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  • 1
    ISSN: 1439-0426
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: The distribution and residue depletion of thiamphenicol (TAP) were studied in seabass (Dicentrarchus labrax L.) and seabream (Sparus aurata L.) reared in field conditions at temperatures of 20–28 °C. The drug was administered orally as medicated feed at the rate of 40 mg active ingredient (a.i.) kg−1 of biomass once a day for 5 days. Samples of muscle, liver, skin and vertebrae from 10 fishes were collected on the 2nd and 4th day of treatment and 1, 2, 3, 5, 7, 9, 12, 15, 18, 21, 24, 27 and 30 days after the last administration of the drug, and were stored at −20 °C. Quantitative analysis of TAP was performed by high performance liquid chromatography (HPLC) after liquid-liquid extraction; the quantification limits of the HPLC method were 0.02 μg/g for muscle, and 0.05–0.10 μg/g for the other tissues. In seabass, TAP concentrations during treatment were higher in liver and muscle than in skin and vertebrae, and rapidly decreased after the end of medication. Three days after treatment ceased, TAP was still detectable in liver (0.41 ± 0.23 μg/g), vertebrae (0.09 ± 0.03 μg/g) and in three out of 10 samples of muscle (0.03 μg/g), but not in skin. All tissues were below the limits of quantification on the 5th day of withdrawal. In seabream the highest TAP concentrations during treatment were measured in liver and skin, and their reduction after the end of medication was as rapid as that of seabass: on the 3rd day after treatment ceased traces were found in only four out of 10 samples of muscle (0.03 ± 0.00 μg/g) and vertebrae (0.08 ± 0.02 μg/g).
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1573-7446
    Keywords: benzydamine ; bioavailability ; cattle ; milk ; pharmacokinetics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Five lactating cows were given benzydamine hydrochloride by rapid intravenous (0.45 mg/kg) and by intramuscular (0.45 and 1.2 mg/kg) injection in a crossover design. The bioavailability, pharmacokinetic parameters and excretion in milk of benzydamine were evaluated. After intravenous administration, the disposition kinetics of benzydamine was best described using a two-compartment open model. Drug disposition and elimination were fast (t 1/2α: 11.13±3.76 min;t 1/2β: 71.98±24.75 min; MRT 70.69±11.97 min). Benzydamine was widely distributed in the body fluids and tissues (V d(area): 3.549±1.301 L/kg) and characterized by a high value for body clearance (33.00±5.54 ml/kg per min). After intramuscular administration the serum concentration-time curves fitted a one-compartment open model. Following a dose of 0.45 mg/kg, theC max value was 38.13±4.2 ng/ml at at max of 67.13±4.00 min; MAT and MRT were 207.33±22.64 min and 278.01±12.22 min, respectively. Benzydamine bioavailability was very high (92.07%±7.08%). An increased intramuscular dose (1.2 mg/kg) resulted in longer serum persistence (MRT 420.34±86.39 min) of the drug, which was also detectable in milk samples collected from both the first and second milking after treatment.
    Type of Medium: Electronic Resource
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