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Study of Uremic Toxin Fluxes Across Nanofabricated Hemodialysis Membranes Using Irreversible Thermodynamics

INTRODUCTION: The flux of uremic toxin middle molecules through currently used hemodialysis membranes is suboptimal, mainly because of the membranes’ pore architecture. AIM: Identifying the modifiable sieving parameters that can be improved by nanotechnology to enhance fluxes of uremic toxins across...

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Autores principales: Hedayat, Assem, Peace, Rob, Elmoselhi, Hamdi, Shoker, Ahmed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Research Network of Computational and Structural Biotechnology (RNCSB) Organization 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3962091/
https://www.ncbi.nlm.nih.gov/pubmed/24688713
http://dx.doi.org/10.5936/csbj.201303005
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author Hedayat, Assem
Peace, Rob
Elmoselhi, Hamdi
Shoker, Ahmed
author_facet Hedayat, Assem
Peace, Rob
Elmoselhi, Hamdi
Shoker, Ahmed
author_sort Hedayat, Assem
collection PubMed
description INTRODUCTION: The flux of uremic toxin middle molecules through currently used hemodialysis membranes is suboptimal, mainly because of the membranes’ pore architecture. AIM: Identifying the modifiable sieving parameters that can be improved by nanotechnology to enhance fluxes of uremic toxins across the walls of dialyzers’ capillaries. METHODS: We determined the maximal dimensions of endothelin, cystatin C, and interleukin – 6 using the macromolecular modeling software, COOT. We also applied the expanded Nernst-Plank equation to calculate the changes in the overall flux as a function of increased electro-migration and pH of the respective molecules. RESULTS: In a high flux hemodialyzer, the effective diffusivities of endothelin, cystatin C, and interleukin – 6 are 15.00 x 10(-10) cm(2)/s, 7.7 x 10(-10) cm(2)/s, and 5.4 x 10(-10) cm(2)/s, respectively, through the capillaries’ walls. In a nanofabricated membrane, the effective diffusivities of endothelin, cystatin C, and interleukin – 6 are 13.87 x 10(-7) cm(2)/s, 5.73 x 10(-7) cm(2)/s, and 3.45 x 10(-7) cm(2)/s, respectively, through a nanofabricated membrane. Theoretical modeling showed that a 96% reduction in the membrane's thickness and the application of an electric potential of 10 mV across the membrane could enhance the flux of endothelin, cystatin C, and interleukin - 6 by a factor of 25. A ΔpH of 0.07 altered the fluxes minimally. CONCLUSIONS: Nanofabricated hemodialysis membranes with a reduced thickness and an applied electric potential can enhance the effective diffusivity and electro-migration flux of the respective uremic toxins by 3 orders of magnitude as compared to those passing through the high flux hemodialyzer.
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spelling pubmed-39620912014-03-31 Study of Uremic Toxin Fluxes Across Nanofabricated Hemodialysis Membranes Using Irreversible Thermodynamics Hedayat, Assem Peace, Rob Elmoselhi, Hamdi Shoker, Ahmed Comput Struct Biotechnol J Research Article INTRODUCTION: The flux of uremic toxin middle molecules through currently used hemodialysis membranes is suboptimal, mainly because of the membranes’ pore architecture. AIM: Identifying the modifiable sieving parameters that can be improved by nanotechnology to enhance fluxes of uremic toxins across the walls of dialyzers’ capillaries. METHODS: We determined the maximal dimensions of endothelin, cystatin C, and interleukin – 6 using the macromolecular modeling software, COOT. We also applied the expanded Nernst-Plank equation to calculate the changes in the overall flux as a function of increased electro-migration and pH of the respective molecules. RESULTS: In a high flux hemodialyzer, the effective diffusivities of endothelin, cystatin C, and interleukin – 6 are 15.00 x 10(-10) cm(2)/s, 7.7 x 10(-10) cm(2)/s, and 5.4 x 10(-10) cm(2)/s, respectively, through the capillaries’ walls. In a nanofabricated membrane, the effective diffusivities of endothelin, cystatin C, and interleukin – 6 are 13.87 x 10(-7) cm(2)/s, 5.73 x 10(-7) cm(2)/s, and 3.45 x 10(-7) cm(2)/s, respectively, through a nanofabricated membrane. Theoretical modeling showed that a 96% reduction in the membrane's thickness and the application of an electric potential of 10 mV across the membrane could enhance the flux of endothelin, cystatin C, and interleukin - 6 by a factor of 25. A ΔpH of 0.07 altered the fluxes minimally. CONCLUSIONS: Nanofabricated hemodialysis membranes with a reduced thickness and an applied electric potential can enhance the effective diffusivity and electro-migration flux of the respective uremic toxins by 3 orders of magnitude as compared to those passing through the high flux hemodialyzer. Research Network of Computational and Structural Biotechnology (RNCSB) Organization 2013-06-11 /pmc/articles/PMC3962091/ /pubmed/24688713 http://dx.doi.org/10.5936/csbj.201303005 Text en © Hedayat et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly cited.
spellingShingle Research Article
Hedayat, Assem
Peace, Rob
Elmoselhi, Hamdi
Shoker, Ahmed
Study of Uremic Toxin Fluxes Across Nanofabricated Hemodialysis Membranes Using Irreversible Thermodynamics
title Study of Uremic Toxin Fluxes Across Nanofabricated Hemodialysis Membranes Using Irreversible Thermodynamics
title_full Study of Uremic Toxin Fluxes Across Nanofabricated Hemodialysis Membranes Using Irreversible Thermodynamics
title_fullStr Study of Uremic Toxin Fluxes Across Nanofabricated Hemodialysis Membranes Using Irreversible Thermodynamics
title_full_unstemmed Study of Uremic Toxin Fluxes Across Nanofabricated Hemodialysis Membranes Using Irreversible Thermodynamics
title_short Study of Uremic Toxin Fluxes Across Nanofabricated Hemodialysis Membranes Using Irreversible Thermodynamics
title_sort study of uremic toxin fluxes across nanofabricated hemodialysis membranes using irreversible thermodynamics
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3962091/
https://www.ncbi.nlm.nih.gov/pubmed/24688713
http://dx.doi.org/10.5936/csbj.201303005
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