Pharmacokinetics of sarafloxacin in allogynogenetic silver crucian carp, Carassius auratus gibelio.

Abstract

The pharmacokinetic properties of sarafloxacin were investigated after single intravenous (i.v.) and oral (p.o.) administration of 10 mg/kg body weight (b.w.) in allogynogenetic silver crucian carp at 24-26 °C. The plasma concentrations of sarafloxacin were determined by high-performance liquid chromatography. After i.v. administration, the plasma concentration-time data were described by an open two-compartment model. The elimination half-life (T(1/2β)) was estimated to be 22.58 h. The volume of distribution, V(d(area)), was estimated to be 5.95 L/kg, indicating good tissue penetration of sarafloxacin in the fish. Area under the concentration-time curve (AUC) and total body clearance of sarafloxacin were 56.86 µg·h/mL and 0.18 L/h/kg, respectively. Following p.o. administration, the maximum plasma concentration (C(max)), T(1/2β), and AUC of sarafloxacin were 0.79 µg/mL, 46.68 h, and 16.58 µg·h/mL, respectively. Absorption of the drug was not good with a bioavailability (F) of 29.15%. Based on a minimum inhibitory concentration (MIC) of 0.00625 to 0.045 μg/mL for susceptible strains, sarafloxacin p.o. administration at a dose 10 mg/kg could be efficacious against common pathogenic bacteria of fish.

• Authors: Xingxing Fang, Jianguo Zhou, Xiuhong Liu
• Journal: Fish physiology and biochemistry (Fish Physiol Biochem) Vol. 42 Issue 1 Pg. 335-41 (Feb 2016) ISSN: 1573-5168 [Electronic] Netherlands
• PMID: 26563280 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Anti-Bacterial Agents
• Ciprofloxacin
• sarafloxacin

Topics

• Administration, Intravenous
• Administration, Oral
• Animals
• Anti-Bacterial Agents (administration & dosage, blood, pharmacokinetics)
• Biological Availability
• Carps (blood, metabolism)
• Ciprofloxacin (administration & dosage, analogs & derivatives, blood, pharmacokinetics)
• Models, Biological