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dc.rights.licenseCC-BY-NC-ND
dc.contributor.advisorExterne beoordelaar - External assesor,
dc.contributor.authorYilmaz, Habibe
dc.date.accessioned2023-07-01T00:00:43Z
dc.date.available2023-07-01T00:00:43Z
dc.date.issued2023
dc.identifier.urihttps://studenttheses.uu.nl/handle/20.500.12932/44073
dc.description.abstractIntroduction: The goal of this study was to develop a whole body physiological based pharmacokinetic-model (PBPK-model) to predict the tissue distribution of 18F-DCFPyL in patients with prostate cancer (PCa). Method: The model was extended from a previously published PBPK-model describing PCa patients to predict the tissue distribution of 18F-DCFPyL. This model describes the tumors and organs at risks. The model was simulated and the results were compared to literature observations of patients with metastatic PCa. Results: Our model adequately predicted the distribution of 18F-DCFPyL. Sensitivity analysis showed that the receptor densities, tumor flow and haematocrit had significant influence on the model outcome. The release and degradation of 18F-DCFPyL, and total organ volumes showed no significant influence on the outcome. Discussion: The tumor flow, receptor densities and haematocrit should be measured in the future to accurately predict tissue distribution. The release and degradation of 18F-DCFPyL, and total organ volumes can be fixed on literature data. Conclusion: The final PBPK-model was able to adequately predict tissue distribution of 18F-DCFPyL.
dc.description.sponsorshipUtrecht University
dc.language.isoEN
dc.subjectHet doel was om de weefselverdeling van 18F-DCFPyL in patiënten met prostaatkanker te voorspellen met behulp van een PBPK-model. 18F-DCFPyL is een PSMA-ligand en wordt momenteel gebruikt als tracer voor prostaatkanker.
dc.titlePHYSIOLOGICALY BASED PHARMACOKINTEIC MODELLING OF 18F-DCFPYL TO PREDICT THE TISSUE DISTRIBUTION IN PATIENTS WITH PROSTATE CANCER
dc.type.contentMaster Thesis
dc.rights.accessrightsOpen Access
dc.subject.keywordsPBPK-model; PSMA; Prostaatkanker; 18F-DCFPyL; Theranostics
dc.subject.courseuuFarmacie
dc.thesis.id10217


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