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

Citation
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
Citations number
15
Categorie Soggetti
Pharmacology & Toxicology
Journal title
TOXICOLOGICAL SCIENCES
ISSN journal
10966080 → ACNP
Volume
60
Issue
2
Year of publication
2001
Pages
373 - 378
Database
ISI
SICI code
1096-6080(200104)60:2<373:S(TSO5>2.0.ZU;2-D
Abstract
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.