Short-term (13-week) toxicity study of 5-bromo-6-methoxy-5,6-dihydro-3 '-azidothymidine-5 '-(p-bromophenyl) methoxyalaninyl phosphate (WHI-07), a novel anti-HIV and contraceptive agent, in B6C3F1 mice
Oj. D'Cruz et Fm. Uckun, Short-term (13-week) toxicity study of 5-bromo-6-methoxy-5,6-dihydro-3 '-azidothymidine-5 '-(p-bromophenyl) methoxyalaninyl phosphate (WHI-07), a novel anti-HIV and contraceptive agent, in B6C3F1 mice, TOXICOL SCI, 60(2), 2001, pp. 373-378
The zidovudine derivative, WHI-07 (5-bromo-6-methoxy-5,6-dihydro3'-azidothy
midine-5'-(p-bromophenyl) methoxyalaninyl phosphate), is a dual-function sp
ermicidal agent with potent anti-HIV activity. In this study, groups of 20
female B6C3F1 mice were exposed intravaginally to a gel microemulsion conta
ining 0, 0.5, 1.0, or 2.0% WHI-07, 5 days per week for 13 consecutive weeks
. On a molar basis, these concentrations of WHI-07 are 1400- to 5700-times
higher than its spermicidal ECS, and 1.4 x 10(6) to 5.7 x 106 times higher
than its in vitro anti-HIV IC50. After 13 weeks of intravaginal treatment,
mice were evaluated for toxicity. The endpoints that were used for evaluati
on included survival, body weight, hematologic and clinical chemistry profi
les, absolute and relative organ weights, and histopathology. No effects re
lated to WHI-07 treatments were observed on survival, mean body weight, and
mean body-weight gain. Repeated intravaginal exposure of mice to WKI-07 fo
r 13 weeks had no toxicologically significant effect on organ weights, and
did not cause any adverse changes in hematology parameters or blood chemist
ry profiles. Extensive histopathologic examination of tissues showed no les
ions of pathologic significance. Thus, intravaginal application of WHI-07,
for up to 13 weeks, does not cause systemic toxicity.