Affiliation:
1. Department of Microbiological Research, Bristol-Myers Co., Inc., New York, New York 10022
Abstract
Cefadroxil is a new semisynthetic cephalosporin with a broad antibacterial spectrum and a high chemotherapeutic potential when administered orally. The inhibitory activity of this compound was similar to that of cephalexin and cephradine when tested against 602 clinical isolates on Mueller-Hinton medium. In the oral treatment of experimental infections of mice, cefadroxil was more effective than cephalexin against
Streptococcus pyogenes
, and comparably effective against
Streptococcus pneumoniae, Staphylococcus aureus
, and several gram-negative species. Administered orally to mice, at doses ranging from 25 to 100 mg/kg, cefadroxil attained peak concentrations in the blood similar to those of cephalexin. At a dose of 200 mg/kg, however, higher peak levels were noted with cefadroxil than with cephalexin. In regard to other properties which were investigated, the behavior of cefadroxil compared favorably to that of cephalexin.
Publisher
American Society for Microbiology
Subject
Infectious Diseases,Pharmacology (medical),Pharmacology
Reference9 articles.
1. Clark H. and M. Turck. 1969. In vitro and in vivo evaluation of cephalexin p. 296-301. Antimicrob. Agents Chemother. 1968.
2. Kind A. C. D. G. Kestle H. C. Standiford and W. M. M. Kirby. 1969. Laboratory and clinical experience with cephalexin p. 361-365. Antimicrob. Agents Chemother. 1968.
3. Iodometric assay of penicillinase;Perret C. J.;Nature (London),1954
4. Pfeffer M. A. Jackson J. Ximenes and J. P. de Menezes. 1976. Comparative human oral clinical pharmacology of cefadroxil cephalexin and cephradine 11:331-338.
5. Preliminary microbiological and pharmacological evaluation of 6-(R-a-amino-3- thienylacetamido)penicillanic acid (BL-P875);Price K. E.;J. Antibiot. (Tokyo),1969
Cited by
114 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献