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Beta-lactamase stability of cefoxitin in comparison with other beta-lactam compounds.
- Source :
-
Diagnostic microbiology and infectious disease [Diagn Microbiol Infect Dis] 1983 Dec; Vol. 1 (4), pp. 313-6. - Publication Year :
- 1983
-
Abstract
- The beta-lactamase stability of cefoxitin, the second-generation cephamycin compound, was compared with that of cefamandole, cefoperazone, cefotaxime, moxalactam, carbenicillin, and piperacillin. Unlike cefamandole, cefoperazone, carbenicillin, and piperacillin, cefoxitin was not hydrolyzed by the common plasmid beta-lactamases, TEM-1, TEM-2, OXA-2, and SHV-1. Cefoxitin and moxalactam were the only agents stable to all chromosomal beta-lactamases, whereas cefamandole, cefoperazone, cefotaxime, carbenicillin, and piperacillin were destroyed by cephalosporinases of Proteus vulgaris and Bacteroides fragilis.
- Subjects :
- Carbenicillin metabolism
Cefamandole metabolism
Cefoperazone metabolism
Cefotaxime metabolism
Cephalosporinase metabolism
Gram-Negative Bacteria enzymology
Moxalactam metabolism
Penicillinase metabolism
Piperacillin metabolism
Anti-Bacterial Agents metabolism
Cefoxitin metabolism
beta-Lactamases metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 0732-8893
- Volume :
- 1
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Diagnostic microbiology and infectious disease
- Publication Type :
- Academic Journal
- Accession number :
- 6321094
- Full Text :
- https://doi.org/10.1016/0732-8893(83)90006-8