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Microphysiological systems in absorption, distribution, metabolism, and elimination sciences
The use of microphysiological systems (MPS) to support absorption, distribution, metabolism, and elimination (ADME) sciences has grown substantially in the last decade, in part driven by regulatory demands to move away from traditional animal‐based safety assessment studies and industry desires to d...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8742652/ https://www.ncbi.nlm.nih.gov/pubmed/34378335 http://dx.doi.org/10.1111/cts.13132 |
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author | Van Ness, Kirk P. Cesar, Francine Yeung, Catherine K. Himmelfarb, Jonathan Kelly, Edward J. |
author_facet | Van Ness, Kirk P. Cesar, Francine Yeung, Catherine K. Himmelfarb, Jonathan Kelly, Edward J. |
author_sort | Van Ness, Kirk P. |
collection | PubMed |
description | The use of microphysiological systems (MPS) to support absorption, distribution, metabolism, and elimination (ADME) sciences has grown substantially in the last decade, in part driven by regulatory demands to move away from traditional animal‐based safety assessment studies and industry desires to develop methodologies to efficiently screen and characterize drugs in the development pipeline. The past decade of MPS development has yielded great user‐driven technological advances with the collective fine‐tuning of cell culture techniques, fluid delivery systems, materials engineering, and performance enhancing modifications. The rapid advances in MPS technology have now made it feasible to evaluate critical ADME parameters within a stand‐alone organ system or through interconnected organ systems. This review surveys current MPS developed for liver, kidney, and intestinal systems as stand‐alone or interconnected organ systems, and evaluates each system for specific performance criteria recommended by regulatory authorities and MPS leaders that would render each system suitable for evaluating drug ADME. Whereas some systems are more suitable for ADME type research than others, not all system designs were intended to meet the recently published desired performance criteria and are reported as a summary of initial proof‐of‐concept studies. |
format | Online Article Text |
id | pubmed-8742652 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-87426522022-01-12 Microphysiological systems in absorption, distribution, metabolism, and elimination sciences Van Ness, Kirk P. Cesar, Francine Yeung, Catherine K. Himmelfarb, Jonathan Kelly, Edward J. Clin Transl Sci Reviews The use of microphysiological systems (MPS) to support absorption, distribution, metabolism, and elimination (ADME) sciences has grown substantially in the last decade, in part driven by regulatory demands to move away from traditional animal‐based safety assessment studies and industry desires to develop methodologies to efficiently screen and characterize drugs in the development pipeline. The past decade of MPS development has yielded great user‐driven technological advances with the collective fine‐tuning of cell culture techniques, fluid delivery systems, materials engineering, and performance enhancing modifications. The rapid advances in MPS technology have now made it feasible to evaluate critical ADME parameters within a stand‐alone organ system or through interconnected organ systems. This review surveys current MPS developed for liver, kidney, and intestinal systems as stand‐alone or interconnected organ systems, and evaluates each system for specific performance criteria recommended by regulatory authorities and MPS leaders that would render each system suitable for evaluating drug ADME. Whereas some systems are more suitable for ADME type research than others, not all system designs were intended to meet the recently published desired performance criteria and are reported as a summary of initial proof‐of‐concept studies. John Wiley and Sons Inc. 2021-08-26 2022-01 /pmc/articles/PMC8742652/ /pubmed/34378335 http://dx.doi.org/10.1111/cts.13132 Text en © 2021 The Authors. Clinical and Translational Science published by Wiley Periodicals LLC on behalf of American Society for Clinical Pharmacology and Therapeutics. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Reviews Van Ness, Kirk P. Cesar, Francine Yeung, Catherine K. Himmelfarb, Jonathan Kelly, Edward J. Microphysiological systems in absorption, distribution, metabolism, and elimination sciences |
title | Microphysiological systems in absorption, distribution, metabolism, and elimination sciences |
title_full | Microphysiological systems in absorption, distribution, metabolism, and elimination sciences |
title_fullStr | Microphysiological systems in absorption, distribution, metabolism, and elimination sciences |
title_full_unstemmed | Microphysiological systems in absorption, distribution, metabolism, and elimination sciences |
title_short | Microphysiological systems in absorption, distribution, metabolism, and elimination sciences |
title_sort | microphysiological systems in absorption, distribution, metabolism, and elimination sciences |
topic | Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8742652/ https://www.ncbi.nlm.nih.gov/pubmed/34378335 http://dx.doi.org/10.1111/cts.13132 |
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