A novel adsorbent for protein chromatography: Supermacroporous monolithic cryogel embedded with Cu2+-attached sporopollenin particles
dc.contributor.author | Erzengin, Mahmut | |
dc.contributor.author | Ünlü, Nuri | |
dc.contributor.author | Odabaşı, Mehmet | |
dc.date.accessioned | 13.07.201910:50:10 | |
dc.date.accessioned | 2019-07-29T19:26:18Z | |
dc.date.available | 13.07.201910:50:10 | |
dc.date.available | 2019-07-29T19:26:18Z | |
dc.date.issued | 2011 | |
dc.department | Sabire Yazıcı Fen Edebiyat Fakültesi | |
dc.description.abstract | The aim of this study is to prepare supermacroporous cryogels embedded with Cu2+-attached sporopollenin particles (Cu2+-ASP) having large surface area for high protein adsorption capacity. Super-macroporous poly(2-hydroxyethyl methacrylate) (PHEMA)-based monolithic cryogel column embedded with Cu2+-ASP was prepared by radical cryo-copolymerization of 2-hydroxyethyl methacrylate (HEMA) with N,N'-methylene-bis-acrylamide (MBAAm) as cross-linker directly in a plastic syringe for affinity purification of human serum albumin (HSA). Firstly, Cu2+ ions were attached to sporopollenin particles (SP), then the supermacroporous PHEMA cryogel with embedded Cu2+-ASP was produced by free radical polymerization using N,N,N',N'-tetramethylene diamine (TEMED) and ammonium persulfate (APS) as initiator/activator pair in an ice bath. Embedded particles (10 mg) in PHEMA-based cryogel column were used in the adsorption/desorption of HSA from aqueous solutions. Optimum conditions of adsorption experiments were performed at pH 8.0 phosphate buffer, with flow rate of 0.5 mL/min, and at 5 degrees C. The maximum amount of HSA adsorption from aqueous solution was very high (677.4 mg/g SP) with initial concentration 6 mg/mL It was observed that HSA could be repeatedly adsorbed and desorbed to the embedded Cu2+-ASP in PHEMA cryogel without significant loss of adsorption capacity. (C) 2010 Elsevier B.V. All rights reserved. | |
dc.identifier.doi | 10.1016/j.chroma.2010.11.074 | |
dc.identifier.endpage | 490 | en_US |
dc.identifier.issn | 0021-9673 | |
dc.identifier.issue | 3 | en_US |
dc.identifier.pmid | 21176840 | |
dc.identifier.scopusquality | Q1 | |
dc.identifier.startpage | 484 | en_US |
dc.identifier.uri | https://doi.org/10.1016/j.chroma.2010.11.074 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12451/5530 | |
dc.identifier.volume | 1218 | en_US |
dc.identifier.wos | WOS:000286680900015 | |
dc.identifier.wosquality | N/A | |
dc.indekslendigikaynak | Web of Science | |
dc.indekslendigikaynak | Scopus | |
dc.indekslendigikaynak | PubMed | |
dc.language.iso | en | |
dc.publisher | Elsevier Ltd. | |
dc.relation.ispartof | Journal of Chramatography A | |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | |
dc.rights | info:eu-repo/semantics/closedAccess | |
dc.subject | Protein Adsorption | |
dc.subject | Cryogels | |
dc.subject | Sporopollenin | |
dc.subject | Metal Chelate | |
dc.subject | Particle Embedding | |
dc.title | A novel adsorbent for protein chromatography: Supermacroporous monolithic cryogel embedded with Cu2+-attached sporopollenin particles | |
dc.type | Article |
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