This work proposes an application of a minimal complexity physiologically based pharmacokinetic model to predict tramadol concentration vs time profiles in horses. Tramadol is an opioid analgesic also used for veterinary treatments. Researchers and medical doctors can profit from the application of mathematical models as supporting tools to optimize the pharmacological treatment of animal species. The proposed model is based on physiology but adopts the minimal compartmental architecture necessary to describe the experimental data. The model features a system of ordinary differential equations, where most of the model parameters are either assigned or individualized for a given horse, using literature data and correlations. Conversely, residual parameters, whose value is unknown, are regressed exploiting experimental data. The model proved capable of simulating pharmacokinetic profiles with accuracy. In addition, it provides further insights on un-observable tramadol data, as for instance tramadol concentration in the liver or hepatic metabolism and renal excretion extent.

A physiologically based model for tramadol pharmacokinetics in horses / R.A. Abbiati, P.P. Cagnardi, G. Ravasio, R.E. Villa, D. Manca. - In: JOURNAL OF THEORETICAL BIOLOGY. - ISSN 0022-5193. - 429(2017 Sep 21), pp. 46-51. [10.1016/j.jtbi.2017.06.028]

A physiologically based model for tramadol pharmacokinetics in horses

P.P. Cagnardi
Secondo
;
G. Ravasio;R.E. Villa
Penultimo
;
2017

Abstract

This work proposes an application of a minimal complexity physiologically based pharmacokinetic model to predict tramadol concentration vs time profiles in horses. Tramadol is an opioid analgesic also used for veterinary treatments. Researchers and medical doctors can profit from the application of mathematical models as supporting tools to optimize the pharmacological treatment of animal species. The proposed model is based on physiology but adopts the minimal compartmental architecture necessary to describe the experimental data. The model features a system of ordinary differential equations, where most of the model parameters are either assigned or individualized for a given horse, using literature data and correlations. Conversely, residual parameters, whose value is unknown, are regressed exploiting experimental data. The model proved capable of simulating pharmacokinetic profiles with accuracy. In addition, it provides further insights on un-observable tramadol data, as for instance tramadol concentration in the liver or hepatic metabolism and renal excretion extent.
Analgesia; Horse; PBPK model; QSP; Tramadol
Settore VET/07 - Farmacologia e Tossicologia Veterinaria
Settore VET/09 - Clinica Chirurgica Veterinaria
21-set-2017
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/511743
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