Macroporous Composite Cryogels with Embedded Polystyrene Divinylbenzene Microparticles for the Adsorption of Toxic Metabolites from Blood

Composite monolithic adsorbents were prepared by the incorporation of neutral polystyrene divinylbenzene (PS-DVB) microparticles into macroporous polymer structures produced by cryogelation of agarose or poly(vinyl alcohol). The composite materials exhibited excellent flow-through properties. Scanni...

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Main Authors: Tanja Eichhorn, Alexander E. Ivanov, Maria B. Dainiak, André Leistner, Ingrid Linsberger, Hans Jungvid, Sergey V. Mikhalovsky, Viktoria Weber
Format: Article
Language:English
Published: Wiley 2013-01-01
Series:Journal of Chemistry
Online Access:http://dx.doi.org/10.1155/2013/348412
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author Tanja Eichhorn
Alexander E. Ivanov
Maria B. Dainiak
André Leistner
Ingrid Linsberger
Hans Jungvid
Sergey V. Mikhalovsky
Viktoria Weber
author_facet Tanja Eichhorn
Alexander E. Ivanov
Maria B. Dainiak
André Leistner
Ingrid Linsberger
Hans Jungvid
Sergey V. Mikhalovsky
Viktoria Weber
author_sort Tanja Eichhorn
collection DOAJ
description Composite monolithic adsorbents were prepared by the incorporation of neutral polystyrene divinylbenzene (PS-DVB) microparticles into macroporous polymer structures produced by cryogelation of agarose or poly(vinyl alcohol). The composite materials exhibited excellent flow-through properties. Scanning electron microscopy of the composite cryogels revealed that the microparticles were covered by thin films of poly(vinyl alcohol) or agarose and thus were withheld in the monolith structure. Plain PS-DVB microparticles showed efficient adsorption of albumin-bound toxins related to liver failure (bilirubin and cholic acid) and of cytokines (tumor necrosis factor-alpha and interleukin-6). The rates of adsorption and the amount of adsorbed factors were lower for the embedded microparticles as compared to the parent PS-DVB microparticles, indicating the importance of the accessibility of the adsorbent pores. Still, the macroporous composite materials showed efficient adsorption of albumin-bound toxins related to liver failure as well as efficient binding of cytokines, combined with good blood compatibility. Thus, the incorporation of microparticles into macroporous polymer structures may provide an option for the development of adsorption modules for extracorporeal blood purification.
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institution Kabale University
issn 2090-9063
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language English
publishDate 2013-01-01
publisher Wiley
record_format Article
series Journal of Chemistry
spelling doaj-art-9a37799ccdc74c16bcf34a04d822c58b2025-02-03T05:50:23ZengWileyJournal of Chemistry2090-90632090-90712013-01-01201310.1155/2013/348412348412Macroporous Composite Cryogels with Embedded Polystyrene Divinylbenzene Microparticles for the Adsorption of Toxic Metabolites from BloodTanja Eichhorn0Alexander E. Ivanov1Maria B. Dainiak2André Leistner3Ingrid Linsberger4Hans Jungvid5Sergey V. Mikhalovsky6Viktoria Weber7Center for Biomedical Technology, Danube University Krems, Dr.-Karl-Dorrek-Strasse 30, 3500 Krems, AustriaProtista Biotechnology AB, Kvarngatan 2, 26734 Bjuv, SwedenProtista Biotechnology AB, Kvarngatan 2, 26734 Bjuv, SwedenPolymerics GmbH, Landsberger Allee 378, 12681 Berlin, GermanyCenter for Biomedical Technology, Danube University Krems, Dr.-Karl-Dorrek-Strasse 30, 3500 Krems, AustriaProtista Biotechnology AB, Kvarngatan 2, 26734 Bjuv, SwedenSchool of Pharmacy and Biomolecular Sciences, University of Brighton, Brighton BN2 4GJ, UKCenter for Biomedical Technology, Danube University Krems, Dr.-Karl-Dorrek-Strasse 30, 3500 Krems, AustriaComposite monolithic adsorbents were prepared by the incorporation of neutral polystyrene divinylbenzene (PS-DVB) microparticles into macroporous polymer structures produced by cryogelation of agarose or poly(vinyl alcohol). The composite materials exhibited excellent flow-through properties. Scanning electron microscopy of the composite cryogels revealed that the microparticles were covered by thin films of poly(vinyl alcohol) or agarose and thus were withheld in the monolith structure. Plain PS-DVB microparticles showed efficient adsorption of albumin-bound toxins related to liver failure (bilirubin and cholic acid) and of cytokines (tumor necrosis factor-alpha and interleukin-6). The rates of adsorption and the amount of adsorbed factors were lower for the embedded microparticles as compared to the parent PS-DVB microparticles, indicating the importance of the accessibility of the adsorbent pores. Still, the macroporous composite materials showed efficient adsorption of albumin-bound toxins related to liver failure as well as efficient binding of cytokines, combined with good blood compatibility. Thus, the incorporation of microparticles into macroporous polymer structures may provide an option for the development of adsorption modules for extracorporeal blood purification.http://dx.doi.org/10.1155/2013/348412
spellingShingle Tanja Eichhorn
Alexander E. Ivanov
Maria B. Dainiak
André Leistner
Ingrid Linsberger
Hans Jungvid
Sergey V. Mikhalovsky
Viktoria Weber
Macroporous Composite Cryogels with Embedded Polystyrene Divinylbenzene Microparticles for the Adsorption of Toxic Metabolites from Blood
Journal of Chemistry
title Macroporous Composite Cryogels with Embedded Polystyrene Divinylbenzene Microparticles for the Adsorption of Toxic Metabolites from Blood
title_full Macroporous Composite Cryogels with Embedded Polystyrene Divinylbenzene Microparticles for the Adsorption of Toxic Metabolites from Blood
title_fullStr Macroporous Composite Cryogels with Embedded Polystyrene Divinylbenzene Microparticles for the Adsorption of Toxic Metabolites from Blood
title_full_unstemmed Macroporous Composite Cryogels with Embedded Polystyrene Divinylbenzene Microparticles for the Adsorption of Toxic Metabolites from Blood
title_short Macroporous Composite Cryogels with Embedded Polystyrene Divinylbenzene Microparticles for the Adsorption of Toxic Metabolites from Blood
title_sort macroporous composite cryogels with embedded polystyrene divinylbenzene microparticles for the adsorption of toxic metabolites from blood
url http://dx.doi.org/10.1155/2013/348412
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