Abstract
Moxalactam (LY127935) exhibited greater in vitro activity than cefamandole and tobramycin against clinical isolates of Enterobacteriaceae, Aeromonas hydrophila, and Pseudomonas maltophilia. The activities of the three drugs against other microorganisms were as follows: for staphylococci, cefamandole = tobramycin greater than moxalactam; for streptococci, cefamandole greater than moxalactam greater than tobramycin; and for Pseudomonas aeruginosa, tobramycin greater than moxalactam greater than cefamandole. Moxalactam also demonstrated significant activity against the Bacteroides fragilis group and other anaerobes. Moxalactam was comparable to cefotaxime (HR756) in its inhibition of cephalothin-resistant and aminoglycoside-resistant clinical isolates.
MeSH Terms
Aminoglycosides/pharmacology
Anti-Bacterial Agents/pharmacology
Bacteria/drug effects
Cefamandole/pharmacology
Cephalosporins/pharmacology
Cephamycins/pharmacology
Drug Resistance, Microbial
Enterobacteriaceae/drug effects
Microbial Sensitivity Tests
Moxalactam
Pseudomonas aeruginosa/drug effects
Staphylococcus/drug effects
Streptococcus/drug effects
Tobramycin/pharmacology
Chemicals
Aminoglycosides
Anti-Bacterial Agents
Cephalosporins
Cephamycins
Cefamandole
Moxalactam
Tobramycin
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Jones R N
Fuchs P C
Sommers H M
Gavan T L
Barry A L
Gerlach E H
References (16)
16 references, click to expand
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