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ORAL PRESENTATION / TAM METİN SÖZLÜ SUNUM



                     Artificial Intelligence–Assisted Physiologically Based Pharmacokinetic (PBPK)
                                 Modelling in Veterinary Pharmacology and Toxicology


                        Hikmet Özgün İŞCAN¹                               Abdurrahman AKSOY¹
                                               ,*


                    ¹Department of Veterinary Pharmacology and Toxicology, Faculty of Veterinary
                                Medicine, Ondokuz Mayıs University, Samsun, TÜRKİYE


               * Correspound Author: hikmetozgun.iscan@omu.edu.tr


                     Abstract

                     In recent years, artificial intelligence (AI) and machine learning (ML) have been increasingly
               applied in veterinary medicine for diagnosis, treatment planning, and data analysis. Drug research

               and development also benefit from the predictive power and efficiency of these technologies.
               Physiologically based pharmacokinetic (PBPK) models mathematically simulate the absorption,
               distribution, metabolism, and excretion (ADME) of drugs based on species-specific anatomical

               and  physiological  characteristics.  These  models  are  valuable  tools  for  dose  adjustment,
               interspecies  extrapolation,  evaluation  of  drug–drug  interactions,  and  toxicological  risk
               assessment. Widely used PBPK software platforms include GastroPlus™, PK-Sim®, and Simcyp

               Animal. Such models facilitate the prediction of key pharmacokinetic parameters such as volume
               of distribution and clearance, support model calibration, and enable dose simulations. AI-assisted
               PBPK  approaches  not  only  accelerate  experimental  workflows  but  also  align  with  the  3Rs

               principle,  offering  an  ethical  alternative that reduces  animal  use. The inclination  to  minimize
               animal use, motivated by ethical and economic considerations, has substantially enhanced the
               appeal of these methods. Although PBPK modelling is well established in human medicine, its

               application in veterinary medicine remains limited. This is largely due to the scarcity of species-
               specific physiological data, incomplete databases on transporter proteins and enzyme expression,
               and challenges in model validation. Limited datasets for less-studied species, such as goats or

               exotic  animals,  further  constrain  model  reliability.  In  conclusion,  AI-assisted  PBPK  modelling
               represents  an  innovative,  ethical,  and  scientifically  robust  approach  for  veterinary  drug
               development,  dose  optimisation,  and  toxicological  risk  assessment.  This  methodology  holds

               substantial potential to facilitate the design of individualised treatment strategies and to promote
               safe and effective drug use in veterinary practice.
               Keywords:  Pharmacokinetics;  drug  development;  machine  learning;  veterinary;  artificial

               intelligence.



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