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Prospect of in vitro Bile Fluids Collection in Improving Cell-Based Assay of Liver Function
The liver plays a pivotal role in the clearance of drugs. Reliable assays for liver function are crucial for various metabolism investigation, including toxicity, disease, and pre-clinical testing for drug development. Bile is an aqueous secretion of a functioning liver. Analyses of bile are used to...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8915818/ https://www.ncbi.nlm.nih.gov/pubmed/35295147 http://dx.doi.org/10.3389/ftox.2021.657432 |
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author | Rizki-Safitri, Astia Tokito, Fumiya Nishikawa, Masaki Tanaka, Minoru Maeda, Kazuya Kusuhara, Hiroyuki Sakai, Yasuyuki |
author_facet | Rizki-Safitri, Astia Tokito, Fumiya Nishikawa, Masaki Tanaka, Minoru Maeda, Kazuya Kusuhara, Hiroyuki Sakai, Yasuyuki |
author_sort | Rizki-Safitri, Astia |
collection | PubMed |
description | The liver plays a pivotal role in the clearance of drugs. Reliable assays for liver function are crucial for various metabolism investigation, including toxicity, disease, and pre-clinical testing for drug development. Bile is an aqueous secretion of a functioning liver. Analyses of bile are used to explain drug clearance and related effects and are thus important for toxicology and pharmacokinetic research. Bile fluids collection is extensively performed in vivo, whereas this process is rarely reproduced as in the in vitro studies. The key to success is the technology involved, which needs to satisfy multiple criteria. To ensure the accuracy of subsequent chemical analyses, certain amounts of bile are needed. Additionally, non-invasive and continuous collections are preferable in view of cell culture. In this review, we summarize recent progress and limitations in the field. We highlight attempts to develop advanced liver cultures for bile fluids collection, including methods to stimulate the secretion of bile in vitro. With these strategies, researchers have used a variety of cell sources, extracellular matrix proteins, and growth factors to investigate different cell-culture environments, including three-dimensional spheroids, cocultures, and microfluidic devices. Effective combinations of expertise and technology have the potential to overcome these obstacles to achieve reliable in vitro bile assay systems. |
format | Online Article Text |
id | pubmed-8915818 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-89158182022-03-15 Prospect of in vitro Bile Fluids Collection in Improving Cell-Based Assay of Liver Function Rizki-Safitri, Astia Tokito, Fumiya Nishikawa, Masaki Tanaka, Minoru Maeda, Kazuya Kusuhara, Hiroyuki Sakai, Yasuyuki Front Toxicol Toxicology The liver plays a pivotal role in the clearance of drugs. Reliable assays for liver function are crucial for various metabolism investigation, including toxicity, disease, and pre-clinical testing for drug development. Bile is an aqueous secretion of a functioning liver. Analyses of bile are used to explain drug clearance and related effects and are thus important for toxicology and pharmacokinetic research. Bile fluids collection is extensively performed in vivo, whereas this process is rarely reproduced as in the in vitro studies. The key to success is the technology involved, which needs to satisfy multiple criteria. To ensure the accuracy of subsequent chemical analyses, certain amounts of bile are needed. Additionally, non-invasive and continuous collections are preferable in view of cell culture. In this review, we summarize recent progress and limitations in the field. We highlight attempts to develop advanced liver cultures for bile fluids collection, including methods to stimulate the secretion of bile in vitro. With these strategies, researchers have used a variety of cell sources, extracellular matrix proteins, and growth factors to investigate different cell-culture environments, including three-dimensional spheroids, cocultures, and microfluidic devices. Effective combinations of expertise and technology have the potential to overcome these obstacles to achieve reliable in vitro bile assay systems. Frontiers Media S.A. 2021-06-03 /pmc/articles/PMC8915818/ /pubmed/35295147 http://dx.doi.org/10.3389/ftox.2021.657432 Text en Copyright © 2021 Rizki-Safitri, Tokito, Nishikawa, Tanaka, Maeda, Kusuhara and Sakai. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Toxicology Rizki-Safitri, Astia Tokito, Fumiya Nishikawa, Masaki Tanaka, Minoru Maeda, Kazuya Kusuhara, Hiroyuki Sakai, Yasuyuki Prospect of in vitro Bile Fluids Collection in Improving Cell-Based Assay of Liver Function |
title | Prospect of in vitro Bile Fluids Collection in Improving Cell-Based Assay of Liver Function |
title_full | Prospect of in vitro Bile Fluids Collection in Improving Cell-Based Assay of Liver Function |
title_fullStr | Prospect of in vitro Bile Fluids Collection in Improving Cell-Based Assay of Liver Function |
title_full_unstemmed | Prospect of in vitro Bile Fluids Collection in Improving Cell-Based Assay of Liver Function |
title_short | Prospect of in vitro Bile Fluids Collection in Improving Cell-Based Assay of Liver Function |
title_sort | prospect of in vitro bile fluids collection in improving cell-based assay of liver function |
topic | Toxicology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8915818/ https://www.ncbi.nlm.nih.gov/pubmed/35295147 http://dx.doi.org/10.3389/ftox.2021.657432 |
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