N. Miyashita et al., IN-VITRO AND IN-VIVO ACTIVITIES OF AM-1155, A NEW FLUOROQUINOLONE, AGAINST CHLAMYDIA SPP, Antimicrobial agents and chemotherapy, 41(6), 1997, pp. 1331-1334
The in vitro and in vivo activities of AM-1155, a new quinolone, again
st Chlamydia spp. were investigated, The MIC of AM-1155 for 10 standar
d strains of different Chlamydia spp. and 25 wild-type strains of Chla
mydia pneumoniae isolated in Japan, which were morphologically differe
nt from clinical isolates from the United States, ranged from 0.063 to
0.125 mu g/ml. Its activity was almost the same as those of sparfloxa
cin and tosufloxacin and was 4 and 16 times superior to those of levof
loxacin and ciprofloxacin, respectively, but lower than those of clari
thromycin and minocycline (range for each, 0.016 to 0.031 mu g/ml). Th
e minimal chlamydiacidal concentration of AM-1155 ranged from 0.063 to
0.125 mu g/ml, while those of clarithromycin and minocycline ranged f
rom 0.016 to 0.031 mu g/ml and 0.016 to 0.063 mu g/ml, respectively, T
he therapeutic effect of a 7-day course of AM-1155 at doses of 5 and 1
0 mg/kg of body weight administered orally twice daily to mice with ex
perimental Chlamydia psittaci pneumonia was excellent, with a 100% sur
vival rate at 21 days after infection, The efficacy was equal to those
of clarithromycin and minocycline and higher than those of ciprofloxa
cin and ofloxacin.