Nanostructured materials have potential as platforms for analytical assays and catalytic reactions. Herein, we report the synthesis of electrocatalytically active cobalt phosphate nanostructures (CPNs) using a simple, low-cost, and scalable preparation method. The electrocatalytic properties of CPNs toward the electrooxidation of glucose (Glu) were studied by cyclic voltammetry and chronoamperometry in relevant biological electrolytes, such as phosphate-buffered saline (PBS), at physiological pH (7.4). Using CPNs, Glu detection could be achieved over a wide range of biologically relevant concentrations, from 1 to 30 mM Glu in PBS, with a sensitivity of 7.90 nA/mM cm2 and a limit of detection of 0.3 mM, thus fulfilling the necessary requirements for human blood Glu detection. In addition, CPNs showed a high structural and functional stability over time at physiological pH. The CPN-coated electrodes could also be used for Glu detection in the presence of interfering agents (e.g., ascorbic acid and dopamine) and in human serum. Density functional theory calculations were performed to evaluate the interaction of Glu with different faceted cobalt phosphate surfaces; the results revealed that specific surface presentations of under-coordinated cobalt led to the strongest interaction with Glu, suggesting that enhanced detection of Glu by CPNs can be achieved by lowering the surface coordination of cobalt. Our results highlight the potential use of phosphate-based nanostructures as catalysts for electrochemical sensing of biochemical analytes.

Tomanin, P.p., Cherepanov, P.v., Besford, Q.a., Christofferson, A.j., Amodio, A., Mcconville, C.f., et al. (2018). Cobalt phosphate nanostructures for non-enzymatic glucose sensing at physiological pH. ACS APPLIED MATERIALS & INTERFACES, 10(49), 42786-42795 [10.1021/acsami.8b12966].

Cobalt phosphate nanostructures for non-enzymatic glucose sensing at physiological pH

Cavalieri F.
2018-01-01

Abstract

Nanostructured materials have potential as platforms for analytical assays and catalytic reactions. Herein, we report the synthesis of electrocatalytically active cobalt phosphate nanostructures (CPNs) using a simple, low-cost, and scalable preparation method. The electrocatalytic properties of CPNs toward the electrooxidation of glucose (Glu) were studied by cyclic voltammetry and chronoamperometry in relevant biological electrolytes, such as phosphate-buffered saline (PBS), at physiological pH (7.4). Using CPNs, Glu detection could be achieved over a wide range of biologically relevant concentrations, from 1 to 30 mM Glu in PBS, with a sensitivity of 7.90 nA/mM cm2 and a limit of detection of 0.3 mM, thus fulfilling the necessary requirements for human blood Glu detection. In addition, CPNs showed a high structural and functional stability over time at physiological pH. The CPN-coated electrodes could also be used for Glu detection in the presence of interfering agents (e.g., ascorbic acid and dopamine) and in human serum. Density functional theory calculations were performed to evaluate the interaction of Glu with different faceted cobalt phosphate surfaces; the results revealed that specific surface presentations of under-coordinated cobalt led to the strongest interaction with Glu, suggesting that enhanced detection of Glu by CPNs can be achieved by lowering the surface coordination of cobalt. Our results highlight the potential use of phosphate-based nanostructures as catalysts for electrochemical sensing of biochemical analytes.
2018
Pubblicato
Rilevanza internazionale
Articolo
Esperti anonimi
Settore CHIM/02 - CHIMICA FISICA
English
cobalt phosphate; density functional theory; glucose sensing; nanoflowers; non-enzymatic
Tomanin, P.p., Cherepanov, P.v., Besford, Q.a., Christofferson, A.j., Amodio, A., Mcconville, C.f., et al. (2018). Cobalt phosphate nanostructures for non-enzymatic glucose sensing at physiological pH. ACS APPLIED MATERIALS & INTERFACES, 10(49), 42786-42795 [10.1021/acsami.8b12966].
Tomanin, Pp; Cherepanov, Pv; Besford, Qa; Christofferson, Aj; Amodio, A; Mcconville, Cf; Yarovsky, I; Caruso, F; Cavalieri, F
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/215539
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