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- W2000821551 abstract "A 7H9 broth microdilution method against CI-960, sparfloxacin, WIN57273, ciprofloxacin, norfloxacin, isepamicin, amikacin, kanamycin, ethambutol, isoniazid, and rifampin was used to test 35 Mycobacterium avium-intracellulare complex (MAI) and five M. chelonae-fortuitum strains. The majority of MAI isolates were inhibited by all tested compounds, with sparfloxacin (MIC90, 0.5 μg/ml) being the most active among the fluoroquinolones; isepamicin (MIC90, 4 μg/ml), the most potent aminoglycoside; and isoniazid, rifampin, and ethambutol also demonstrating some degree of activity. Mycobacterium chelonae strains were resistant to all drugs except ciprofloxacin (MIC50, 1 μg/ml). Mycobacterium fortuitum isolates were generally susceptible, especially to the newer fluoroquinolones." @default.
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- W2000821551 date "1992-02-01" @default.
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- W2000821551 title "CI-960 (PD127391 or AM-1091), sparfloxacin, WIN 57273, and isepamicin activity against clinical isolates of Mycobacterium avium-intracellularae complex, M. chelonae, and M. fortuitum" @default.
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- W2000821551 doi "https://doi.org/10.1016/0732-8893(92)90044-t" @default.
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