| Literature DB >> 29029591 |
Lorna Ewart1, Eva-Maria Dehne2, Kristin Fabre3, Susan Gibbs4,5, James Hickman6, Ellinor Hornberg7, Magnus Ingelman-Sundberg8, Kyung-Jin Jang9, David R Jones10, Volker M Lauschke8, Uwe Marx2, Jerome T Mettetal3, Amy Pointon1, Dominic Williams1, Wolfram-Hubertus Zimmermann11,12, Peter Newham1.
Abstract
Enhancing the early detection of new therapies that are likely to carry a safety liability in the context of the intended patient population would provide a major advance in drug discovery. Microphysiological systems (MPS) technology offers an opportunity to support enhanced preclinical to clinical translation through the generation of higher-quality preclinical physiological data. In this review, we highlight this technological opportunity by focusing on key target organs associated with drug safety and metabolism. By focusing on MPS models that have been developed for these organs, alongside other relevant in vitro models, we review the current state of the art and the challenges that still need to be overcome to ensure application of this technology in enhancing drug discovery.Entities:
Keywords: drug discovery; microphysiological systems; toxicology
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Year: 2017 PMID: 29029591 DOI: 10.1146/annurev-pharmtox-010617-052722
Source DB: PubMed Journal: Annu Rev Pharmacol Toxicol ISSN: 0362-1642 Impact factor: 13.820