首页> 外文期刊>Journal of Veterinary Pharmacology and Therapeutics >A physiologically based pharmacokinetics model for florfenicol in crucian carp and oral-to-intramuscular extrapolation.
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A physiologically based pharmacokinetics model for florfenicol in crucian carp and oral-to-intramuscular extrapolation.

机译:cru鱼中氟苯尼考的​​生理基础药代动力学模型和口服至肌内外推法。

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摘要

In this study, an oral physiologically based pharmacokinetics (PBPK) model was developed for florfenicol in crucian carp (Carassius auratus). Subsequently, oral-to-intramuscular extrapolation was performed and the two models were used to predict florfenicol concentrations in the edible tissues of crucian carp. The oral model gave good predictions in most tissues, except for kidney and liver in which the florfenicol concentrations were underestimated at the later time points. In contrast, using the intramuscular model, the concentrations in the kidney were overestimated at the later time points. Both models had the best predictive ability in the main edible tissue, the muscle. The oral model also accurately predicted the florfenicol concentrations in the muscle after multiple doses. The present study demonstrated the feasibility of predicting florfenicol concentrations in the edible tissues of crucian carp using a route-to-route extrapolation method.
机译:在这项研究中,针对cru鱼中的氟苯尼考建立了基于口服生理学的药代动力学(PBPK)模型。随后,进行了从口到肌内的外推法,并使用这两种模型来预测cru鱼可食组织中氟苯尼考的​​浓度。口腔模型在大多数组织中均提供了良好的预测,但肾脏和肝脏中氟苯尼考的​​浓度在随后的时间点被低估了。相反,使用肌内模型,在稍后的时间点高估了肾脏中的浓度。两种模型在主要的可食组织肌肉中具有最佳的预测能力。口服模型还可以准确预测多次服用后肌肉中氟苯尼考的​​浓度。本研究证明了使用逐途径外推法预测cru鱼可食组织中氟苯尼考浓度的可行性。

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