z-logo
open-access-imgOpen Access
Ceftizoxime (FK 749), a new parenteral cephalosporin: in vitro and in vivo antibacterial activities
Author(s) -
Takuya Kamimura,
Yoshimi Matsumoto,
Naohiko Okada,
Y Mine,
Motohiro Nishida,
Shinichi Goto,
S Kuwahara
Publication year - 1979
Publication title -
antimicrobial agents and chemotherapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.07
H-Index - 259
eISSN - 1070-6283
pISSN - 0066-4804
DOI - 10.1128/aac.16.5.540
Subject(s) - cefmetazole , cefamandole , microbiology and biotechnology , cefotaxime , cefotiam , cephalosporin , ceftizoxime , antibiotics , cefoxitin , cefuroxime , aztreonam , enterobacter , medicine , pharmacology , staphylococcus aureus , chemistry , imipenem , biology , bacteria , antibiotic resistance , escherichia coli , biochemistry , genetics , gene
FK 749 is a new parenteral cephalosporin derivative which is more active against various gram-negative bacilli, including the opportunistic pathogens such as Enterobacter, Citrobacter species, and Serratia marcescens, than cephalosporins and cephamycins such as cefotiam, cefamandole, cefuroxime, cefotaxime, and cefmetazole. FK 749 was especially active against gram-negative organisms resistant to these related antibiotics. FK 749 was more potent in bactericidal activity than the other antibiotics, and the activity was clearly enhanced in the presence of 90% defibrinated rabbit blood. The therapeutic effect of subcutaneously injected FK 749 in mice infected with various gram-negative bacilli was far superior to that of cefotiam, cefamandole, cefuroxime, and cefmetazole and was almost the same as that of cefmetazole in mice infected with Staphylococcus aureus and that of ticarcillin in mice infected with Pseudomonas aeruginosa. FK 749 has, in general, nearly the same in vitro and in vivo antibacterial activities as cefotaxime. The former had more potent bactericidal activity in the presence of the blood than the latter and showed more excellent therapeutic effect than cefotaxime against infections caused by large inoculum sizes.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom