Selective removal of the autoantibodies from rheumatoid arthritis patient plasma using protein A carrying affinity cryogels
dc.contributor.author | Alkan, Huseyin | |
dc.contributor.author | Bereli, Nilay | |
dc.contributor.author | Baysal, Zubeyde | |
dc.contributor.author | Denizli, Adil | |
dc.date.accessioned | 2024-04-24T16:10:54Z | |
dc.date.available | 2024-04-24T16:10:54Z | |
dc.date.issued | 2010 | |
dc.department | Dicle Üniversitesi | en_US |
dc.description.abstract | Rheumatoid arthritis is a chronic, progressive, deabilitating autoimmune disease that occurs in approximately 1% of adults. Rheumatoid arthritis is characterized by chronic polyarthritis and destruction of multiple joints. In this study, IgM-antibody removal from human plasma with supermacroporous poly(hydroxyethyl methacrylate) [PHEMA] cryogel carrying protein A has been evaluated. The PHEMA cryogel was prepared by bulk polymerization which proceeds in an aqueous solution of monomer frozen inside a plastic syringe (cryo-polymerization). After thawing, the PHEMA cryogel contains a continuous matrix having interconnected macropores of 10-200 mu m size. Pore volume in the PHEMA cryogel was 71.6%. Protein A molecules were covalently immobilized onto the PHEMA cryogel via cyanogen bromide (CNBr) activation. The PHEMA cryogel was contacted with blood in in vitro system for the determination of blood-compatibility. The supermacroporous structure of the PHEMA cryogel makes it possible to process blood cells without blocking the cryogel column. IgM-antibody adsorption capacity decreased significantly with the increase of the plasma flow-rate. The maximum IgM-antibody adsorption amount was 42.7 mg/g. IgM-antibody molecules could be repeatedly adsorbed and eluted without noticeable loss in the IgM-antibody adsorption amount. (C) 2010 Elsevier B.V. All rights reserved. | en_US |
dc.identifier.doi | 10.1016/j.bej.2010.06.010 | |
dc.identifier.endpage | 159 | en_US |
dc.identifier.issn | 1369-703X | |
dc.identifier.issn | 1873-295X | |
dc.identifier.issue | 3 | en_US |
dc.identifier.scopus | 2-s2.0-77955419442 | |
dc.identifier.scopusquality | Q2 | |
dc.identifier.startpage | 153 | en_US |
dc.identifier.uri | https://doi.org/10.1016/j.bej.2010.06.010 | |
dc.identifier.uri | https://hdl.handle.net/11468/15179 | |
dc.identifier.volume | 51 | en_US |
dc.identifier.wos | WOS:000281936900009 | |
dc.identifier.wosquality | Q1 | |
dc.indekslendigikaynak | Web of Science | |
dc.indekslendigikaynak | Scopus | |
dc.language.iso | en | en_US |
dc.publisher | Elsevier | en_US |
dc.relation.ispartof | Biochemical Engineering Journal | |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Rheumatoid Arthritis | en_US |
dc.subject | Phema | en_US |
dc.subject | Antibody Removal | en_US |
dc.subject | Affinity Therapy | en_US |
dc.subject | Cryogels | en_US |
dc.title | Selective removal of the autoantibodies from rheumatoid arthritis patient plasma using protein A carrying affinity cryogels | en_US |
dc.title | Selective removal of the autoantibodies from rheumatoid arthritis patient plasma using protein A carrying affinity cryogels | |
dc.type | Article | en_US |