ANTIBACTERIAL ACTIVITY OF CEFPODOXIME PROXETIL IN A PHARMACOKINETIC INVITRO MODEL

被引:15
|
作者
WIEDEMANN, B
JANSEN, A
机构
[1] Pharmaceutical Microbiology, 5300 Bonn 1
关键词
D O I
10.1093/jac/26.1.71
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
The antibacterial activity of cefpodoxime proxetil was studied in an in-vitro model simulating doses of 100, 200 and 400 mg. Strains of Klebsiella spp. Proteus mirabilis, Escherichia coli, Streptococcus pyogenes, and Haemophilus influenzae were effectively reduced by a dose of 200 mg. While for Esch. coli no dose-activity relationship was observed-the maximal effect was achieved with a simulated dose of 100 mg-Staphylococcus aureus could be reduced effectively only by a simulated dose of 400 mg. The lower doses showed stepwise lower activities. Apart from broad spectrum β-lactamases like SHV 2 or TEM 5 the presence of plasmid coded β-lactamases in Esch. coli and H. influenzae did not affect the antibacterial activity of cefpodoxime proxetil. The results show that cefpodoxime was more active against Gram-negative bacteria than amoxycillin, and comparable activity to intramuscular cefotiam in the in-vitro model. © 1990 by The British Society for Antimicrobial Chemotherapy.
引用
收藏
页码:71 / 79
页数:9
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