Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/25217
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dc.contributor.authorUzun, Lokman-
dc.contributor.authorYavuz, Handan-
dc.contributor.authorÇelik, Hamdi-
dc.contributor.authorDenizli, Adil-
dc.date.accessioned2022-03-21T08:45:26Z-
dc.date.available2022-03-21T08:45:26Z-
dc.date.issued2010-07-01-
dc.identifier.citationUzun, L. vd. (2010). "Poly(hydroxyethyl methacrylate) based affinity membranes for in vitro removal of anti-dsDNA antibodies from SLE plasma". International Journal of Biological Macromolecules, 47(1), 44-49.en_US
dc.identifier.issn0141-8130-
dc.identifier.issn1879-0003-
dc.identifier.urihttps://doi.org/10.1016/j.ijbiomac.2010.03.022-
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0141813010001157-
dc.identifier.urihttp://hdl.handle.net/11452/25217-
dc.description.abstractThe preparation of polymeric membrane using affinity technology for application in blood filtration devices is described here. DNA attached poly( hydroxyethyl methacrylate) (PHEMA) based microporous affinity membrane was prepared for selective removal of anti-dsDNA antibodies from systemic lupus erythematosus (SLE) patient plasma in in vitro. In order to further increase blood-compatibility of affinity membrane, aminoacid based comonomer N-methacryloyl-L-alanine (MAAL) was included in the polymerization recipe. PHEMAAL membrane was produced by a photopolymerization technique and then characterized by swelling tests and scanning electron microscope (SEM) studies. Blood-compatibility tests were also performed. The water swelling ratio of PHEMAAL membrane increased significantly (133.2%) compared with PHEMA (58%). PHEMAAL membrane has large pores around in the range of 5-10 mu m. All the clotting times increased when compared with PHEMA membrane. Loss of platelets and leukocytes was very low. DNA loading was 7.8 mg/g. There was a very low anti-dsDNA-antibody adsorption onto the plain PHEMAAL membrane, about 78 IU/g. The PHEMAAL-DNA membrane adsorbed anti-dsDNA-antibody in the range of 10-68 x 10(3) IU/g from SLE plasma. Anti-dsDNA-antibody concentration decreased significantly from 875 to 144 IU/ml with the time. Anti-dsDNA-antibodies could be repeatedly adsorbed and eluted without noticeable loss in the anti-dsDNA-antibody adsorption amount.en_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAntibody removalen_US
dc.subjectPHEMAen_US
dc.subjectAffinity membranesen_US
dc.subjectDNAen_US
dc.subjectSLEen_US
dc.subjectSystemic-lupus-erythematosusen_US
dc.subjectImmobilized polyhydroxyethylmethacrylate microbeadsen_US
dc.subjectImprinted supermacroporous cryogelsen_US
dc.subjectHuman-immunoglobulin-Gen_US
dc.subjectCholesterol removalen_US
dc.subjectDNA immunoadsorbenten_US
dc.subjectChromatographyen_US
dc.subjectIGGen_US
dc.subjectPurificationen_US
dc.subjectAdsorptionen_US
dc.subjectBiochemistry & molecular biologyen_US
dc.subjectChemistryen_US
dc.subjectPolymer scienceen_US
dc.subject.meshAdsorptionen_US
dc.subject.meshAntibodies, antinuclearen_US
dc.subject.meshBlood coagulationen_US
dc.subject.meshFemaleen_US
dc.subject.meshHumansen_US
dc.subject.meshLupus erythematosusen_US
dc.subject.meshSystemicen_US
dc.subject.meshMaleen_US
dc.subject.meshMaterials testingen_US
dc.subject.meshMembranes, artificialen_US
dc.subject.meshPlasmaen_US
dc.subject.meshPolyhydroxyethyl Methacrylateen_US
dc.subject.meshPorosityen_US
dc.titlePoly(hydroxyethyl methacrylate) based affinity membranes for in vitro removal of anti-dsDNA antibodies from SLE plasmaen_US
dc.typeArticleen_US
dc.identifier.wos000278695000009tr_TR
dc.identifier.scopus2-s2.0-77953020673tr_TR
dc.relation.tubitak105S360tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Fen-Edebiyat Fakültesi/Kimya Bölümü.tr_TR
dc.identifier.startpage44tr_TR
dc.identifier.endpage49tr_TR
dc.identifier.volume47tr_TR
dc.identifier.issue1tr_TR
dc.relation.journalInternational Journal of Biological Macromoleculesen_US
dc.contributor.buuauthorOsman, Bilgen-
dc.contributor.researcheridABF-4791-2020tr_TR
dc.relation.collaborationYurt içitr_TR
dc.identifier.pubmed20381519tr_TR
dc.subject.wosBiochemistry & molecular biologyen_US
dc.subject.wosChemistry, applieden_US
dc.subject.wosPolymer scienceen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.indexed.pubmedPubMeden_US
dc.wos.quartileQ3 (Biochemistry & molecular biology)en_US
dc.contributor.scopusid15221651200tr_TR
dc.subject.scopusCibacron Blue F 3Ga; Cryogels; Muramidaseen_US
dc.subject.emtreeAlanineen_US
dc.subject.emtreeDouble stranded DNA antibodyen_US
dc.subject.emtreePolymaconen_US
dc.subject.emtreeAntibody affinityen_US
dc.subject.emtreeArticleen_US
dc.subject.emtreeBlood clotting testen_US
dc.subject.emtreeBlood clotting timeen_US
dc.subject.emtreeBlood compatibilityen_US
dc.subject.emtreeCell adhesionen_US
dc.subject.emtreeChemical structureen_US
dc.subject.emtreeControlled studyen_US
dc.subject.emtreeHumanen_US
dc.subject.emtreeHuman cellen_US
dc.subject.emtreeHydrophilicityen_US
dc.subject.emtreeImmunoadsorptionen_US
dc.subject.emtreeIn vitro studyen_US
dc.subject.emtreeLeukocyte counten_US
dc.subject.emtreePartial thromboplastin timeen_US
dc.subject.emtreePolymerizationen_US
dc.subject.emtreeProthrombin timeen_US
dc.subject.emtreeScanning electron microscopyen_US
dc.subject.emtreeSystemic lupus erythematosusen_US
dc.subject.emtreeThrombocyte counten_US
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