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Pharmacokinetics of florfenicol and thiamphenicol in ducks
Marta Tikhomirov1, Błażej Poźniak1, Andrzej Smutkiewicz1
1Department of Pharmacology and Toxicology, Faculty of Veterinary Medicine, Wrocław University of Environmental and Life Sciences, Wrocław, Poland.
Abstract:
The pharmacokinetics of florfenicol (FF) and thiamphenicol (TP) after single intravenous (IV) and oral (PO) administration was investigated in Mulard ducks. Both antibiotics were administered at a dose of 30 mg/kg body weight, and their concentrations in plasma samples were assayed using high-performance liquid chromatography with ultraviolet detection. Pharmacokinetic parameters were calculated using a noncompartmental method. After IV administration, significant differences were found for the mean residence time (2.25 ± 0.21 hr vs. 2.83 ± 0.50 hr for FF and TP, respectively) and the general half-life (1.56 ± 0.15 hr vs. 1.96 ± 0.35 hr for FF and TP, respectively) indicating slightly slower elimination of TP as compared to FF. The clearance, however, was comparable (0.30 ± 0.07 L/hr/kg for FF and 0.26 ± 0.04 L/hr/kg for TP). The mean volume of distribution was below 0.7 L/kg for both drugs. Pharmacokinetics after PO administration was very similar for FF and TP suggesting minor clinical importance of the differences found in the IV study. Both antimicrobials showed rapid absorption and bioavailability of more than 70% indicating that PO route should be an efficient method of FF and TP administration to ducks under field conditions.
Insights
Florfenicol and thiamphenicol exhibit similar pharmacokinetic profiles in ducks, with rapid absorption and high bioavailability via oral administration, suggesting efficient field use for both antimicrobials.
Area of Science:
- Veterinary Pharmacology
- Antimicrobial Pharmacokinetics
- Avian Medicine
Background:
- Florfenicol and thiamphenicol are crucial antimicrobials in veterinary medicine.
- Understanding their pharmacokinetic behavior in ducks is essential for effective therapeutic strategies.
- Mulard ducks are a significant species in poultry production, often requiring antimicrobial treatment.
Purpose of the Study:
- To investigate and compare the pharmacokinetics of florfenicol (FF) and thiamphenicol (TP) in Mulard ducks.
- To evaluate the differences and similarities in drug disposition after intravenous (IV) and oral (PO) administration.
- To determine the suitability of oral administration for field application in ducks.
Main Methods:
- Single IV and PO administration of FF and TP at 30 mg/kg body weight to Mulard ducks.
- Plasma drug concentrations measured using high-performance liquid chromatography with ultraviolet detection.
- Noncompartmental analysis to calculate key pharmacokinetic parameters (e.g., half-life, clearance, volume of distribution, bioavailability).
Main Results:
- After IV administration, thiamphenicol showed a slightly longer mean residence time and half-life compared to florfenicol, indicating slower elimination.
- Drug clearance and volume of distribution were comparable between FF and TP.
- Oral administration revealed highly similar pharmacokinetic profiles for both drugs, with rapid absorption and bioavailability exceeding 70%.
Conclusions:
- Despite minor differences in IV elimination kinetics, florfenicol and thiamphenicol exhibit comparable pharmacokinetic behavior in ducks.
- The high oral bioavailability and rapid absorption support the use of the oral route for efficient administration in field conditions.
- These findings provide valuable data for optimizing antimicrobial therapy in ducks.
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