Pharmacokinetics and tissue behavior of enrofloxacin and its metabolite ciprofloxacin in turbot Scophthalmus maximus at two water temperatures

Junping Liang; Jian Li; Fazhen Zhao; Ping Liu; Zhiqiang Chang

doi:10.1007/s00343-012-1228-2

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Pharmacokinetics and tissue behavior of enrofloxacin and its metabolite ciprofloxacin in turbot Scophthalmus maximus at two water temperatures

Updated：2023-05-16

- Pharmacokinetics and tissue behavior of enrofloxacin and its metabolite ciprofloxacin in turbot Scophthalmus maximus at two water temperatures
- Journal of Oceanology and Limnology Vol. 30, Issue 4, Pages: 644-653(2012)
- Affiliations：
  
  1. Fisheries College Ocean University of China
  2. Key Laboratory of Sustainable Development of Marine Fisheries Ministry of Agriculture Yellow Sea Fisheries Research Institute Chinese Academy of Fishery Sciences
- Author bio：
- Funds：
- DOI：10.1007/s00343-012-1228-2
  CLC：
- Online First：02 July 2012，
  
  Published：2012
- Accepted：
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Liang, J., Li, J., Zhao, F. et al. Pharmacokinetics and tissue behavior of enrofloxacin and its metabolite ciprofloxacin in turbot Scophthalmus maximus at two water temperatures., Chin. J. Ocean. Limnol. 30, 644–653 (2012). https://doi.org/10.1007/s00343-012-1228-2
DOI：

Liang, J., Li, J., Zhao, F. et al. Pharmacokinetics and tissue behavior of enrofloxacin and its metabolite ciprofloxacin in turbot Scophthalmus maximus at two water temperatures., Chin. J. Ocean. Limnol. 30, 644–653 (2012). https://doi.org/10.1007/s00343-012-1228-2 DOI：

摘要

Abstract

Turbot Scophthalmus maximus

an important aquaculture species in China

currently suffers from epizootic diseases because of high density aquaculture. Enrofloxacin has been used to treat various systemic bacterial fish infections. However

studies concerning the pharmacokinetics of enrofloxacin in turbot are limited. In this study

the pharmacokinetics of enrofloxacin and its metabolite ciprofloxacin

were investigated in the turbot following intravenous and oral administration at 10 mg enrofloxacin/kg body weight

at 16°C and 10°C water temperatures. The concentrations of enrofloxacin and ciprofloxacin in the main tissues (plasma

muscle

liver and kidney) were detected by HPLC. The results show that the plasma concentration-time data for enrofloxacin were best described as a two-compartment open model after intravenous and oral administration. Three pharmacokinetic equations were established between the concentrations and temperatures. The kinetic profile of enrofloxacin was temperature dependent. The absorption half-life of enrofloxacin was 1.99 h and 2.17 h after oral administration

whereas the elimination half-life of the drug was 98.63 h and 136.59 h at 16°C and 10°C

respectively. The peak concentration of enrofloxacin in plasma and tissues was higher at 16°C than that at 10°C

and the peak plasma concentration time in the liver was the shortest at both temperatures among those of other tissues. The plasma C max /MIC ratio varied between 11.08 and 5 540.00 at 16°C; and between 7.92 and 3 960.00 at 10°C. The AUC/MIC ratio was 467.82–280 690.00 at 16°C

and 359.48–215 690.00 at 10°C. These ratios indicate that it is possible to obtain therapeutic efficacy. Very low levels of ciprofloxacin were detected. The AUC ratios of ciprofloxacin and enrofloxacin in plasma suggest that plasma ciprofloxacin might play a minor role in enrofloxacin treatment for turbot.

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references

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