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Water-Permeable Dialysis Membranes for Multi-Layered Microdialysis System

This paper presents the development of water-permeable dialysis membranes that are suitable for an implantable microdialysis system that does not use dialysis fluid. We developed a microdialysis system integrating microfluidic channels and nanoporous filtering membranes made of polyethersulfone (PES...

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Detalles Bibliográficos
Autores principales: To, Naoya, Sanada, Ippei, Ito, Hikaru, Prihandana, Gunawan S., Morita, Shinya, Kanno, Yoshihiko, Miki, Norihisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4451643/
https://www.ncbi.nlm.nih.gov/pubmed/26082924
http://dx.doi.org/10.3389/fbioe.2015.00070
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author To, Naoya
Sanada, Ippei
Ito, Hikaru
Prihandana, Gunawan S.
Morita, Shinya
Kanno, Yoshihiko
Miki, Norihisa
author_facet To, Naoya
Sanada, Ippei
Ito, Hikaru
Prihandana, Gunawan S.
Morita, Shinya
Kanno, Yoshihiko
Miki, Norihisa
author_sort To, Naoya
collection PubMed
description This paper presents the development of water-permeable dialysis membranes that are suitable for an implantable microdialysis system that does not use dialysis fluid. We developed a microdialysis system integrating microfluidic channels and nanoporous filtering membranes made of polyethersulfone (PES), aiming at a fully implantable system that drastically improves the quality of life of patients. Simplicity of the total system is crucial for the implantable dialysis system, where the pumps and storage tanks for the dialysis fluid pose problems. Hence, we focus on hemofiltration, which does not require the dialysis fluid but water-permeable membranes. We investigated the water permeability of the PES membrane with respect to the concentrations of the PES, the additives, and the solvents in the casting solution. Sufficiently, water-permeable membranes were found through in vitro experiments using whole bovine blood. The filtrate was verified to have the concentrations of low-molecular-weight molecules, such as sodium, potassium, urea, and creatinine, while proteins, such as albumin, were successfully blocked by the membrane. We conducted in vivo experiments using rats, where the system was connected to the femoral artery and jugular vein. The filtrate was successfully collected without any leakage of blood inside the system and it did not contain albumin but low-molecular-weight molecules whose concentrations were identical to those of the blood. The rat model with renal failure showed 100% increase of creatinine in 5 h, while rats connected to the system showed only a 7.4% increase, which verified the effectiveness of the proposed microdialysis system.
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spelling pubmed-44516432015-06-16 Water-Permeable Dialysis Membranes for Multi-Layered Microdialysis System To, Naoya Sanada, Ippei Ito, Hikaru Prihandana, Gunawan S. Morita, Shinya Kanno, Yoshihiko Miki, Norihisa Front Bioeng Biotechnol Bioengineering and Biotechnology This paper presents the development of water-permeable dialysis membranes that are suitable for an implantable microdialysis system that does not use dialysis fluid. We developed a microdialysis system integrating microfluidic channels and nanoporous filtering membranes made of polyethersulfone (PES), aiming at a fully implantable system that drastically improves the quality of life of patients. Simplicity of the total system is crucial for the implantable dialysis system, where the pumps and storage tanks for the dialysis fluid pose problems. Hence, we focus on hemofiltration, which does not require the dialysis fluid but water-permeable membranes. We investigated the water permeability of the PES membrane with respect to the concentrations of the PES, the additives, and the solvents in the casting solution. Sufficiently, water-permeable membranes were found through in vitro experiments using whole bovine blood. The filtrate was verified to have the concentrations of low-molecular-weight molecules, such as sodium, potassium, urea, and creatinine, while proteins, such as albumin, were successfully blocked by the membrane. We conducted in vivo experiments using rats, where the system was connected to the femoral artery and jugular vein. The filtrate was successfully collected without any leakage of blood inside the system and it did not contain albumin but low-molecular-weight molecules whose concentrations were identical to those of the blood. The rat model with renal failure showed 100% increase of creatinine in 5 h, while rats connected to the system showed only a 7.4% increase, which verified the effectiveness of the proposed microdialysis system. Frontiers Media S.A. 2015-06-02 /pmc/articles/PMC4451643/ /pubmed/26082924 http://dx.doi.org/10.3389/fbioe.2015.00070 Text en Copyright © 2015 To, Sanada, Ito, Prihandana, Morita, Kanno and Miki. http://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) or licensor 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 Bioengineering and Biotechnology
To, Naoya
Sanada, Ippei
Ito, Hikaru
Prihandana, Gunawan S.
Morita, Shinya
Kanno, Yoshihiko
Miki, Norihisa
Water-Permeable Dialysis Membranes for Multi-Layered Microdialysis System
title Water-Permeable Dialysis Membranes for Multi-Layered Microdialysis System
title_full Water-Permeable Dialysis Membranes for Multi-Layered Microdialysis System
title_fullStr Water-Permeable Dialysis Membranes for Multi-Layered Microdialysis System
title_full_unstemmed Water-Permeable Dialysis Membranes for Multi-Layered Microdialysis System
title_short Water-Permeable Dialysis Membranes for Multi-Layered Microdialysis System
title_sort water-permeable dialysis membranes for multi-layered microdialysis system
topic Bioengineering and Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4451643/
https://www.ncbi.nlm.nih.gov/pubmed/26082924
http://dx.doi.org/10.3389/fbioe.2015.00070
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