Molecularly imprinted based surface plasmon resonance nanosensors for microalbumin detection
dc.authorid | 0000-0003-2245-8074 | en_US |
dc.authorid | 0000-0003-3260-1639 | |
dc.contributor.author | Esentürk, Meltem Koca | |
dc.contributor.author | Akgönüllü, Semra | |
dc.contributor.author | Yılmaz, Fatma | |
dc.contributor.author | Denizli, Adil | |
dc.date.accessioned | 2021-06-23T19:51:41Z | |
dc.date.available | 2021-06-23T19:51:41Z | |
dc.date.issued | 2019 | |
dc.department | BAİBÜ, Gerede Meslek Yüksekokulu, Kimya Ve Kimyasal İşleme Teknolojileri Bölümü | en_US |
dc.description.abstract | Human serum albumin (HSA) is a major blood plasma protein also found in urine where its existence may be a marker of some types of liver or kidney dysfunction. Herein, we fabricated a novel surface plasmon resonance (SPR) nanosensor for selective, sensitive, and label-free microalbumin detection both in aqueous and urine sample solutions. First, HSA-imprinted nanoparticles were synthesized, which consist of ethylene glycol dimethacrylate and N-methacryloyl-L-leucine methyl ester as a cross-linker and functional monomer. The nanoparticles were characterized by zeta-size and scanning electron microscope analyses and were dropped onto the SPR chip surface to make HSA sensitive nanosensor. Characterization studies of HSA-imprinted SPR chip were carried out by atomic force microscopy, Fourier-transform infrared spectroscopy, contact angle, and ellipsometer. The limit of detection and limit of quantification values of HSA-imprinted SPR nanosensor were calculated as 0.7pM and 1.9pM for the concentration range of 0.15-500nM. Selectivity studies of HSA-imprinted SPR nanosensor were achieved with hemoglobin and transferrin proteins which were chosen as competitor molecules. HSA-imprinted SPR nanosensor was displayed highly selective and sensitive to HSA. | en_US |
dc.identifier.doi | 10.1080/09205063.2019.1600181 | |
dc.identifier.endpage | 661 | en_US |
dc.identifier.issn | 0920-5063 | |
dc.identifier.issn | 1568-5624 | |
dc.identifier.issue | 8 | en_US |
dc.identifier.pmid | 30920349 | en_US |
dc.identifier.scopus | 2-s2.0-85063972206 | en_US |
dc.identifier.scopusquality | Q2 | en_US |
dc.identifier.startpage | 646 | en_US |
dc.identifier.uri | https://doi.org/10.1080/09205063.2019.1600181 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12491/10029 | |
dc.identifier.volume | 30 | en_US |
dc.identifier.wos | WOS:000467749600004 | en_US |
dc.identifier.wosquality | Q2 | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.indekslendigikaynak | PubMed | en_US |
dc.institutionauthor | Yılmaz, Fatma | |
dc.language.iso | en | en_US |
dc.publisher | Taylor & Francis Ltd | en_US |
dc.relation.ispartof | Journal Of Biomaterials Science-Polymer Edition | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | Microalbumin Detection | en_US |
dc.subject | Nanoparticles | en_US |
dc.subject | Surface Plasmon Resonance | en_US |
dc.subject | Nanosensor | en_US |
dc.title | Molecularly imprinted based surface plasmon resonance nanosensors for microalbumin detection | en_US |
dc.type | Article | en_US |
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