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
H. Tomioka et al., 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, ANTIM AG CH, 43(12), 1999, pp. 3001-3004
We compared the in vitro antimycobacterial activity of a new fluoroquinolon
e, HSR-903, with strong activity against gram-positive cocci with those of
levofloxacin (LVFX), sitafloxacin (STFX), and gatifloxacin (GFLX). The MICs
of the quinolones for Mycobacterium tuberculosis and Mycobacterium avium c
omplex were in the order STFX approximate to GFLX < LVFX less than or equal
to HSR-903 and STFX less than or equal to GFLX less than or equal to HSR-9
03 less than or equal to LVFX, respectively. HSR-903 effectively eliminated
intramacrophagial M. tuberculosis, as did LVFX, and exhibited bacteriostat
ic effects against M. tuberculosis replicating in type II alveolar cells.