AI Article Synopsis

  • Physiologically based pharmacokinetic (PBPK) and population pharmacokinetic (PK) modeling are established in drug research but have limited application in radiopharmaceutical development.
  • A literature review examined studies using PBPK and population PK modeling specifically for radiopharmaceuticals, identifying 28 relevant articles that demonstrated added value in predictive modeling and understanding individual variations.
  • The findings suggest that further implementation of PK modeling in radiopharmaceuticals could enhance treatment planning, optimize dosing, and improve knowledge of inter-patient differences and drug interactions.

Article Abstract

Physiologically based pharmacokinetic (PBPK) and population pharmacokinetic (PK) modelling approaches are widely accepted in non-radiopharmaceutical drug development and research, while there is no major role for these approaches in radiopharmaceutical development yet. In this review, a literature search was performed to specify different research purposes and questions that have previously been answered using both PBPK and population PK modelling for radiopharmaceuticals. The literature search was performed using the databases PubMed and Embase. Wide search terms included radiopharmaceutical, tracer, radioactivity, physiologically based pharmacokinetic model, PBPK, population pharmacokinetic model and nonlinear mixed-effects model. Eight articles and twenty articles were included for this review based on this literature search for population PK modelling and PBPK modelling, respectively. Included population PK analyses showed to have an added value to develop predictive models for a population and to describe individual variability sources. Main purposes of PBPK models appeared related to optimizing treatment (planning), or more specifically: to find the optimal combination of peptide amount and radioactivity, to optimize treatment planning by reducing the number of measurements, to individualize treatment, to get insights in differences between pre-therapeutic and therapeutic scans or to understand inter-patient differences. Other main research subjects were regarding radiopharmaceutical comparisons, selecting ligands based on their peptide characteristics and gaining a better understanding of drug-drug interactions. The use of PK modelling approaches in radiopharmaceutical research remains scarce, but can be expanded to obtain a better understanding of PK and whole-body distribution of radiopharmaceuticals in general. PK modelling of radiopharmaceuticals has great potential for the nearby future and could contribute to the evolving research of radiopharmaceuticals.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9706588PMC
http://dx.doi.org/10.7150/thno.77279DOI Listing

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