THERAPEUTIC EFFICACY OF BENZOXAZINORIFAMYCIN, KRM-1648, IN COMBINATION WITH OTHER ANTIMICROBIALS AGAINST MYCOBACTERIUM-LEPRAE INFECTION-INDUCED IN NUDE-MICE
H. Saito et al., THERAPEUTIC EFFICACY OF BENZOXAZINORIFAMYCIN, KRM-1648, IN COMBINATION WITH OTHER ANTIMICROBIALS AGAINST MYCOBACTERIUM-LEPRAE INFECTION-INDUCED IN NUDE-MICE, International journal of leprosy and other mycobacterial diseases, 62(1), 1994, pp. 43-47
In this study, the in vitro and in vivo anti-Mycobacterium leprae acti
vity of the newly developed benzoxazinorifamycin, KRM-1648, in combina
tion with clofazimine (CFZ) or dapsone (DDS) was evaluated. In vitro a
nti-M. leprae activities of KRM-1648, CFZ, and DDS along with their co
mbinations were measured by the BACTEC 460 TB System. KRM-1648 (0.01 m
u g/ml), CFZ (0.5 mu g/ml), and DDS (2.0 mu g/ml) exhibited a signific
ant anti-M. leprae activity, reducing growth index (GI) values by 78%,
30%, and 35% by day 18, respectively. Combinations of KRM-1648 with e
ither CFZ or DDS, or both caused only a slight increase in the efficac
y. BALB/c nude mice infected subcutaneously with 1 x 10(6) of M. lepra
e Thai-53 strain and test drugs were given to mice by gavage once dail
y six times per week for up to 50 days, from day 31 to day 80. Animals
were observed for the growth of organisms in the hindfoot pad during
the 12 months following infection. KRM-1648 given at the dose of 0.001
mg/mouse exhibited potent antileprosy activity. KRM-1648 exhibited a
significant combined effect with either CFZ or DDS, or both against M.
leprae infection, except that there was no significant difference in
efficacy between KRM-1648 + CFZ and CFZ alone. Furthermore, the effica
cy was most increased in the three-drug regimen KRM-1648 + CFZ + DDS.