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Application of In Vitro Metabolism Activation in High-Throughput Screening

In vitro methods which incorporate metabolic capability into the assays allow us to assess the activity of metabolites from their parent compounds. These methods can be applied into high-throughput screening (HTS) platforms, thereby increasing the speed to identify compounds that become active via t...

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Autores principales: Ooka, Masato, Lynch, Caitlin, Xia, Menghang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7663506/
https://www.ncbi.nlm.nih.gov/pubmed/33142951
http://dx.doi.org/10.3390/ijms21218182
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author Ooka, Masato
Lynch, Caitlin
Xia, Menghang
author_facet Ooka, Masato
Lynch, Caitlin
Xia, Menghang
author_sort Ooka, Masato
collection PubMed
description In vitro methods which incorporate metabolic capability into the assays allow us to assess the activity of metabolites from their parent compounds. These methods can be applied into high-throughput screening (HTS) platforms, thereby increasing the speed to identify compounds that become active via the metabolism process. HTS was originally used in the pharmaceutical industry and now is also used in academic settings to evaluate biological activity and/or toxicity of chemicals. Although most chemicals are metabolized in our body, many HTS assays lack the capability to determine compound activity via metabolism. To overcome this problem, several in vitro metabolic methods have been applied to an HTS format. In this review, we describe in vitro metabolism methods and their application in HTS assays, as well as discuss the future perspectives of HTS with metabolic activity. Each in vitro metabolism method has advantages and disadvantages. For instance, the S9 mix has a full set of liver metabolic enzymes, but it displays high cytotoxicity in cell-based assays. In vitro metabolism requires liver fractions or the use of other metabolically capable systems, including primary hepatocytes or recombinant enzymes. Several newly developed in vitro metabolic methods, including HepaRG cells, three-dimensional (3D) cell models, and organ-on-a-chip technology, will also be discussed. These newly developed in vitro metabolism approaches offer significant progress in dissecting biological processes, developing drugs, and making toxicology studies quicker and more efficient.
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spelling pubmed-76635062020-11-14 Application of In Vitro Metabolism Activation in High-Throughput Screening Ooka, Masato Lynch, Caitlin Xia, Menghang Int J Mol Sci Review In vitro methods which incorporate metabolic capability into the assays allow us to assess the activity of metabolites from their parent compounds. These methods can be applied into high-throughput screening (HTS) platforms, thereby increasing the speed to identify compounds that become active via the metabolism process. HTS was originally used in the pharmaceutical industry and now is also used in academic settings to evaluate biological activity and/or toxicity of chemicals. Although most chemicals are metabolized in our body, many HTS assays lack the capability to determine compound activity via metabolism. To overcome this problem, several in vitro metabolic methods have been applied to an HTS format. In this review, we describe in vitro metabolism methods and their application in HTS assays, as well as discuss the future perspectives of HTS with metabolic activity. Each in vitro metabolism method has advantages and disadvantages. For instance, the S9 mix has a full set of liver metabolic enzymes, but it displays high cytotoxicity in cell-based assays. In vitro metabolism requires liver fractions or the use of other metabolically capable systems, including primary hepatocytes or recombinant enzymes. Several newly developed in vitro metabolic methods, including HepaRG cells, three-dimensional (3D) cell models, and organ-on-a-chip technology, will also be discussed. These newly developed in vitro metabolism approaches offer significant progress in dissecting biological processes, developing drugs, and making toxicology studies quicker and more efficient. MDPI 2020-10-31 /pmc/articles/PMC7663506/ /pubmed/33142951 http://dx.doi.org/10.3390/ijms21218182 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Ooka, Masato
Lynch, Caitlin
Xia, Menghang
Application of In Vitro Metabolism Activation in High-Throughput Screening
title Application of In Vitro Metabolism Activation in High-Throughput Screening
title_full Application of In Vitro Metabolism Activation in High-Throughput Screening
title_fullStr Application of In Vitro Metabolism Activation in High-Throughput Screening
title_full_unstemmed Application of In Vitro Metabolism Activation in High-Throughput Screening
title_short Application of In Vitro Metabolism Activation in High-Throughput Screening
title_sort application of in vitro metabolism activation in high-throughput screening
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7663506/
https://www.ncbi.nlm.nih.gov/pubmed/33142951
http://dx.doi.org/10.3390/ijms21218182
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