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In Situ Growth of CuWO(4) Nanospheres over Graphene Oxide for Photoelectrochemical (PEC) Immunosensing of Clinical Biomarker

Procalcitonin (PCT) protein has recently been identified as a clinical marker for bacterial infections based on its better sepsis sensitivity. Thus, an increased level of PCT could be linked with disease diagnosis and therapeutics. In this study, we describe the construction of the photoelectrochemi...

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Detalles Bibliográficos
Autores principales: Abbas, Zaheer, Soomro, Razium Ali, Kalwar, Nazar Hussain, Tunesi, Mawada, Willander, Magnus, Karakuş, Selcan, Kilislioğlu, Ayben
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6983212/
https://www.ncbi.nlm.nih.gov/pubmed/31881686
http://dx.doi.org/10.3390/s20010148
Descripción
Sumario:Procalcitonin (PCT) protein has recently been identified as a clinical marker for bacterial infections based on its better sepsis sensitivity. Thus, an increased level of PCT could be linked with disease diagnosis and therapeutics. In this study, we describe the construction of the photoelectrochemical (PEC) PCT immunosensing platform based on it situ grown photo-active CuWO(4) nanospheres over reduced graphene oxide layers (CuWO(4)@rGO). The in situ growth strategy enabled the formation of small nanospheres (diameter of 200 nm), primarily composed of tiny self-assembled CuWO(4) nanoparticles (2–5 nm). The synergic coupling of CuWO(4) with rGO layers constructed an excellent photo-active heterojunction for photoelectrochemical (PEC) sensing. The platform was then considered for electrocatalytic (EC) mechanism-based detection of PCT, where inhibition of the photocatalytic oxidation signal of ascorbic acid (AA), subsequent to the antibody–antigen interaction, was recorded as the primary signal response. This inhibition detection approach enabled sensitive detection of PCT in a concentration range of 10 pg·mL(−1) to 50 ng.mL(−1) with signal sensitivity achievable up to 0.15 pg·mL(−1). The proposed PEC hybrid (CuWO(4)@rGO) could further be engineered to detect other clinically important species.