tetracycline and lomefloxacin

tetracycline has been researched along with lomefloxacin* in 3 studies

Trials

1 trial(s) available for tetracycline and lomefloxacin

ArticleYear
Multicenter in vitro evaluation of lomefloxacin (NY-198, SC-47111), including tests against nearly 7,000 bacterial isolates and preliminary recommendations for susceptibility testing.
    Diagnostic microbiology and infectious disease, 1988, Volume: 10, Issue:4

    Lomefloxacin (NY-198 or SC-47111) is a difluoro-quinolone derivative having a C-methyl at the 3-position of the piperazine ring, thus minimizing its metabolic alteration in vivo. In our research, its antimicrobial activity was most similar to that of difloxacin, enoxacin, fleroxacin, and norfloxacin but usually less than that of ciprofloxacin and ofloxacin against most species. Lomefloxacin shared cross-resistance with other 4-quinolones but remained very active against ceftazidime-resistant organisms, including stably derepressed beta-lactamase producing Gram-negative bacilli. Lower pH increased the lomefloxacin MICs. MBCs were usually identical to the measured MIC, and the lomefloxacin MICs were not significantly increased by high inoculum concentrations. The Enterobacteriaceae were found to have a very low rate of spontaneous mutation to lomefloxacin resistance (10(-8)-10(-9). In vitro tests by 5-micrograms and 10-micrograms lomefloxacin disks and dilution methods were correlated, and the 10-micrograms disk was recommended for clinical trials using a less than or equal to 4 micrograms/ml susceptible breakpoint. The quality assurance guidelines for dilution tests were determined by a multilaboratory study.

    Topics: 4-Quinolones; Anti-Infective Agents; Bacteria; Drug Resistance, Microbial; Fluoroquinolones; Microbial Sensitivity Tests; Multicenter Studies as Topic; Mutation; Penicillins; Quinolones; Statistics as Topic; Tetracycline

1988

Other Studies

2 other study(ies) available for tetracycline and lomefloxacin

ArticleYear
Susceptibility of Mycoplasma pneumoniae to several new quinolones, tetracycline, and erythromycin.
    Antimicrobial agents and chemotherapy, 1991, Volume: 35, Issue:3

    Mycoplasma pneumoniae (39 strains) was most susceptible to two quinolones, WIN 57273 and sparfloxacin, with MICs for 90% of the strains (MIC90S) of 0.125 and 0.25 micrograms/ml, respectively. It was susceptible to ofloxacin and ciprofloxacin at 2 micrograms/ml and to lomefloxacin and fleroxacin at 4 micrograms/ml. The MIC90 of erythromycin was 0.062 microgram/ml, and that of tetracycline was 1 microgram/ml.

    Topics: Anti-Infective Agents; Erythromycin; Fluoroquinolones; Microbial Sensitivity Tests; Mycoplasma pneumoniae; Ofloxacin; Quinolones; Tetracycline

1991
In vitro activities of lomefloxacin, tetracycline, penicillin, spectinomycin, and ceftriaxone against Neisseria gonorrhoeae and Chlamydia trachomatis.
    Antimicrobial agents and chemotherapy, 1989, Volume: 33, Issue:12

    In vitro lomefloxacin was highly active against 208 penicillin-susceptible and -resistant isolates of Neisseria gonorrhoeae. However, its MIC and MBC against 10 isolates of Chlamydia trachomatis were 2 and greater than 4 micrograms/ml, respectively.

    Topics: 4-Quinolones; Anti-Bacterial Agents; Anti-Infective Agents; Ceftriaxone; Chlamydia trachomatis; Fluoroquinolones; Microbial Sensitivity Tests; Neisseria gonorrhoeae; Penicillins; Quinolones; Spectinomycin; Tetracycline

1989