首页> 外文期刊>Food and Chemical Toxicology: An International Journal Published for the British Industrial Biological Research >Development and application of a population physiologically based pharmacokinetic model for florfenicol and its metabolite florfenicol amine in cattle
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Development and application of a population physiologically based pharmacokinetic model for florfenicol and its metabolite florfenicol amine in cattle

机译:氟苯纤维素种群生理基于物理学药代动力学模型及其在牛中的代谢物氟苯钴胺的开发和应用

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摘要

Florfenicol (FF) is used in cattle to treat respiratory diseases but could result in tissue residues. This study aimed to develop a population physiologically based pharmacokinetic (PBPK) model to predict the concentrations of FF and its metabolite, florfenicol amine (FFA), in cattle after four different routes of administration, and to calculate and compare the withdrawal intervals (WDIs) with approved withdrawal times based on different marker residues and their MRLs or tolerances. A flow-limited PBPK model including both FF and FFA sub-models were developed with published data using acslXtreme. This model predicted FF and FFA concentrations in tissues and plasma/serum after intramuscular or subcutaneous administration. Based on the model, the WDIs of 46 and 58 days were calculated to ensure that total residue concentrations (FF + FFA) in 95th percentile of the population after intramuscular and subcutaneous administration were below the MRL, respectively. WDIs were calculated as 44 and 47 days to ensure that FFA concentrations after intramuscular and subcutaneous administration fell below tolerances in 99th percentile of the population, respectively. WDIs were longer than the corresponding label in China, US, and EU. This model provides a useful tool to predict tissue residues of FF and FFA in cattle to improve food safety.
机译:Florfenicol(FF)用于牛治疗呼吸系统疾病,但可能导致组织残留物。本研究旨在开发一种生理基础的药代动力学(PBPK)模型,以预测FF及其代谢物的浓度,氟苯胺胺(FFA)在四种不同的给药之后,并计算和比较戒断间隔(WDI)基于不同标记残留物及其MRL或耐受性的批准的取消时间。流动限制的PBPK模型包括FF和FFA子模型的使用ACSLXTreme与已发布的数据开发。在肌肉内或皮下给药后,该模型预测组织和血浆/血清中的FF和FFA浓度。基于该模型,计算了46和58天的WDI,以确保肌肉内和皮下施用后95百分位数的总残留浓度(FF + FFA)分别在MRL下方。 WDIS计算为44和47天,以确保肌肉内和皮下施用后的FFA浓度分别低于群体的99百分位数的耐受性。 WDIS比中国,美国和欧盟的相应标签长。该模型提供了一种有用的工具,可以在牛中预测FF和FFA的组织残留以改善食品安全性。

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