Pradofloxacin: A novel veterinary fluoroquinolone for treatment of bacterial infections in cats

被引:21
|
作者
Sykes, Jane E. [1 ,3 ,4 ]
Blondeau, Joseph M. [2 ,5 ]
机构
[1] Univ Calif Davis, Dept Med & Epidemiol, Davis, CA 95616 USA
[2] Saskatoon Hlth Reg, Royal Univ Hosp, Dept Pathol & Lab Med, Saskatoon, SK S7N 0W8, Canada
[3] Saskatoon Hlth Reg, Royal Univ Hosp, Dept Microbiol & Immunol, Saskatoon, SK S7N 0W8, Canada
[4] Saskatoon Hlth Reg, Royal Univ Hosp, Dept Ophthalmol, Saskatoon, SK S7N 0W8, Canada
[5] Univ Saskatchewan, Saskatoon, SK S7N 0W8, Canada
关键词
Antimicrobial; Minimum inhibitory concentration; Pharmacodynamics; Pharmacokinetics; Resistance; MUTANT PREVENTION CONCENTRATION; STREPTOCOCCUS-PNEUMONIAE; ESCHERICHIA-COLI; RETINAL DEGENERATION; SUSCEPTIBILITY; ENROFLOXACIN; RESISTANCE; SELECTION; AZITHROMYCIN; DOGS;
D O I
10.1016/j.tvjl.2014.06.008
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Pradofloxacin is a novel third-generation oral veterinary fluoroquinolone with activity against Gram-positive aerobic bacteria and anaerobes (lower minimum inhibitory concentrations in vitro). It also has activity against other bacterial species, including Bartonella henselae, Pasteurella multocida, Bordetella bronchiseptica, extra-intestinal Escherichia coli, and some mycobacterial species. This review focuses on the current knowledge of the mechanism of action, adverse effects, clinical applications, and pharmacokinetic/pharmacodynamic properties of pradofloxacin in cats. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:207 / 214
页数:8
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