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Immunoreaction-Triggered Diagnostic Device Using Reduced Graphene Oxide/Cuo Nps/Chitosan Ternary Nanocomposite, Toward Enhanced Electrochemical Detection of Albumin Publisher



Feyzibarnaji B1 ; Darbasizadeh B2 ; Arkan E3 ; Salehzadeh H4 ; Salimi A5 ; Nili F6 ; Dinarvand R1, 7, 8 ; Mohammadi A7, 8
Authors
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Authors Affiliations
  1. 1. Department of Pharmaceutical Nanotechnology, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran
  2. 2. Student Research Committee, Department of Pharmaceutics and Pharmaceutical Nanotechnology, School of Pharmacy, Shahid Beheshti University of Medical Sciences, Tehran, Iran
  3. 3. Nano Drug Delivery research center, Kermanshah University of Medical Sciences, Kermanshah, Iran
  4. 4. Faculty of Chemistry, Kharazmi University, Tehran, Iran
  5. 5. Department of Chemistry, University of Kurdistan, Sanandaj, Iran
  6. 6. Department of Pathology, Imam Khomini Hospital Complex, Tehran University of Medical Sciences, Tehran, Iran
  7. 7. Department of Drug and Food Control, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran
  8. 8. Department of Drug and Food Control, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran

Source: Journal of Electroanalytical Chemistry Published:2020


Abstract

Determination of Human Serum Albumin (HSA), an important biomarker, is needed for early diagnosis and therapy monitoring in a variety of diseases. A novel electrochemical immunosensor was constructed to detect HSA in both standard solutions and human serum samples. In so doing, glassy carbon electrode (GCE) was modified in three steps. First, graphene oxide (GO) was drop-casted on the GCE surface and electrochemically reduced. Second, in situ electrochemical deposition (ECD) of cupric oxide nanoparticles (CuO NPs) in two consecutive steps has been done. Finally, anti-HSA antibodies have been immobilized via amino groups of chitosan which drop-casted earlier. The surface morphology and nature of the modified electrode was characterized using common electrochemical and imaging techniques. Using differential pulse voltammetry (DPV), the response of the immunosensor was linear in the range of 10–450 ng.mL−1 HSA, with the limit of detection (LOD) 2.6 ng.mL−1. Moreover, the selectivity of the modified electrode was investigated to some common interferences. Under optimum conditions, the immunosensor displayed excellent stability, reproducibility, selectivity and repeatability. The findings indicated that fabricated electrode is a promising candidate for quantifying HSA that is applicable in diagnostics and therapeutics. © 2020 Elsevier B.V.