Microphysiological Systems Evaluation: Experience of TEX-VAL Tissue Chip Testing Consortium

Author:

Rusyn Ivan1,Sakolish Courtney1,Kato Yuki1,Stephan Clifford2,Vergara Leoncio2,Hewitt Philip3ORCID,Bhaskaran Vasanthi4,Davis Myrtle4,Hardwick Rhiannon N5ORCID,Ferguson Stephen S6ORCID,Stanko Jason P6,Bajaj Piyush7,Adkins Karissa7,Sipes Nisha S8,Hunter E Sidney8,Baltazar Maria T9,Carmichael Paul L9,Sadh Kritika9,Becker Richard A10

Affiliation:

1. Department of Veterinary Physiology and Pharmacology, Texas A&M University , College Station, Texas 77843, USA

2. Institute of Biosciences and Technology, Texas A&M University , Houston, Texas 77030, USA

3. Chemical and Preclinical Safety, Merck Healthcare KGaA , Darmstadt, Germany

4. Discovery Toxicology, Bristol Myers Squibb , Princeton, New Jersey 08543, USA

5. Discovery Toxicology, Bristol Myers Squibb , San Diego, California 92130, USA

6. Division of the National Toxicology Program, National Institute of Environmental Health Sciences, Research Triangle Park , North Carolina 27709, USA

7. Global Investigative Toxicology, Preclinical Safety, Sanofi , Framingham, Massachusetts 01701, USA

8. Center for Computational Toxicology and Exposure, Office of Research and Development, U.S. Environmental Protection Agency , Research Triangle Park, North Carolina, 27711, USA

9. Unilever Safety and Environmental Assurance Centre , Bedfordshire, Sharnbrook MK44 1LQ, UK

10. American Chemistry Council , Washington, District of Columbia 20002, USA

Abstract

Abstract Much has been written and said about the promise and excitement of microphysiological systems, miniature devices that aim to recreate aspects of human physiology on a chip. The rapid explosion of the offerings and persistent publicity placed high expectations on both product manufacturers and regulatory agencies to adopt the data. Inevitably, discussions of where this technology fits in chemical testing paradigms are ongoing. Some end-users became early adopters, whereas others have taken a more cautious approach because of the high cost and uncertainties of their utility. Here, we detail the experience of a public-private collaboration established for testing of diverse microphysiological systems. Collectively, we present a number of considerations on practical aspects of using microphysiological systems in the context of their applications in decision-making. Specifically, future end-users need to be prepared for extensive on-site optimization and have access to a wide range of imaging and other equipment. We reason that cells, related reagents, and the technical skills of the research staff, not the devices themselves, are the most critical determinants of success. Extrapolation from concentration-response effects in microphysiological systems to human blood or oral exposures, difficulties with replicating the whole organ, and long-term functionality remain as critical challenges. Overall, we conclude that it is unlikely that a rodent- or human-equivalent model is achievable through a finite number of microphysiological systems in the near future; therefore, building consensus and promoting the gradual incorporation of these models into tiered approaches for safety assessment and decision-making is the sensible path to wide adoption.

Funder

National Center for Advancing Translational Sciences

Publisher

Oxford University Press (OUP)

Subject

Toxicology

Reference73 articles.

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