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An assessment of the genetic toxicology of antimony trioxide.

Mutation research (1998-08-26)
B M Elliott, J M Mackay, P Clay, J Ashby
ABSTRACT

Antimony trioxide (Sb2O3, CAS 1309-64-4) has been examined in a range of in vitro and in vivo genotoxicity assays. Negative results were obtained with the Salmonella/microsome assay and the L5178Y mutation assay, but a positive response was observed in the in vitro cytogenetic assay using isolated human peripheral lymphocytes. However, in vivo, antimony trioxide was non-clastogenic in the mouse bone marrow micronucleus assay, following oral gavage administration for 1, 7, 14 or 21 days at dose levels of up to 5000 mg/kg (single dose) or 1000 mg/kg (repeat dose). A negative result was also obtained in the in vivo rat liver DNA repair (unscheduled DNA synthesis) assay following a single oral gavage administration of doses up to 5000 mg/kg. These data show no genotoxicity for antimony trioxide in vivo and do not confirm a previous report of clastogenicity in the mouse on repeated dosing. It is concluded that antimony trioxide is not genotoxic in vivo and does not present a genotoxic hazard to humans.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Antimony(III) oxide, nanopowder, <250 nm particle size (TEM), ≥99.9% trace metals basis
Sigma-Aldrich
Antimony(III) oxide, powder, 5 μm, ReagentPlus®, 99%
Sigma-Aldrich
Antimony(III) oxide, 99.999% trace metals basis
Sigma-Aldrich
Antimony(III) oxide, 99.99% trace metals basis