Abstract
Cefodizime (formerly HR221) was tested either for in vitro microbiological activity or for its stability to beta-lactamases in the presence of two beta-lactamase inhibitors (clavulanic acid, tazobactam). Cefodizime was a poor substrate of class C enzymes but hyperproducer strains were generally resistant with or without a beta-lactamase inhibitor used in combination. On the contrary, class A enzymes were able to hydrolyze cefodizime. However, strains expressing class A beta-lactamase were susceptible to cefodizime in combination with clavulanic acid.
Publication types
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Comparative Study
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Research Support, Non-U.S. Gov't
MeSH terms
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Anti-Bacterial Agents / pharmacology*
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Bacteria / drug effects*
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Cefotaxime / analogs & derivatives*
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Cefotaxime / antagonists & inhibitors
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Cefotaxime / pharmacology
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Clavulanic Acid
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Clavulanic Acids / pharmacology*
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Drug Combinations
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Drug Interactions
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Drug Stability
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Humans
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Microbial Sensitivity Tests
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Penicillanic Acid / pharmacology*
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Tazobactam
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beta-Lactamase Inhibitors*
Substances
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Anti-Bacterial Agents
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Clavulanic Acids
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Drug Combinations
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beta-Lactamase Inhibitors
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Clavulanic Acid
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Penicillanic Acid
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Cefotaxime
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Tazobactam
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cefodizime