ABSTRACT: 14C-labeled flumequine was administered as a single oral (5 mg kg-1, 86 µCi kg-1) or intravenous (5 mg kg-1, 82 µCi kg-1) dose to Atlantic salmon Salmo salar held in sea water or in fresh water. The absorption, tissue distribution and elimination were determined by means of liquid scintillation counting and whole-body autoradiography. The drug was rapidly absorbed and extensively distributed in all groups of fish. Radiolabeled compound was present in blood and muscle for more than 8 wk in the freshwater groups. In the seawater groups, however, no radioactivity was detected in the blood and muscle after 4 d and 2 wk, respectively. It was concluded that flumequine was eliminated at a substantially higher rate from Atlantic salmon in sea water than in fresh water.
KEY WORDS: Flumequine · Kinetics · Whole-body autoradiography · Atlantic salmon
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