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Enhanced Peroxidase-Like Activity of Platinum Nanoparticles Decorated on Nickel- and Nitrogen-Doped Graphene Nanotubes: Colorimetric Detection of Glucose Publisher Pubmed



Fakhri N1 ; Salehnia F2 ; Mohammad Beigi S2 ; Aghabalazadeh S3 ; Hosseini M4 ; Ganjali MR2, 5
Authors
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Authors Affiliations
  1. 1. School of Chemical Engineering, College of engineering, University of Tehran, Tehran, 1417614418, Iran
  2. 2. Center of Excellence in Electrochemistry, Faculty of Chemistry, University of Tehran, Tehran, 1417614418, Iran
  3. 3. CinnaGen Medical Biotechnology Research Center, Alborz University of Medical Sciences, Karaj, 1467635165, Iran
  4. 4. Department of Life Science Engineering, Faculty of New Sciences & Technologies, University of Tehran, Tehran, 1417614418, Iran
  5. 5. Biosensor Research Center, Endocrinology and Metabolism Molecular-Cellular Sciences Institute, Tehran University of Medical Sciences, Tehran, 1417614418, Iran

Source: Microchimica Acta Published:2019


Abstract

A nanostructured catalyst is introduced that demonstrates peroxidase mimicking activity. It consists of nickel- and nitrogen-doped graphene nanotubes loaded with platinum nanoparticles. Pt-decorated Ni-doped nitrogen-rich graphitic nanotube (Pt/Ni@NGT) was synthesized using a two-step procedure in which the precursors were first refluxed to form a supramolecular assembly followed by a pyrolysis and leaching step to form nanotubes. Afterwards, Pt was decorated on the outer surface of nanotube by an ultrasound assisted method. Pt/Ni@NGT was characterized by XPS, TEM, SEM, and HAADF–STEM. The as-prepared Pt/Ni@NGT nanostructure was used for the detection of glucose via catalyzing the oxidation of a substrate, 3,3′,5,5′-tetramethylbenzidine (TMB), to form a blue product (ox-TMB), thereby enabling colorimetric assay for enzymatically generated H2O2. The nanostructure exhibited excellent biocompatibility and led to highly efficient immobilization and retention of GOx. The method has a linear response in the 43 pM to 220 μM glucose concentration range, a detection limit as low as 1 pM and a limit of quantification of 3.4pM, along with good reproducibility(< 3%). A paper based visual microfluidic assay was also worked out that has an analytical range that extends from 0.1–50 mM. It is simple and rapid enough to be useful as a glucose home test. The method was successfully applied to the determination of glucose in tear and saliva samples. [Figure not available: see fulltext.]. © 2019, Springer-Verlag GmbH Austria, part of Springer Nature.
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