Pharmacokinetics and oral bioavailability of carbimide in man

A pharmacokinetic study of carbimide, an inhibitor of aldehyde dehydrogenase, used as an adjuvant in the aversive therapy of chronic alcoholism, has been carried out in male human volunteers for intravenous and oral administration. Carbimide plasma concentrations were determined by a sensitive and specific high performance liquid chromatographic method. The intravenous doses administered were 0·1, 0·3, 0·6, and 1 mg kg−1 and linear pharmacokinetics were observed for this dose range. Elimination half‐life and total plasma clearance values ranged from 42 to 52 min and from 14·4 to 20·5 ml kg−1 min−1, respectively. After oral administration of 1 and 1·5 mg kg−1 of carbimide, elimination half‐life values were 75 and 61 min, respectively, being higher than the corresponding value obtained after 0·3 mg kg−1 doses, i.e. 39 min. In all cases, rapid absorption was indicated by tmax values ranging from 10·5 to 15·5 min. Absorption was not complete, the oral bioavailability being 53 per cent and 70 per cent for the 0·3 and 1 mg kg−1 carbimide dose, respectively. The data indicate that there is a first‐pass effect for carbimide.