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We compared the in vitro antimycobacterial activity of a new fluoroquinolone, HSR-903, with strong activity against gram-positive cocci with those of levofloxacin (LVFX), sitafloxacin (STFX), and gatifloxacin (GFLX). The MICs of the quinolones forMycobacterium tuberculosis andMycobacterium avium complex were in the order STFX ≈ GFLX &lt; LVFX ≦ HSR-903 and STFX ≦ GFLX ≦ HSR-903 ≦ LVFX, respectively. HSR-903 effectively eliminated intramacrophagialM. tuberculosis , as did LVFX, and exhibited bacteriostatic effects againstM. tuberculosis replicating in type II alveolar cells.

antimicrobial agents and chemotherapy

Comparative In Vitro Antimicrobial Activities of the Newly Synthesized Quinolone HSR-903, Sitafloxacin (DU-6859a), Gatifloxacin (AM-1155), and Levofloxacin against <i>Mycobacterium tuberculosis</i> and <i>Mycobacterium avium</i> Complex

Comparative In Vitro Antimicrobial Activities of the Newly Synthesized Quinolone HSR-903, Sitafloxacin (DU-6859a), Gatifloxacin (AM-1155), and Levofloxacin against Mycobacterium tuberculosis and Mycobacterium avium Complex