Latest impact of engineered human liver platforms on drug development
Drug-induced liver injury (DILI) is a leading cause of drug attrition, which is partly due to differences between preclinical animals and humans in metabolic pathways. Therefore, in vitro human liver models are utilized in biopharmaceutical practice to mitigate DILI risk and assess related mechanism...
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2021-09-01
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Online Access: | http://dx.doi.org/10.1063/5.0051765 |
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doaj-29bbb9b6946e43d7b5e9253b38136a9a2021-10-06T14:17:39ZengAIP Publishing LLCAPL Bioengineering2473-28772021-09-0153031506031506-1710.1063/5.0051765Latest impact of engineered human liver platforms on drug developmentChase P. Monckton0Grace E. Brown1Salman R. Khetani2Department of Bioengineering, University of Illinois at Chicago, Chicago, Illinois 60607, USADepartment of Bioengineering, University of Illinois at Chicago, Chicago, Illinois 60607, USADepartment of Bioengineering, University of Illinois at Chicago, Chicago, Illinois 60607, USADrug-induced liver injury (DILI) is a leading cause of drug attrition, which is partly due to differences between preclinical animals and humans in metabolic pathways. Therefore, in vitro human liver models are utilized in biopharmaceutical practice to mitigate DILI risk and assess related mechanisms of drug transport and metabolism. However, liver cells lose phenotypic functions within 1–3 days in two-dimensional monocultures on collagen-coated polystyrene/glass, which precludes their use to model the chronic effects of drugs and disease stimuli. To mitigate such a limitation, bioengineers have adapted tools from the semiconductor industry and additive manufacturing to precisely control the microenvironment of liver cells. Such tools have led to the fabrication of advanced two-dimensional and three-dimensional human liver platforms for different throughput needs and assay endpoints (e.g., micropatterned cocultures, spheroids, organoids, bioprinted tissues, and microfluidic devices); such platforms have significantly enhanced liver functions closer to physiologic levels and improved functional lifetime to >4 weeks, which has translated to higher sensitivity for predicting drug outcomes and enabling modeling of diseased phenotypes for novel drug discovery. Here, we focus on commercialized engineered liver platforms and case studies from the biopharmaceutical industry showcasing their impact on drug development. We also discuss emerging multi-organ microfluidic devices containing a liver compartment that allow modeling of inter-tissue crosstalk following drug exposure. Finally, we end with key requirements for engineered liver platforms to become routine fixtures in the biopharmaceutical industry toward reducing animal usage and providing patients with safe and efficacious drugs with unprecedented speed and reduced cost.http://dx.doi.org/10.1063/5.0051765 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Chase P. Monckton Grace E. Brown Salman R. Khetani |
spellingShingle |
Chase P. Monckton Grace E. Brown Salman R. Khetani Latest impact of engineered human liver platforms on drug development APL Bioengineering |
author_facet |
Chase P. Monckton Grace E. Brown Salman R. Khetani |
author_sort |
Chase P. Monckton |
title |
Latest impact of engineered human liver platforms on drug development |
title_short |
Latest impact of engineered human liver platforms on drug development |
title_full |
Latest impact of engineered human liver platforms on drug development |
title_fullStr |
Latest impact of engineered human liver platforms on drug development |
title_full_unstemmed |
Latest impact of engineered human liver platforms on drug development |
title_sort |
latest impact of engineered human liver platforms on drug development |
publisher |
AIP Publishing LLC |
series |
APL Bioengineering |
issn |
2473-2877 |
publishDate |
2021-09-01 |
description |
Drug-induced liver injury (DILI) is a leading cause of drug attrition, which is partly due to differences between preclinical animals and humans in metabolic pathways. Therefore, in vitro human liver models are utilized in biopharmaceutical practice to mitigate DILI risk and assess related mechanisms of drug transport and metabolism. However, liver cells lose phenotypic functions within 1–3 days in two-dimensional monocultures on collagen-coated polystyrene/glass, which precludes their use to model the chronic effects of drugs and disease stimuli. To mitigate such a limitation, bioengineers have adapted tools from the semiconductor industry and additive manufacturing to precisely control the microenvironment of liver cells. Such tools have led to the fabrication of advanced two-dimensional and three-dimensional human liver platforms for different throughput needs and assay endpoints (e.g., micropatterned cocultures, spheroids, organoids, bioprinted tissues, and microfluidic devices); such platforms have significantly enhanced liver functions closer to physiologic levels and improved functional lifetime to >4 weeks, which has translated to higher sensitivity for predicting drug outcomes and enabling modeling of diseased phenotypes for novel drug discovery. Here, we focus on commercialized engineered liver platforms and case studies from the biopharmaceutical industry showcasing their impact on drug development. We also discuss emerging multi-organ microfluidic devices containing a liver compartment that allow modeling of inter-tissue crosstalk following drug exposure. Finally, we end with key requirements for engineered liver platforms to become routine fixtures in the biopharmaceutical industry toward reducing animal usage and providing patients with safe and efficacious drugs with unprecedented speed and reduced cost. |
url |
http://dx.doi.org/10.1063/5.0051765 |
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