Extension of the Virtual Cell Based Assay from a 2-D to a 3-D Cell Culture Model

Ewa Bednarczyk, Yanfei Lu, Alicia Paini, Sofia Batista Leite, Leo A van Grunsven, Andrew Worth, Maurice Whelan

Research output: Contribution to journalArticlepeer-review

3 Citations (Scopus)
37 Downloads (Pure)

Abstract

Prediction of chemical toxicity is very useful in risk assessment. With the current paradigm shift towards the use of in vitro and in silico systems, we present herein a theoretical mathematical description of a quasi-diffusion process to predict chemical concentrations in 3-D spheroid cell cultures. By extending a 2-D Virtual Cell Based Assay (VCBA) model into a 3-D spheroid cell model, we assume that cells are arranged in a series of concentric layers within the sphere. We formulate the chemical quasi-diffusion process by simplifying the spheroid with respect to the number of cells in each layer. The system was calibrated and tested with acetaminophen (APAP). Simulated predictions of APAP toxicity were compared with empirical data from in vitro measurements by using a 3-D spheroid model. The results of this first attempt to extend the VCBA model are promising - they show that the VCBA model simulates close correlation between the influence of compound concentration and the viability of the HepaRG 3-D cell culture. The 3-D VCBA model provides a complement to current in vitro procedures to refine experimental setups, to fill data gaps and help in the interpretation of in vitro data for the purposes of risk assessment.

Original languageEnglish
Pages (from-to)45-56
Number of pages12
JournalATLA. Alternatives to Laboratory Animals
Volume50
Issue number1
Early online date2022
DOIs
Publication statusPublished - Jan 2022

Bibliographical note

Funding Information:
The authors would like to acknowledge Professor Tomasz Lekszycki for his support in reviewing the draft of this paper. The author(s) received no financial support for the research, authorship, and/or publication of this article.

Publisher Copyright:
© The Author(s) 2022.

Copyright:
Copyright 2022 Elsevier B.V., All rights reserved.

Keywords

  • HepaRG
  • chemical exposure
  • distribution model
  • fate modelling
  • in silico
  • in vitro
  • mathematical modelling
  • multiscale cell culture
  • spheroids

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