PHARMACOKINETICS OF DIMINAZENE IN PLASMA AND LYMPH OF GOATS

Objective-To characterize the pharmacokinetics of diminazene in plasma and pseudo-afferent lymph of East Africa x Galla goats. Design-The ef ferent prescapular lymphatic duct of 3 goats was cannulated 8 weeks af ter surgical removal of the lymph node. Thereafter, 3.5 mg of diminaze ne base/kg of body weight was administered to these goats and to 3 non cannulated goats. Procedure-Using high-performance liquid chromatograp hy, concentration of diminazene was determined in plasma and lymph col lected up to 96 hours after treatment. Results-Maximal concentrations of diminazene in plasma of noncannulated goats (median [range], 4.30 [ 4.28 to 5.01] mu g/ml), plasma of cannulated goats (3.94 [2.94 to 4.06 ] mu g/ml), and lymph (1.06 [0.73 to 1.86] mu g/ml) were significantly different (P < 0.05); values in lymph were considerably lower than th ose in plasma from noncannulated and cannulated animals. Time to reach maximal concentration did not differ significantly between lymph and plasma of noncannulated and cannulated goats. Over the first 24 hours after drug administration, concentration of diminazene in plasma of no ncannulated goats was generally higher than that in lymph, but thereaf ter was similar. Apparent volume of distribution of diminazene in the plasma of noncannulated (2.57 [1.93 to 2.60] L/kg) and cannulated (2.3 0 [1.04 to 2.40] L/kg) goats did not differ significantly. Penetration ratio of diminazene into lymph, compared with plasma, of cannulated g oals was 1.69:1. Conclusions-Disposition of diminazene in goats is cha racterized by higher concentration in plasma than in lymph. However, t he drug persists longer in lymph than in plasma. Clinical Relevance-Th e longer persistence of diminazene in lymph than in plasma may account for the enhanced therapeutic efficacy of diminazene in the early stag e, compared with later stages, of a tsetse fly-transmitted trypanosome infection.