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POSTER PRESENTATION / POSTER SUNUM



                                  Physiologically-Based Pharmacokinetic Studies in Drug
                              Discovery and Development: The Zebrafish (Danio Rerio)     Model


                                Sultan Nurhan AYIKOL                       Ender YARSAN *
                                                                                          2,
                                                       1

                1 Ankara University, Graduate School of Health Sciences, Department of Pharmacology and
                                                    Toxicology, TÜRKIYE

                   2 Ankara University, Faculty of Veterinary Medicine, Department of Pharmacology and
                                                    Toxicology, TÜRKIYE

               *Correspound Author: eyarsan@gmail.com

                     Zebrafish (Danio rerio) are increasingly being used as a complementary experimental

               animal model in various stages of drug discovery and development, from disease modeling
               and target validation to drug safety, toxicology, and target screening. They are highly

               preferred by researchers due to their similarity to humans  in morphological, molecular,
               genetic, and pathological characteristics. Other advantages of zebrafish include their small

               size, easy and inexpensive care, a large genetic database, the absence of ethical restrictions

               in embryo testing, the optically clear appearance of embryos and larvae, which allows for
               high-throughput imaging-based phenotypic screening, and their high reproductive capacity.

                     The selectivity and efficacy of new drug molecules should be evaluated using different
               in vitro and  in vivo approaches, especially  in the preclinical phase. The robustness and

               precision of preclinical findings play a crucial role in the targeted conduct of clinical trials. To
               this  end, during the drug discovery process, many drugs are  examined for their ADME

               (absorption, distribution, metabolism, and excretion) properties using both in vitro and in vivo

               resources. Physiologically Based Pharmacokinetic Modeling (BPM), a frequently used
               pharmacokinetic model  in modern drug discovery and development,  is defined as
               mathematical modeling based on physiology. It combines information about a drug with

               independent prior knowledge of its physiology and biology at the organismal level to generate

               mechanistic representations of the drug, generating drug concentration-time profiles.
               Overall, zebrafish models provide an innovative bridge between in vitro systems and

               mammalian  studies, accelerating drug development while also improving safety, cost-
               effectiveness, and translational relevance.

               Keywords: Zebrafish, drug discovery, pharmacokinetics, PBPK modelling, ADME.




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