Comparative effects of cefpirome (HR 810) and other cephalosporins on experimentally induced pneumonia in mice.

  • KLESEL N.
    Hoechst Aktiengesellschaft, Dept. of Chemotherapy
  • ISERT D.
    Hoechst Aktiengesellschaft, Dept. of Chemotherapy
  • LIMBERT M.
    Hoechst Aktiengesellschaft, Dept. of Chemotherapy
  • SEIBERT G.
    Hoechst Aktiengesellschaft, Dept. of Chemotherapy
  • WINKLER I.
    Hoechst Aktiengesellschaft, Dept. of Chemotherapy
  • SCHRINNER E.
    Hoechst Aktiengesellschaft, Dept. of Chemotherapy

抄録

The chemotherapeutic efficacy of cefpirome (HR 810), a new polar aminothiazolylcephalosporin and that of ceftazidime, cefotaxime, cefoperazone, latamoxef and cefodizime were examined against experimental pneumonia caused by Klebsiella pneumoniae DT-S in mice. When compared in terms of MIC values against the infecting organism and the pharmacokinetic pattern, cefpirome showed equal activity and a similar pharmacokinetic behavior to ceftazidime and cefotaxime in mice. Trials to assess the bactericidial activity in vivo, however, showed that cefpirome displayed a more marked bactericidal effect in pneumonic mice than the other cephalosporins tested. Only cefodizime, a cephalosporin with extremely high and prolonged blood and tissue levels in experimental animals exerted chemotherapeutic effects similar to cefpirome. After cefpirome or cefodizime medication (50mg/kg), the viable counts in the lungs of experimental animals fell steadily to 1/10, 000 of the pretreatment level and, in contrast to the reference compounds, no regrowth of the challenge organisms could be observed with both drugs. Moreover, with ED50s ranging from 1.1 to 59.1mg/kg in treatment studies, cefpirome as well as cefodizime were two to ten times more effective than ceftazidime and cefotaxime, whereas cefoperazone and latamoxef were considerably less effective.

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詳細情報 詳細情報について

  • CRID
    1390282679127095552
  • NII論文ID
    130003409609
  • DOI
    10.7164/antibiotics.39.971
  • ISSN
    18811469
    00218820
  • PubMed
    3531131
  • 本文言語コード
    en
  • データソース種別
    • JaLC
    • Crossref
    • PubMed
    • CiNii Articles
  • 抄録ライセンスフラグ
    使用不可

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