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두 가지 수온에서 약욕 투여 후 뱀장어(Anguilla japonica)에서의 oxolinic acid 혈청 약동학

Serum pharmacokinetics of oxolinic acid in Japanese eel (Anguilla japonica) after bath treatment at two different water temperatures

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This study investigated the pharmacokinetics of oxolinic acid (OA) in Japanese eel (Anguilla japon- ica) following bath treatment under varying water temperatures and concentrations to support rational antibiotic use and ensure food safety. Eels were exposed to OA at 10 mg/L and 20 mg/L for 12 h at two water temperatures (20℃ and 28℃). Serum OA concentrations were quantified via HPLC- MS/MS at time points ranging from 0.5 to 168 h post-treatment. Pharmacokinetic parameters including elimination half-life (T1/2), maximum serum concentration (Cmax), time to maximum serum concen- tration (Tmax), rea under the concentration-time curve (AUC0–168), and mean residence time (MRT0-168) were calculated using a non-compartmental model. The results demonstrated that OA was eliminated slowly in eels, with marked temperature-dependent differences. In particular, the elimination half-life decreased dramatically with increasing temperature from 231.71–352.20 h at 20℃ to 58.32–96.97 h at 28℃ representing up to a fourfold reduction. Although absorption was slower at higher temperatures (Tmax = 1.5 h at 28℃ vs. 0.5 h at 20℃), systemic exposure increased, as indicated by higher Cmax values (3.35–6.42 µg/mL at 28℃ vs. 2.26–4.69 µg/mL at 20℃). Based on the observed Cmax, the minimum inhibitory concentrations (MIC) required to achieve a Cmax/MIC ≥ 4 were estimated as 0.57-0.84 µg/mL for the 10 mg/L group and 1.17–1.61 µg/mL for the 20 mg/L group. These findings underscore the critical role of water temperature in shaping OA pharmacokinetics and provide valuable baseline data for establishing optimal dosing regimens and withdrawal periods in eel aquaculture.

Abstract

This study investigated the pharmacokinetics of oxolinic acid (OA) in Japanese eel (Anguilla japon- ica) following bath treatment under varying water temperatures and concentrations to support rational antibiotic use and ensure food safety. Eels were exposed to OA at 10 mg/L and 20 mg/L for 12 h at two water temperatures (20℃ and 28℃). Serum OA concentrations were quantified via HPLC- MS/MS at time points ranging from 0.5 to 168 h post-treatment. Pharmacokinetic parameters including elimination half-life (T1/2), maximum serum concentration (Cmax), time to maximum serum concen- tration (Tmax), rea under the concentration-time curve (AUC0–168), and mean residence time (MRT0-168) were calculated using a non-compartmental model. The results demonstrated that OA was eliminated slowly in eels, with marked temperature-dependent differences. In particular, the elimination half-life decreased dramatically with increasing temperature from 231.71–352.20 h at 20℃ to 58.32–96.97 h at 28℃ representing up to a fourfold reduction. Although absorption was slower at higher temperatures (Tmax = 1.5 h at 28℃ vs. 0.5 h at 20℃), systemic exposure increased, as indicated by higher Cmax values (3.35–6.42 µg/mL at 28℃ vs. 2.26–4.69 µg/mL at 20℃). Based on the observed Cmax, the minimum inhibitory concentrations (MIC) required to achieve a Cmax/MIC ≥ 4 were estimated as 0.57-0.84 µg/mL for the 10 mg/L group and 1.17–1.61 µg/mL for the 20 mg/L group. These findings underscore the critical role of water temperature in shaping OA pharmacokinetics and provide valuable baseline data for establishing optimal dosing regimens and withdrawal periods in eel aquaculture.

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