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pubmed-article:3095775pubmed:abstractTextCefpiramide (SR 95445) (CPM) is a new cephalosporin with activity against Pseudomonas and a good bioavailability following parenteral administration. This drug is a first rather than second choice treatment in Pseudomonas infections. For this reason, investigation into cefpiramide's capacity to induce beta-lactamase production is especially interesting. A heavy inoculum of P. aeruginosa NCTC 8203, a strain that produces and inducible cephalosporinase (pI = 8.7) was incubated for 4 hours with CPM, cefsulodin (CFS), cefoperazone (CPZ) and ceftazidime (CTZ) in various concentrations. After collection and sonic treatment of the bacteria, the beta-lactamase activity was assayed using an acidimetric method and expressed as units of enzyme activity per mg proteins in the cell-free extract. The smallest increase in beta-lactamase production was recorded with CPM. The strongest inductor was CTZ. CFS and CPZ had an intermediate effect.lld:pubmed
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pubmed-article:3095775pubmed:pagination419-23lld:pubmed
pubmed-article:3095775pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:3095775pubmed:year1986lld:pubmed
pubmed-article:3095775pubmed:articleTitle[Beta-lactamase induction in Pseudomonas aeruginosa by cefpiramide and 3 other antipyocyanic cephalosporins].lld:pubmed
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pubmed-article:3095775pubmed:publicationTypeComparative Studylld:pubmed
pubmed-article:3095775pubmed:publicationTypeEnglish Abstractlld:pubmed