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Alleviating liver failure conditions using an integrated hybrid cryogel based cellular bioreactor as a bioartificial liver support

Conventionally, some bioartificial liver devices are used with separate plasmapheresis unit to separate out plasma from whole blood and adsorbent column to detoxify plasma before it passes through a hepatocytes-laden bioreactor. We aim to develop a hybrid bioreactor that integrates the separate modu...

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Autores principales: Damania, Apeksha, Hassan, Mohsin, Shirakigawa, Nana, Mizumoto, Hiroshi, Kumar, Anupam, Sarin, Shiv K., Ijima, Hiroyuki, Kamihira, Masamichi, Kumar, Ashok
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5227920/
https://www.ncbi.nlm.nih.gov/pubmed/28079174
http://dx.doi.org/10.1038/srep40323
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author Damania, Apeksha
Hassan, Mohsin
Shirakigawa, Nana
Mizumoto, Hiroshi
Kumar, Anupam
Sarin, Shiv K.
Ijima, Hiroyuki
Kamihira, Masamichi
Kumar, Ashok
author_facet Damania, Apeksha
Hassan, Mohsin
Shirakigawa, Nana
Mizumoto, Hiroshi
Kumar, Anupam
Sarin, Shiv K.
Ijima, Hiroyuki
Kamihira, Masamichi
Kumar, Ashok
author_sort Damania, Apeksha
collection PubMed
description Conventionally, some bioartificial liver devices are used with separate plasmapheresis unit to separate out plasma from whole blood and adsorbent column to detoxify plasma before it passes through a hepatocytes-laden bioreactor. We aim to develop a hybrid bioreactor that integrates the separate modules in one compact design improving the efficacy of the cryogel based bioreactor as a bioartificial liver support. A plasma separation membrane and an activated carbon cloth are placed over a HepG2-loaded cryogel scaffold in a three-chambered bioreactor design. This bioreactor is consequently connected extracorporeally to a rat model of acute liver failure for 3 h and major biochemical parameters studied. Bilirubin and aspartate transaminase showed a percentage decrease of 20–60% in the integrated bioreactor as opposed to 5–15% in the conventional setup. Urea and ammonia levels which showed negligible change in the conventional setup increase (40%) and decrease (18%), respectively in the integrated system. Also, an overall increase of 5% in human albumin in rat plasma indicated bioreactor functionality in terms of synthetic functions. These results were corroborated by offline evaluation of patient plasma. Hence, integrating the plasmapheresis and adsorbent units with the bioreactor module in one compact design improves the efficacy of the bioartificial liver device.
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spelling pubmed-52279202017-01-17 Alleviating liver failure conditions using an integrated hybrid cryogel based cellular bioreactor as a bioartificial liver support Damania, Apeksha Hassan, Mohsin Shirakigawa, Nana Mizumoto, Hiroshi Kumar, Anupam Sarin, Shiv K. Ijima, Hiroyuki Kamihira, Masamichi Kumar, Ashok Sci Rep Article Conventionally, some bioartificial liver devices are used with separate plasmapheresis unit to separate out plasma from whole blood and adsorbent column to detoxify plasma before it passes through a hepatocytes-laden bioreactor. We aim to develop a hybrid bioreactor that integrates the separate modules in one compact design improving the efficacy of the cryogel based bioreactor as a bioartificial liver support. A plasma separation membrane and an activated carbon cloth are placed over a HepG2-loaded cryogel scaffold in a three-chambered bioreactor design. This bioreactor is consequently connected extracorporeally to a rat model of acute liver failure for 3 h and major biochemical parameters studied. Bilirubin and aspartate transaminase showed a percentage decrease of 20–60% in the integrated bioreactor as opposed to 5–15% in the conventional setup. Urea and ammonia levels which showed negligible change in the conventional setup increase (40%) and decrease (18%), respectively in the integrated system. Also, an overall increase of 5% in human albumin in rat plasma indicated bioreactor functionality in terms of synthetic functions. These results were corroborated by offline evaluation of patient plasma. Hence, integrating the plasmapheresis and adsorbent units with the bioreactor module in one compact design improves the efficacy of the bioartificial liver device. Nature Publishing Group 2017-01-12 /pmc/articles/PMC5227920/ /pubmed/28079174 http://dx.doi.org/10.1038/srep40323 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Damania, Apeksha
Hassan, Mohsin
Shirakigawa, Nana
Mizumoto, Hiroshi
Kumar, Anupam
Sarin, Shiv K.
Ijima, Hiroyuki
Kamihira, Masamichi
Kumar, Ashok
Alleviating liver failure conditions using an integrated hybrid cryogel based cellular bioreactor as a bioartificial liver support
title Alleviating liver failure conditions using an integrated hybrid cryogel based cellular bioreactor as a bioartificial liver support
title_full Alleviating liver failure conditions using an integrated hybrid cryogel based cellular bioreactor as a bioartificial liver support
title_fullStr Alleviating liver failure conditions using an integrated hybrid cryogel based cellular bioreactor as a bioartificial liver support
title_full_unstemmed Alleviating liver failure conditions using an integrated hybrid cryogel based cellular bioreactor as a bioartificial liver support
title_short Alleviating liver failure conditions using an integrated hybrid cryogel based cellular bioreactor as a bioartificial liver support
title_sort alleviating liver failure conditions using an integrated hybrid cryogel based cellular bioreactor as a bioartificial liver support
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5227920/
https://www.ncbi.nlm.nih.gov/pubmed/28079174
http://dx.doi.org/10.1038/srep40323
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