In Vitro and In Vivo Antibacterial Activities of CS-834, a New Oral Carbapenem

Author:

Yamaguchi Keizo1,Domon Haruki1,Miyazaki Shuichi1,Tateda Kazuhiro1,Ohno Akira1,Ishii Kazuhiro1,Matsumoto Tetsuya1,Furuya Nobuhiko1

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

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