Depletion of tilmicosin residue in Gushi chickens following oral administration via drinking water

IF 1.5 4区 农林科学 Q3 PHARMACOLOGY & PHARMACY
Mei Zhang, Kun Qian, Guang-Hui Li, Ming-Hui Duan, Ze-En Li, Yan Dai, Jun-Cheng Chen, Fan Yang
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Abstract

This study aimed to examine the depletion of tilmicosin residues in Gushi chickens following the administration at a concentration of 75 mg/L in their drinking water for three consecutive days. Plasma, liver, kidney, lung, muscle, and skin + fat samples were collected from 6 chickens at 6 h, 1, 3, 5, and 7 days after the treatment. Tilmicosin concentrations in the samples were determined using a high-performance liquid chromatography (HPLC) method. The findings revealed that the highest tilmicosin residues were detected in the liver, followed by the kidney, lung, skin + fat, muscle, and plasma. Notably, at 7 days post-treatment, no drug residue was detected in all samples except for the liver and kidney. The non-compartmental model was employed to calculate relevant pharmacokinetic parameters. The elimination half-lives (t1/2λz) of tilmicosin were as follows, ranked from long to short: skin + fat (45.42 h), liver (44.17 h), kidney (40.06 h), plasma (37.64 h), lung (31.39 h), and muscle (30.05 h). Considering the current residue depletion and the maximum residue limits (MRLs) set by Chinese regulatory authorities, the withdrawal times for tilmicosin were estimated as 18.91, 10.81, and 8.58 days in the kidney, liver, and skin + fat, respectively. A rounded-up value of 19 days was selected as the conclusive withdrawal time. Furthermore, based on the observed tilmicosin concentrations in plasma and lung, combined with previously reported minimum inhibitory concentration (MIC) values against Mycoplasma gallisepticum, the current dosing regimen was deemed adequate for treating Mycoplasma gallisepticum infections in Gushi chickens.

谷氏鸡饮水口服替米考星残留量的测定。
本研究旨在检测浓度为75的替米考星在固始鸡体内的残留量 mg/L,连续三天。血浆、肝、肾、肺、肌肉和皮肤 + 从6只鸡身上采集脂肪样本 h、 1、3、5和7 治疗后几天。采用高效液相色谱法测定样品中替米考星的浓度。研究结果显示,替米考星残留量最高的是肝脏,其次是肾脏、肺部和皮肤 + 脂肪、肌肉和血浆。值得注意的是,在7 治疗后几天,除肝脏和肾脏外,所有样本均未检测到药物残留。采用非房室模型计算相关的药代动力学参数。替米考星的消除半衰期(t1/2λz)如下,从长到短排列:皮肤 + 脂肪(45.42 h) ,肝脏(44.17 h) ,肾脏(40.06 h) ,血浆(37.64 h) ,肺(31.39 h) ,和肌肉(30.05 h) 。考虑到目前的残留损耗和中国监管机构设定的最大残留限量,替米考星的停药时间估计为18.91、10.81和8.58 肾脏、肝脏和皮肤的天数 + 脂肪。四舍五入值19 选择天作为最终退出时间。此外,根据观察到的血浆和肺部替米考星浓度,结合先前报道的对鸡毒支原体的最低抑制浓度(MIC)值,目前的给药方案被认为足以治疗固始鸡的鸡毒支原体感染。
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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