Appelbaum P C
Department of Pathology, Hershey Medical Center, Pennsylvania 17033, USA.
Drugs. 1999;58 Suppl 2:60-4. doi: 10.2165/00003495-199958002-00012.
The first generation of fluoroquinolones such as ciprofloxacin and ofloxacin are inactive against most anaerobic bacteria. However, some broad-spectrum quinolones, which have recently become clinically available or are under active development, have significant antianaerobic activity. This review summarises the in vitro activity of currently available, as well as experimental, quinolones against clinically significant anaerobic bacteria. Quinolones with low activity against anaerobes include ciprofloxacin, ofloxacin, levofloxacin, fleroxacin, pefloxacin, enoxacin and lomefloxacin. Compounds with intermediate antianaerobic activity include sparfloxacin and grepafloxacin. Trovafloxacin, gatifloxacin and moxifloxacin yield low MICs against most groups of anaerobes. Quinolones with the greatest in vitro activity against anaerobes include clinafloxacin and sitafloxacin (DU-6859a).
第一代氟喹诺酮类药物,如环丙沙星和氧氟沙星,对大多数厌氧菌无活性。然而,一些最近已在临床上应用或正在积极研发的广谱喹诺酮类药物具有显著的抗厌氧活性。本综述总结了目前可用的以及实验性喹诺酮类药物对临床上重要厌氧菌的体外活性。对厌氧菌活性低的喹诺酮类药物包括环丙沙星、氧氟沙星、左氧氟沙星、氟罗沙星、培氟沙星、依诺沙星和洛美沙星。具有中等抗厌氧活性的化合物包括司帕沙星和格帕沙星。曲伐沙星、加替沙星和莫西沙星对大多数厌氧菌组的最低抑菌浓度较低。对厌氧菌体外活性最强的喹诺酮类药物包括克林沙星和西他沙星(DU-6859a)。