COMPARATIVE ANTIMYCOBACTERIAL ACTIVITIES OF THE NEWLY SYNTHESIZED QUINOLONE AM-1155, SPARFLOXACIN, AND OFLOXACIN
Citation
H. Tomioka et al., COMPARATIVE ANTIMYCOBACTERIAL ACTIVITIES OF THE NEWLY SYNTHESIZED QUINOLONE AM-1155, SPARFLOXACIN, AND OFLOXACIN, Antimicrobial agents and chemotherapy, 37(6), 1993, pp. 1259-1263
Categorie Soggetti
Pharmacology & Pharmacy",Microbiology
SICI code
0066-4804(1993)37:6<1259:CAAOTN>2.0.ZU;2-Y
Abstract
AM-1155 is a newly synthesized 6-fluoro-8-methoxy quinolone. We assess
ed its in vitro antimycobacterial activity using sparfloxacin (SPFX) a
nd ofloxacin (OFLX) as comparison drugs, The MICs of these agents for
various mycobacterial strains were determined by the agar dilution met
hod with 7H11 medium. AM-1155 had lower MICs for 50 and 90% of tested
strains of Mycobacterium kansasii, M. marinum, and M. fortuitum-M. che
lonae complex than SPFX and OFLX, and the values for M. tuberculosis,
M. scrofulaceum, and the M. avium-M. intracellulare complex were simil
ar to those of SPFX and considerably lower than those of OFLX. In addi
tion, the antimicrobial activity of AM-1155 against M. tuberculosis an
d M. intracellulare phagocytosed into murine peritoneal macrophages wa
s compared with that of OFLX. AM-1155 (1 mug/ml) inhibited the intrace
llular growth of both M. tuberculosis and M. intracellulare, whereas O
FLX at the same concentration failed to show any such effect. Moreover
, AM-1155 (10 mug/ml) exhibited a steady bactericidal action against M
. tuberculosis, whereas OFLX at the same concentration had only a weak
effect. AM-1155 (10 mug/ml) also inhibited the growth of M. intracell
ulare more effectively than OFLX.