PHARMACOKINETICS AND TISSUE PENETRATION OF CEFPROZIL

被引:17
作者
NYE, K [1 ]
ONEILL, P [1 ]
ANDREWS, JM [1 ]
WISE, R [1 ]
机构
[1] DUDLEY RD GEN HOSP,DEPT MED MICROBIOL,BIRMINGHAM B18 7QH,W MIDLANDS,ENGLAND
关键词
D O I
10.1093/jac/25.5.831
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
The pharmacokinetics of cefprozil after a single 500 mg oral dose were studied, measuring plasma, inflammatory fluid and urine concentrations.Mean peak plasma concentrations of 9.6mg/l (measured by bioassay) were achieved at a mean time of 1.9 h after administration. The mean plasma elimination half-life was 1.4 h; 63.6% of the dose was eliminated in urine by 24 h. Mean peak levels in inflammatory fluid reached 4.9 mg/l after 3.5 h.Mean plasma levels remained 2 mg/l for almost 5 h post dose and more than 6 h in inflammatory fluid. These data suggest that infections caused by highly susceptible pathogens might respond to a twice dairy dosing regimen and less susceptible pathogens might require a higher dose or more frequent administration. © 1990 The British Society for Antimicrobial Chemotherapy.
引用
收藏
页码:831 / 835
页数:5
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