Pharmacokinetics of intravenous and intramuscular danofloxacin in red-eared slider turtles (Trachemys scripta elegans)

被引:8
作者
Corum, Orhan [1 ]
Corum, Duygu Durna [1 ]
Altan, Feray [2 ]
Er, Ayse [3 ]
Cetin, Gul [4 ]
Uney, Kamil [3 ]
机构
[1] Univ Kastamonu, Fac Vet Med, Dept Pharmacol & Toxicol, TR-37200 Kastamonu, Turkey
[2] Dicle Univ, Fac Vet Med, Dept Pharmacol & Toxicol, TR-21280 Diyarbakir, Turkey
[3] Selcuk Univ, Fac Vet Med, Dept Pharmacol & Toxicol, TR-42031 Konya, Turkey
[4] Univ Erzincan, Fac Pharm, Dept Pharmacol, TR-25100 Erzincan, Turkey
关键词
bioavailability; danofloxacin; pharmacokinetics; red-eared slider turtles; PHARMACODYNAMIC INTEGRATION; DEPLETION; TISSUE;
D O I
10.1292/jvms.18-0609
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
This study aimed to investigate the pharmacokinetics of danofloxacin in red-eared slider turtle (Trachemys scripta elegans) following a single intravenous (IV) and intramuscular (IM) administrations of 6 mg/kg, using a two-way crossover study with 30-day washout period. Eight clinically healthy red-eared slider turtle weighing 410-600 g (mean 490 g) were used for the study. Danofloxacin concentrations were measured using the reversed-phase high-performance liquid chromatography. The plasma concentration-time data were evaluated by a non-compartmental method. After IV administration, the elimination half-life (t(1/2 lambda z)), mean residence time (MRT0-8), area under the concentration-time curve (AUC(0-infinity)), volume of distribution at steady state and total body clearance in plasma were 24.17 hr, 30.64 hr, 143.31 hr center dot mu g/ml, 1.29 l/kg and 0.04 l/hr/kg, respectively. Following IM administration, t1/2.z, MRT0-infinity, AUC(0-infinity), peak concentration (C-max), time to reach Cmax, and bioavailability in plasma were 32.00 hr, 41.15 hr, 198.23 hr center dot mu g/ml, 8.75 mu g/ml, 1.5 hr and 139.89%, respectively. Danofloxacin has clinically superior pharmacokinetic properties, including the complete IM absorption, slow elimination and wide volume of distribution in redeared slider turtles. However, further pharmacokinetics/pharmacodynamics studies are necessary for the treatment of diseases caused by susceptible bacteria with known minimum inhibitory concentration values in red-eared slider turtles.
引用
收藏
页码:753 / 757
页数:5
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