleroxacin (Ro 23-6240; AM-833) and the cefotaxime metabolite desacetylcefotaxime. Its potency was determined against over 1,000 organisms and found to be intermediate between those of the two components. More than 99% of members of the family Enterobacteriaceae were inhibited by greater than or equal micrograms of Ro 23-9424 per ml; its MIC for 50% of strains tested ranged from greater than or equal to 0.06 to 1 micrograms/ml. Staphylococci, streptococci, Branhamella catarrhalis, Corynebacterium jeikeium, Bacillus spp., Haemophilus influenzae, Listeria monocytogenes, and the pathogenic Neisseria spp., including oxacillin-resistant Staphylococcus aureus, beta-lactamase-producing strains, and penicillin-resistant pneumococci, were also inhibited by Ro 23-9424. Pseudomonas aeruginosa, Enterococcus spp., and Bacteroides fragilis group isolates were more refractory to Ro 23-9424 (the MIC for 90% of strains tested was less than or equal to 32 micrograms/ml). Overall, Ro 23-9424 inhibited 97% of the aerobic strains, compared with 90% for ceftazidime and 92% for cefoperazone. Ro 23-9424 was bactericidal, was relatively stable to inoculum effects on MICs at 10(7) CFU/ml, and was determined to be highly active against organisms resistant to fluoroquinolones or ceftazidime. Preliminary quality control guidelines were determined, and a 30-micrograms disk concentration appears to be the most usable form.This publication has 17 references indexed in Scilit:
- Inactivation of alanine racemase by .beta.-chloro-L-alanine released enzymically from amino acid and peptide C10-esters of deacetylcephalothinBiochemistry, 1987
- In vitro and in vivo antibacterial activity of AM-833, a new quinolone derivativeAntimicrobial Agents and Chemotherapy, 1986
- In vitro activity of Ro 23-6240, a new fluorinated 4-quinoloneAntimicrobial Agents and Chemotherapy, 1986
- Sultamicillin (CP-49, 952): evaluation of two dosage schedules in urinary infectionJournal of Antimicrobial Chemotherapy, 1984
- Pharmacology of Cefuroxime as the 1-acetoxyethyl ester in volunteersAntimicrobial Agents and Chemotherapy, 1984
- Antimicrobial Activity of Desacetylcefotaxime Alone and in Combination with Cefotaxime: Evidence of SynergyClinical Infectious Diseases, 1982
- A three-way crossover study to compare the pharmacokinetics and acceptability of Sultamicillin at two dose levels with that of ampicillinJournal of Antimicrobial Chemotherapy, 1982
- After pro-drugs—mutual pro-drugsJournal of Antimicrobial Chemotherapy, 1981
- Method of reliable determination of minimal lethal antibiotic concentrationsAntimicrobial Agents and Chemotherapy, 1980
- A New Cephalosporin with a Dual Mode of ActionAntimicrobial Agents and Chemotherapy, 1976