Antimicrobial Agents and Chemotherapy · 1988 · 144 citations · 12 references
MedicineMicrobiologyPharmacologyAntimicrobial PharmacologyAntimicrobial PharmacotherapyMedical MicrobiologyAntibacterial PharmacologyAntibacterial PharmacotherapyAntimicrobial Susceptibility TestingBacteroides SpeciesFluoroquinolone AntibioticsPh DependenceUrine Acidification
DR-3355, the S-(-)-isomer of ofloxacin, was generally twice as potent as ofloxacin against a variety of gram-positive and gram-negative pathogens, and its action was bactericidal. The compound was characterized by having the highest level of activity against staphylococci, Bacteroides fragilis, and Peptococcus spp. of the fluorinated quinolones tested, including ofloxacin, ciprofloxacin, fleroxacin, and NY-198. The activity of DR-3355 was not affected by different media, inoculum size, or human serum, but decreased under acidic conditions at pH 5.0 or in human urine.
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In vitro and in vivo activity of DL-8280, a new oxazine derivative
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