Cited by 593D Printing in Biomedical ResearchTissue Engineering and Regenerative MedicineMicrofluidic and Capillary Electrophoresis Applications

Self-contained, low-cost Body-on-a-Chip systems for drug development

Open access
Wang, Ying I, Oleaga, Carlota, Long, Christopher J, Esch, Mandy B, McAleer, Christopher W, Miller, Paula G, Hickman, James J, Shuler, Michael L·2017·Experimental Biology and Medicine

Abstract

Integrated multi-organ microphysiological systems are an evolving tool for preclinical evaluation of the potential toxicity and efficacy of drug candidates. Such systems, also known as Body-on-a-Chip devices, have a great potential to increase the successful conversion of drug candidates entering clinical trials into approved drugs. Systems, to be attractive for commercial adoption, need to be inexpensive, easy to operate, and give reproducible results. Further, the ability to measure functional responses, such as electrical activity, force generation, and barrier integrity of organ surrogates, enhances the ability to monitor response to drugs. The ability to operate a system for significant periods of time (up to 28 d) will provide potential to estimate chronic as well as acute responses of the human body. Here we review progress towards a self-contained low-cost microphysiological system with functional measurements of physiological responses. Impact statement: Multi-organ microphysiological systems are promising devices to improve the drug development process. The development of a pumpless system represents the ability to build multi-organ systems that are of low cost, high reliability, and self-contained. These features, coupled with the ability to measure electrical and mechanical response in addition to chemical or metabolic changes, provides an attractive system for incorporation into the drug development process. This will be the most complete review of the pumpless platform with recirculation yet written.

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Crossref · 10.1177/1535370217694101

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  • Microfluidic systems can link different organs-on-a-chip to potentially simulate the complexity of multiorgan drug metabolism and pharmacokinetics.

    “Furthermore, microfluidic systems can link different organs-on-a-chip to potentially simulate the complexity of multiorgan drug metabolism and pharmacokinetics9,47,50,68–71.”

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References 91 · Cited by 59

Authors
Wang, Y. I., Oleaga, C., Long, C. J., Esch, M. B., McAleer, C. W., Miller, P. G., Hickman, J. J., & Shuler, M. L.
Affiliations
  • Cornell University (US)
  • University of Central Florida (US)
  • National Institute of Standards and Technology (US)
Corresponding author
Shuler, Michael L
Venue
Experimental Biology and Medicine
Published
2017-02-17
Volume
242
Issue
17
Pages
1701-1713
ISSN
  • 0071-3384 (ISSN-L)
  • 1535-3702
  • 1535-3699
OpenAlex
W2588617183
Cited by
59
References
91
Citations by year
2026: 2 · 2025: 3 · 2024: 6 · 2023: 5 · 2022: 4 · 2021: 10 · 2020: 9 · 2019: 8 · 2018: 9 · 2017: 3
FWCI
3.57
Type
journal article
Language
en
Open access
Locations
  • Experimental Biology and Medicine (publishedVersion)
  • Europe PMC (PubMed Central) (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
  • Journal of International Crisis and Risk Communication Research (submittedVersion)
Funders
  • National Institutes of Health (R44TR001326, UH2TR000516)
  • National Center for Advancing Translational Sciences (R44 TR001326-0A1)
Topics
  • Physical Sciences › Engineering › Biomedical Engineering › 3D Printing in Biomedical Research
  • Health Sciences › Medicine › Surgery › Tissue Engineering and Regenerative Medicine
  • Physical Sciences › Engineering › Biomedical Engineering › Microfluidic and Capillary Electrophoresis Applications
Keywords
body-on-a-chip, drug development, drug toxicity assessment, electrical activity, barrier integrity
MeSH terms
Drug Evaluation, Preclinical, Humans, Models, Biological, Cell Culture Techniques, Microchip Analytical Procedures, Lab-On-A-Chip Devices

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