Studying metabolism with multi-organ chips: new tools for disease modelling, pharmacokinetics and pharmacodynamics

Author:

Shroff Tanvi12ORCID,Aina Kehinde3,Maass Christian4ORCID,Cipriano Madalena2ORCID,Lambrecht Joeri5,Tacke Frank5ORCID,Mosig Alexander3ORCID,Loskill Peter126ORCID

Affiliation:

1. NMI Natural and Medical Sciences Institute at the University of Tübingen, Reutlingen, Germany

2. Department for Microphysiological Systems, Institute for Biomedical Engineering, Faculty of Medicine, Eberhard Karls University Tübingen, Österbergstraße 3, 72074 Tübingen, Germany

3. Institute of Biochemistry II, Center for Sepsis Control and Care, Jena University Hospital, Jena, Germany

4. esqLABS GmbH, Saterland, Germany

5. Department of Hepatology and Gastroenterology, Charité University Medicine Berlin, Campus Virchow Klinikum and Campus Charité Mitte, Berlin, Germany

6. 3R-Center for In vitro Models and Alternatives to Animal Testing, Eberhard Karls University Tübingen, Tübingen, Germany

Abstract

Non-clinical models to study metabolism including animal models and cell assays are often limited in terms of species translatability and predictability of human biology. This field urgently requires a push towards more physiologically accurate recapitulations of drug interactions and disease progression in the body. Organ-on-chip systems, specifically multi-organ chips (MOCs), are an emerging technology that is well suited to providing a species-specific platform to study the various types of metabolism (glucose, lipid, protein and drug) by recreating organ-level function. This review provides a resource for scientists aiming to study human metabolism by providing an overview of MOCs recapitulating aspects of metabolism, by addressing the technical aspects of MOC development and by providing guidelines for correlation with in silico models. The current state and challenges are presented for two application areas: (i) disease modelling and (ii) pharmacokinetics/pharmacodynamics. Additionally, the guidelines to integrate the MOC data into in silico models could strengthen the predictive power of the technology. Finally, the translational aspects of metabolizing MOCs are addressed, including adoption for personalized medicine and prospects for the clinic. Predictive MOCs could enable a significantly reduced dependence on animal models and open doors towards economical non-clinical testing and understanding of disease mechanisms.

Funder

European Commission

MSCA-IF-EF-ST - Standard EF to MC

MSCA-ITN-ETN-European Training Networks

Ministry of Science, Research and the Arts of Baden-Württemberg

CSA - Coordination and support action

Publisher

The Royal Society

Subject

General Biochemistry, Genetics and Molecular Biology,Immunology,General Neuroscience

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