Some pharmacokinetic parameters of the trypanocidal drug homidium bromide in Friesian and Boran steers using an enzyme-linked immunosorbent assay (ELISA).

Pharmacokinetic studies on the trypanocidal drug homidium bromide using a competitive enzyme immunoassay (detection limit 0.1 ng/mL) are reported for non-infected Friesian and Boran steers following treatment with homidium bromide at a dose of 1.0 mg/kg b.w. Following intravenous (i.v.) treatment of Friesian steers (n=5), the mean serum drug concentrations were 31.9±2.1 and 3.9±0.4 ng/mL at 1 and 24 h, respectively. The decline in serum drug concentration was tri-exponential with half-lives of 0.064±0.037 h for t½α, 7.17±1.87 h for t½β and 106.3±6.6 h for t½γ for distribution and elimination phases 1 and 2, respectively. Drug was detectable in serum for 17 days following treatment. The mean residence time (MRT) was 63.4±7.5 h. Following intramuscular (i.m.) treatment of Friesian steers (n=5), the drug concentration at 1 h after treatment was 72.5±2.2 ng/mL. This declined to 9.8±1.8 ng/mL at 24 h. Low concentrations of between 0.1 and 0.3 ng/mL remained in circulation for up to 90 days post-treatment. Following intramuscular treatment of Boran steers (n=5), the mean serum drug concentration at 1 h after treatment was 112.1±40.3 ng/mL. By 24 h after treatment, the concentration had fallen to 13.0±3.3 ng/mL. Thereafter, the serum drug concentration-versus-time profile and the pharmacokinetic parameters obtained following non-compartmental analysis were similar to those obtained following intramuscular treatment of Friesian steers.