WebMay 13, 2024 · Salmonid Rickettsial Septicemia (SRS) is the disease of greatest economic importance in the Chilean salmon farming industry, causing high mortality in fish during the final stage of their productive cycle at sea. Since current, commercially available vaccines have not demonstrated the expected efficacy levels, antimicrobials, most commonly … WebOct 15, 2024 · The susceptibility of florfenicol against 28 isolates of Aeromonas salmonicida isolated from diseased lumpfish ranged from 0.39 to 1.56 μg/ml and where three isolates had MIC value of 0.39 μg/ml, 14 isolates MIC value 0.78 μg/ml and 11 isolates MIC value 1.56 μg/ml.. 4. Discussion. Knowledge of pharmacokinetics in lumpfish is …
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WebSep 21, 2024 · environment where fish live, creating a continuous immersion effect and could further pollute their living environment and intoxicate surrounding non-target organisms. This creates a unique concern/feature for approval of medicines in aquatic species because risks associated with inappropriate uses, explicitly tissue residue … WebApr 7, 2024 · Request PDF Pharmacokinetics and depletion of florfenicol in striped catfish Pangasianodon hypophthalmus after oral administration Florfenicol is commonly used to treat bacterial diseases in ... incompatibility definition pharmacology
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WebMar 28, 2011 · The pharmacokinetics of florfenicol (FF) was studied in plasma after a single dose (40 mg/kg) of intramuscular (i.m.) or oral gavage (p.o.) administration to crucian carp (Carassius auratus cuvieri ) in freshwater at 25 °C. Ten fish per sampling point were examined after treatment. Webin the bile (38.25±4.46 h). The AUC tissue/plasma was highest for bile (3.77 ± 0.22), followed by intestine > mus-cle + skin > heart > liver > kidney = gill = spleen. T max and t 1/2β were slower, and max C was lower for FFA than orfenicol in all tissues except max of the kidney and C bile. FFA 1/2β was exceptionally slower in the kidney t WebThe pharmacokinetics of florfenicol (FF) in turbot (Scophthalmus maximus) was studied after single intravenous (10 mg kg −1) and oral (100 mg kg −1) administration. The plasma concentration–time data of florfenicol were described by an open one-compartment model. The elimination half-life (t 1/2) was estimated to be 21.0 h, ... incompatibility chart