Azodicarbonamide: Methods for the analysis in tissues of rats and inhalation disposition

Abstract

1. A method has been developed for measuring azodicarbonamide (ADA) and its metabolite biurea in tissues of rat. The method is based on the reaction of ADA with triphenylphosphine; the derivative so formed was isolated and quantified using reversed-phase h.p.l.c. Quantification was by u.v. detection with ¹⁴C-ADA as internal standard. Biurea was measured by oxidation to ADA, followed by treatment as described above.

2. When biurea was added to tissues at 100–400 μg, recoveries of 92–125% were observed. In contrast, recoveries of ADA added to tissues were generally much less than 100% and could not be reliably determined. The inability to quantify ADA added to tissues was ascribed to its rapid and facile reduction by tissue sulphydryl groups.

3. When rats were exposed to ADA aerosol concentrations of 200, 100, 50 and 0 mg/m³ for 13 weeks by inhalation, a non-linear dose-dependent accumulation of biurea was observed in lungs. No ADA was detected in lungs. Neither biurea nor ADA could be detected in kidneys.