Affiliation:
1. Department of Microbiology, Toho University School of Medicine, Omori-nishi, 5-21-16, Ota-ku, Tokyo 143, Japan
Abstract
ABSTRACT
CS-834 is a prodrug of the carbapenem R-95867, developed by Sankyo Co., Ltd., Tokyo, Japan. To investigate the possibility that CS-834 may be the first carbapenem usable in an oral dosage form, its in vitro antibacterial activity (as R-95867) and in vivo antibacterial activity were compared with those of cefpodoxime proxetil, cefditoren pivoxil, cefdinir, ofloxacin, imipenem, and amoxicillin. R-95867 had high levels of activity against methicillin-susceptible staphylococci and streptococci, including penicillin-resistant
Streptococcus pneumoniae
, as well as
Neisseria gonorrhoeae
,
Moraxella catarrhalis
, the members of the family
Enterobacteriaceae
(with the exception of
Serratia marcescens
),
Haemophilus influenzae
, and
Bordetella pertussis
; for all these strains, the MICs at which 90% of tested strains are inhibited (MIC
90
s) were 1.0 μg/ml or less. Against methicillin-resistant staphylococci, enterococci,
Serratia marcescens
,
Brukholderia cepacia
,
Stenotrophomonas maltophilia
, and
Acinetobacter calcoaceticus
, R-95867 showed activity comparable to or slightly less than that of imipenem, with MIC
90
s ranging from 2 to >128 μg/ml. The in vivo efficacy of oral CS-834 against experimental mouse septicemia caused by gram-positive and gram-negative bacteria was better than that of comparative drugs. In murine respiratory infection models, the efficacy of CS-834 reflected not only its potent in vitro activity but also the high levels present in the lungs.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Pharmacology (medical),Pharmacology
Cited by
24 articles.
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