In vitro activities of five quinolones against Chlamydia pneumoniae.
dc.contributor.author | Hammerschlag, M R | |
dc.contributor.author | Hyman, C L | |
dc.contributor.author | Roblin, P M | |
dc.date.accessioned | 2023-06-26T17:25:35Z | |
dc.date.available | 2023-06-26T17:25:35Z | |
dc.date.issued | 1992-03 | |
dc.identifier.citation | Hammerschlag MR, Hyman CL, Roblin PM. In vitro activities of five quinolones against Chlamydia pneumoniae. Antimicrob Agents Chemother. 1992 Mar;36(3):682-3. doi: 10.1128/AAC.36.3.682. PMID: 1320366; PMCID: PMC190581. | en_US |
dc.identifier.issn | 0066-4804 | |
dc.identifier.pmid | 1320366 | |
dc.identifier.uri | http://hdl.handle.net/20.500.12648/10322 | |
dc.description.abstract | The in vitro susceptibilities of 10 strains of Chlamydia pneumoniae were determined for five quinolones, including ciprofloxacin, ofloxacin, fleroxacin, temafloxacin, and sparfloxacin. Sparfloxacin was the most active compound tested, followed by ofloxacin and temafloxacin. Ciprofloxacin and fleroxacin were the least active. The use of HEp-2 cells for testing C. pneumoniae resulted in larger inclusions but essentially the same endpoints as were seen with use of HeLa 229 cells. | |
dc.language.iso | en | en_US |
dc.relation.url | https://journals.asm.org/doi/10.1128/AAC.36.3.682 | en_US |
dc.rights | Attribution-NonCommercial-NoDerivatives 4.0 International | * |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ | * |
dc.title | In vitro activities of five quinolones against Chlamydia pneumoniae. | en_US |
dc.type | Article/Review | en_US |
dc.source.journaltitle | Antimicrobial agents and chemotherapy | en_US |
dc.source.volume | 36 | |
dc.source.issue | 3 | |
dc.source.beginpage | 682 | |
dc.source.endpage | 3 | |
dc.source.country | United States | |
dc.description.version | VoR | en_US |
refterms.dateFOA | 2023-06-26T17:25:36Z | |
html.description.abstract | The in vitro susceptibilities of 10 strains of Chlamydia pneumoniae were determined for five quinolones, including ciprofloxacin, ofloxacin, fleroxacin, temafloxacin, and sparfloxacin. Sparfloxacin was the most active compound tested, followed by ofloxacin and temafloxacin. Ciprofloxacin and fleroxacin were the least active. The use of HEp-2 cells for testing C. pneumoniae resulted in larger inclusions but essentially the same endpoints as were seen with use of HeLa 229 cells. | |
dc.description.institution | SUNY Downstate | en_US |
dc.description.department | Pediatrics | en_US |
dc.description.degreelevel | N/A | en_US |
dc.identifier.journal | Antimicrobial agents and chemotherapy |