Enrofloxacin pharmacokinetics in yellow catfish (Pelteobagrus fulvidraco): A comparative analysis of oral, intramuscular, and bath administration

IF 1.5 4区 农林科学 Q3 PHARMACOLOGY & PHARMACY
Bofan Jia, Yang Zhao, Jianchao Deng, Shengjun Chen, Chunsheng Li, Bo Qi, Xiao Hu, Laihao Li
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Abstract

Enrofloxacin (ENR) residues in yellow catfish (Pelteobagrus fulvidraco) often exceed the standard due to excessive use. This study explored the pharmacokinetics of ENR and its metabolite ciprofloxacin (CIP) in yellow catfish following a single dose of 10 mg/kg body weight via intramuscular injection (IM), oral gavage (PO), or a 5-h drug bath at 10 mg/L and 25°C. High-performance liquid chromatography-mass spectrometry was used to determine the ENR and CIP concentrations in various tissues. The highest ENR concentration occurred with IM administration, peaking at 4.124 mg/L in the plasma, 8.359 mg/kg in the kidney, 6.272 mg/kg in the liver, and 5.192 mg/kg in the muscle. However, PO administration resulted in the longest metabolic time, with elimination half-lives of 56.47 h in plasma, 86.43 h in the kidney, 76.25 h in the liver, and 64.75 h in muscle. Additionally, the area under the concentration–time curve values for IM, PO, and bath administration in yellow catfish plasma were 108.36, 88.96, and 22.08 mg·h/L, respectively. These results indicate the effectiveness of all three administration methods in treating bacterial diseases in yellow catfish. The selection of an appropriate administration method depends on the minimal inhibitory concentration of ENR against pathogenic bacteria. Yellow catfish subjected to PO and IM administration require longer resting periods before they can be marketed than those receiving drug bath administration.

黄颡鱼的恩诺沙星药代动力学:口服、肌肉注射和浸浴给药的比较分析。
由于过度使用恩诺沙星,黄颡鱼体内的恩诺沙星残留量经常超标。本研究探讨了恩诺沙星及其代谢物环丙沙星(CIP)在黄颡鱼体内的药代动力学,黄颡鱼通过肌肉注射(IM)、口服灌胃(PO)或在 10 mg/L 和 25°C 温度条件下药浴 5 小时,单次剂量为 10 mg/kg 体重。采用高效液相色谱-质谱法测定各种组织中的 ENR 和 CIP 浓度。IM 给药的 ENR 浓度最高,在血浆中达到 4.124 mg/L,在肾脏中达到 8.359 mg/kg,在肝脏中达到 6.272 mg/kg,在肌肉中达到 5.192 mg/kg。不过,口服给药的代谢时间最长,在血浆中的消除半衰期为 56.47 小时,在肾脏中为 86.43 小时,在肝脏中为 76.25 小时,在肌肉中为 64.75 小时。此外,IM、PO 和浸浴给药在黄颡鱼血浆中的浓度-时间曲线下面积值分别为 108.36、88.96 和 22.08 mg-h/L。这些结果表明,这三种给药方法都能有效治疗黄颡鱼的细菌性疾病。选择合适的给药方法取决于 ENR 对病原菌的最小抑制浓度。与接受药浴给药的黄颡鱼相比,接受 PO 和 IM 给药的黄颡鱼需要更长的静养期才能上市。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.10
自引率
15.40%
发文量
69
审稿时长
8-16 weeks
期刊介绍: The Journal of Veterinary Pharmacology and Therapeutics (JVPT) is an international journal devoted to the publication of scientific papers in the basic and clinical aspects of veterinary pharmacology and toxicology, whether the study is in vitro, in vivo, ex vivo or in silico. The Journal is a forum for recent scientific information and developments in the discipline of veterinary pharmacology, including toxicology and therapeutics. Studies that are entirely in vitro will not be considered within the scope of JVPT unless the study has direct relevance to the use of the drug (including toxicants and feed additives) in veterinary species, or that it can be clearly demonstrated that a similar outcome would be expected in vivo. These studies should consider approved or widely used veterinary drugs and/or drugs with broad applicability to veterinary species.
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