Residue depletion profiles and withdrawal intervals of florfenicol and its metabolite florfenicol amine in plasma and milk of lactating goats after repeated subcutaneous administrations

IF 3 4区 医学 Q1 MEDICINE, LEGAL Regulatory Toxicology and Pharmacology Pub Date : 2024-09-18 DOI:10.1016/j.yrtph.2024.105707
Qiran Chen , Zhoumeng Lin , Jennifer L. Davis , Emily Toney , Maaike O. Clapham , Xue Wu , Lisa A. Tell
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Abstract

Florfenicol is a broad-spectrum and bacteriostatic antibiotic with a time-dependent killing action. It is commonly used to treat respiratory diseases in goats in an extra-label manner. This study aimed to determine the plasma pharmacokinetics and milk residue depletion profiles and calculate the milk withdrawal interval (WDI) of florfenicol and its main metabolite florfenicol amine in lactating goats. Five healthy lactating goats were administered with 40 mg/kg florfenicol by subcutaneous injection, twice, 96 h apart. Plasma and milk samples were collected up to 864 h post the first injection. Non-compartmental analysis was used to estimate the plasma pharmacokinetic parameters. Milk WDIs were calculated using the U.S. Food and Drug Administration (FDA) method and European Medicines Agency (EMA) method. A Monte Carlo simulation was performed to generate simulated data for five virtual animals to meet the data requirement of the FDA method. The calculated milk WDIs based on florfenicol, florfenicol amine, and the combined (the sum of florfenicol and florfenicol amine) were 720.28, 690.45, and 872.69 h after the last injection using the FDA method. In conclusion, this study improves our understanding on the plasma pharmacokinetics and milk residue depletion kinetics of florfenicol and florfenicol amine in lactating ruminants after subcutaneous injections.
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重复皮下注射后哺乳山羊血浆和乳汁中氟苯尼考及其代谢物氟苯尼考胺的残留消耗曲线和停药间隔时间。
氟苯尼考是一种广谱抑菌抗生素,具有时间依赖性杀菌作用。它通常以标签外的方式用于治疗山羊的呼吸道疾病。本研究旨在确定氟苯尼考及其主要代谢物氟苯尼考胺在哺乳山羊体内的血浆药代动力学和乳汁残留消耗曲线,并计算断奶间隔(WDI)。对五只健康的泌乳山羊皮下注射 40 mg/kg 氟苯尼考,两次间隔 96 小时。在第一次注射后的 864 小时内采集血浆和牛奶样本。采用非室分析法估算血浆药代动力学参数。牛奶 WDI 采用美国食品药品管理局 (FDA) 方法和欧洲药品管理局 (EMA) 方法计算。为满足 FDA 方法的数据要求,对五只虚拟动物进行了蒙特卡罗模拟,以生成模拟数据。根据氟苯尼考、氟苯尼考胺和组合(氟苯尼考和氟苯尼考胺之和)计算出的牛奶WDI分别为最后一次注射后的720.28、690.45和872.69小时。总之,本研究加深了我们对泌乳反刍动物皮下注射氟苯尼考和氟苯尼考胺后血浆药代动力学和乳汁残留消耗动力学的了解。
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来源期刊
CiteScore
6.70
自引率
8.80%
发文量
147
审稿时长
58 days
期刊介绍: Regulatory Toxicology and Pharmacology publishes peer reviewed articles that involve the generation, evaluation, and interpretation of experimental animal and human data that are of direct importance and relevance for regulatory authorities with respect to toxicological and pharmacological regulations in society. All peer-reviewed articles that are published should be devoted to improve the protection of human health and environment. Reviews and discussions are welcomed that address legal and/or regulatory decisions with respect to risk assessment and management of toxicological and pharmacological compounds on a scientific basis. It addresses an international readership of scientists, risk assessors and managers, and other professionals active in the field of human and environmental health. Types of peer-reviewed articles published: -Original research articles of relevance for regulatory aspects covering aspects including, but not limited to: 1.Factors influencing human sensitivity 2.Exposure science related to risk assessment 3.Alternative toxicological test methods 4.Frameworks for evaluation and integration of data in regulatory evaluations 5.Harmonization across regulatory agencies 6.Read-across methods and evaluations -Contemporary Reviews on policy related Research issues -Letters to the Editor -Guest Editorials (by Invitation)
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