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  2. College of Bioresources and Agriculture / 生物資源暨農學院
  3. School of Veterinary Medicine / 獸醫專業學院
  4. Veterinary Medicine / 獸醫學系
  5. Differential effects of aquatic anaesthetics on the pharmacokinetics of antibiotics: Examples using florfenicol in Nile tilapia (Oreochromis niloticus)
 
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Differential effects of aquatic anaesthetics on the pharmacokinetics of antibiotics: Examples using florfenicol in Nile tilapia (Oreochromis niloticus)

Journal
Journal of Fish Diseases
Journal Volume
44
Journal Issue
10
Pages
1579-1586
Date Issued
2021
Author(s)
Rairat T
Chi Y
SHAO-KUANG CHANG  
Hsieh C.-Y
Chuchird N
Chou C.-C.
DOI
10.1111/jfd.13480
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85108341619&doi=10.1111%2fjfd.13480&partnerID=40&md5=6b1e9fc799ba0872cb703343204d2dfb
https://scholars.lib.ntu.edu.tw/handle/123456789/605988
Abstract
Anaesthetics are commonly applied in pharmacokinetic (PK) studies to assure smooth handling of experimental procedures or to promote animal welfare. However, the influence of anaesthetics on the PK of co-administered drug is generally unknown but assumes ignorable. The goal of the study was to investigate the effect of tricaine methanesulfonate (MS-222), 2-phenoxyethanol (2-PE) and eugenol (EUG) on the PK of florfenicol (FF) in Nile tilapia. Twenty-eight fish were repeatedly exposed to 90?ppm EUG, 300?ppm MS-222 or 900?ppm 2-PE before FF oral administration (15?mg/kg) and each successive blood sampling. The serum concentration–time profiles were analysed by a 2-compartmental model, and the generated parameters in the control (without anaesthetic) and anaesthetic groups were statistically compared. The results demonstrated that the serum concentrations of each anaesthetic were similar at every FF sampling times (70?μg/ml for MS-222; 277?μg/ml for 2-PE; and 61?μg/ml for EUG). In comparison with the control group, the repeated use of MS-222 did not result in a statistical difference in most of the PK parameters. In contrast, the elimination half-lives of the 2-PE and EUG groups were significantly longer whereas the absorption and distribution half-lives of the 2-PE group were significantly shorter than the control, resulting in altered optimal dosages in the simulation modelling. Whether or not the numbers and extent of PK parameters change mitigate subsequent estimations of other PK-derived secondary values such as dosing regimen and withdrawal time remains to be elucidated, but the auxiliary use of anaesthetics in PK studies should not assume uninfluential. ? 2021 John Wiley & Sons Ltd.
Subjects
2-phenoxyethanol
eugenol
florfenicol
MS-222
pharmacokinetics
2 phenoxyethanol
tricaine
aminobenzoic acid derivative
anesthetic agent
antiinfective agent
ethylene glycol derivative
thiamphenicol
animal experiment
Article
blood sampling
compartment model
controlled study
drug absorption
drug blood level
drug distribution
drug half life
high performance liquid chromatography
nonhuman
Oreochromis niloticus
animal
cichlid
physiology
randomization
Aminobenzoates
Anesthetics
Animals
Anti-Bacterial Agents
Cichlids
Ethylene Glycols
Eugenol
Random Allocation
Thiamphenicol
Type
journal article

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