Publication | Closed Access
In vitro and in vivo activities of sparfloxacin, other quinolones, and tetracyclines against Chlamydia trachomatis
33
Citations
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References
1992
Year
C. Trachomatis D/uw-3/cxAntimicrobial SusceptibilityHealth SciencesAntibioticsVivo ActivitiesChlamydia TrachomatisMedicineAntibiotic AdjuvantOther QuinolonesAntibacterial AgentAntimicrobial ChemotherapyMicrobiologyInfection ControlPharmacologyClinical MicrobiologyAntimicrobial ResistanceDrug Resistance
Sparfloxacin was more potent than other quinolones (tosufloxacin, lomefloxacin, ciprofloxacin, ofloxacin, fleroxacin, enoxacin, and norfloxacin) and as potent as minocycline and doxycycline in activity against Chlamydia trachomatis in vitro and in vivo. Sparfloxacin was more bactericidal than minocycline against C. trachomatis D/UW-3/Cx.
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