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Electrochemiluminescent immunosensor for detection of carcinoembryonic antigen using luminol-coated silver nanoparticles.
Akbari Nakhjavani, Sattar; Khalilzadeh, Balal; Afsharan, Hadi; Hosseini, Nashmin; Ghahremani, Mohammad Hossein; Carrara, Sandro; Tasoglu, Savas; Omidi, Yadollah.
Afiliação
  • Akbari Nakhjavani S; Mechanical Engineering Department, School of Engineering, Koç University, Istanbul, Turkey, 34450. sakbarinakhjavani@ku.edu.tr.
  • Khalilzadeh B; Department of Molecular Medicine, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Tehran, Iran. sakbarinakhjavani@ku.edu.tr.
  • Afsharan H; Koç University Translational Medicine Research Center (KUTTAM), Koç University, Istanbul, Turkey, 34450. sakbarinakhjavani@ku.edu.tr.
  • Hosseini N; Stem Cell Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
  • Ghahremani MH; Optical+Biomedical Engineering Laboratory, Department of Electrical, Electronic and Computer Engineering, University of Western Australia, Perth, WA, 6009, Australia.
  • Carrara S; Research Center for Pharmaceutical Nanotechnology, Biomedicine Institute, Tabriz University of Medical Sciences, Tabriz, Iran.
  • Tasoglu S; Faculty of Pharmacy, Department of Pharmaceutics, Tabriz University of Medical Sciences, Tabriz, Iran.
  • Omidi Y; Department of Molecular Medicine, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Mikrochim Acta ; 190(2): 77, 2023 01 30.
Article em En | MEDLINE | ID: mdl-36715890
ABSTRACT
Recently, electrochemiluminescent (ECL) immunosensors have received much attention in the field of biomarker detection. Here, a highly enhanced ECL immunosensing platform was designed for ultrasensitive detection of carcinoembryonic antigen (CEA). The surface of the glassy carbon electrode was enhanced by applying functional nanostructures such as thiolated graphene oxide (S-GO) and streptavidin-coated gold nanoparticles (SA-AuNPs). The selectivity and sensitivity of the designed immunosensor were improved by entrapping CEA biomolecules using a sandwich approach. Luminol/silver nanoparticles (Lu-SNPs) were applied as the main core of the signaling probe, which were then coated with streptavidin to provide overloading of the secondary antibody. The highly ECL signal enhancement was obtained due to the presence of horseradish peroxidase (HRP) in the signaling probe, in which the presence of H2O2 further amplified the intensity of the signals. The engineered immunosensor presented excellent sensitivity for CEA detection, with limit of detection (LOD) and linear detection range (LDR) values of 58 fg mL-1 and 0.1 pg mL-1 to 5 pg mL-1 (R2 = 0.9944), respectively. Besides its sensitivity, the fabricated ECL immunosensor presented outstanding selectivity for the detection of CEA in the presence of various similar agents. Additionally, the developed immunosensor showed an appropriate repeatability (RSD 3.8%) and proper stability (2 weeks). Having indicated a robust performance in the real human serum with stated LOD and LDR, the engineered immunosensor can be considered for the detection and monitoring of CEA in the clinic.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article