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Label-free electrochemical aptasensor for rapid detection of SARS-CoV-2 spike glycoprotein based on the composite of Cu(OH)(2) nanorods arrays as a high-performance surface substrate

The development of advanced electrode materials and the combination of aptamer with them have improved dramatically the performance of aptasensors. Herein, a new architecture based on copper hydroxide nanorods (Cu(OH)(2) NRs) are directly grown on the surface of screen printed carbon electrode (SPCE...

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Detalles Bibliográficos
Autores principales: Rahmati, Zeinab, Roushani, Mahmoud, Hosseini, Hadi, Choobin, Hamzeh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier B.V. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8940256/
https://www.ncbi.nlm.nih.gov/pubmed/35339949
http://dx.doi.org/10.1016/j.bioelechem.2022.108106
Descripción
Sumario:The development of advanced electrode materials and the combination of aptamer with them have improved dramatically the performance of aptasensors. Herein, a new architecture based on copper hydroxide nanorods (Cu(OH)(2) NRs) are directly grown on the surface of screen printed carbon electrode (SPCE) using a two-step in situ, very simple and fast strategy and was used as a high-performance substrate for immobilization of aptamer strings, as well as an electrochemical probe to development a label-free electrochemical aptasensor for SARS-CoV-2 spike glycoprotein measurement. The Cu(OH)(2) NRs was characterized using X-ray Diffraction (XRD) and electron microscopy (FESEM). In the presence of SARS-CoV-2 spike glycoprotein, a decrease in Cu(OH)(2) NRs-associated peak current was observed that can be owing to the target-aptamer complexes formation and thus blocking the electron transfer of Cu(OH)(2) NRs on the surface of electrode. This strategy exhibited wide dynamic range in of 0.1 fg mL(−1) to 1.2 µg mL(−1) and with a high sensitivity of 1974.43 μA mM(−1) cm(−2) and low detection limit of 0.03 ± 0.01 fg mL(−1) of SARS-CoV-2 spike glycoprotein deprived of any cross-reactivity in the presence of possible interference species. In addition, the good reproducibility, repeatability, high stability and excellent feasibility in real samples of saliva and viral transport medium (VTM) were found from the provided aptasensor. Also, the aptasensor efficiency was evaluated by real samples of sick and healthy individuals and compared with the standard polymerase chain reaction (PCR) method and acceptable results were observed.