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Subchronic and Chronic Inhalation Toxicity of Antimony Trioxide in the Rat
Authors:NEWTON, PAUL E.   BOLTE, HENRY F.   DALY, IRA W.   PILLSBURY, BRIAN D.   TERRJLL, JAMES B.   DREW, ROBERT T.   BEN-DYKE, ROGER   SHELDON, ARTHUR W.   RUBIN, LIONEL F.
Affiliation:*Pharmaco LSR Inc. P.O. Box 2360, Mettlers Road, East Millstone, New Jersey 08875-2360 "{dagger}"American Petroleum Institute 1220 L Street, NW, Washington, DC 20005 "{ddagger}"Anlimony Oxide Industry Association Suite 1300, 1001 Pennsylvania Avenue, Washington, DC 20004-2505 "§"University of Pennsylvania 34 th and Spruce Street, Philadelphia, Pennsylvania 19104

Received June 8, 1992; accepted December 7, 1993

Abstract:Fischer 344 rats were exposed by inhalation to Sb2O3 (antimonytrioxide) dust at exposure levels of 0, 0.25, 1.08, 4.92, and23.46 mg/m3 for 6 hr/day, 5 days/week for 13 weeks followedby a 27-week observation period. Subsequently, an inhalationon-cogenicity study was conducted at exposure levels of 0, 0.06,0.51, and 4.50 mg/m3 for 12 months followed by a 12-month observationperiod. The Sb2O3 in the subchronic study had a mass medianaerodynamic diameter (MMAD) of 3.05 ± 0.21 microns (mean± SD) with a geometric standard deviation (GSD) of 1.57± 0.06. In the chronic study, the MMAD was 3.76 ±0.84 and the GSD was 1.79 ± 0.32. Except for the eyes,no adverse clinical observations were attributed to Sb2O3 ineither study. In the subchronic study, corneal irregularitieswere seen after about 2 weeks of exposure and did not abateduring the observation period. In the chronic study, ophthalmoscopicevaluation at 24 months revealed a dose-related increase incataracts of 11, 24, 28, and 32% (both sexes combined) for eachgroup, respectively. Body weights were significantly lower (6%)than the control group's weights in the 23.46 mg/m3 males inthe subchronic study. These rats did not recover this weightduring the 27-week observation period. Body weights of the femalesin both studies and males in the chronic study were unaffected.There were no Sb2O3 effects on clinical chemistry or he-matologyin either study. Mean absolute and relative lung weights weresignificantly increased in the 4.92 and 23.46 mg/m3 groups inthe subchronic study. The 23.46 mg/m3 group's lung weights didnot recover to control levels during the 27-week observationperiod. Lung weights for rats in the chronic study were unaffected.Microscopic changes in the lungs in the subchronic and chronicstudy were limited to subacute-chronic interstitial inflammation,increased numbers of alveolar-in-traalveolar macrophages, foreignmaterial in the alveolar-in-traalveolar macrophages in the peribronchialand perivascular (chronic study only) lymphoid aggregates andin the peribronchial lymph nodes, granulomatous inflammation/granulomas,and fibrosis. In the chronic study, any observed neoplasms occurredwith comparable incidence among all groups and were within thehistorical range for controls. Clearance of Sb2O3 from the lungwas burden dependent and was reduced by 80/ in the 4.50 mg/m3group in the chronic study. The previously reported studies,which found Sb2O3 to be a carcinogen, were run at higher lungburdens. Under the exposure conditions of the current study,Sb2O3 was not a carcinogen.
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