4.6 Article

Flexible and disposable gold nanoparticles-N-doped carbon-modified electrochemical sensor for simultaneous detection of dopamine and uric acid

Journal

NANOTECHNOLOGY
Volume 32, Issue 6, Pages -

Publisher

IOP PUBLISHING LTD
DOI: 10.1088/1361-6528/abc388

Keywords

gold nanoparticle; electrochemical sensor; uric acid; dopamine; flexible strip sensor

Funding

  1. National Natural Science Foundation of China [51502253, U1405226, 21503175, 21705135]
  2. Natural Science Foundation of Guangdong Province [2016A030310369]
  3. Natural Science Foundation of Fujian Province [2017J01104]
  4. Fundamental Research Funds for the Central Universities of China [20720160127, 20720180013]

Ask authors/readers for more resources

A gold nanoparticles-hosted mesoporous nitrogen-doped carbon matrix prepared using bovine serum albumin (BSA) exhibited effective, sensitive and selective properties in a flexible sensor system for simultaneous detection of uric acid and dopamine. The nanohybrid sensor showed excellent response towards both analytes, suggesting promising applications in the development of electrochemical biosensors.
Catalytic and electrocatalytic applications of supported metal nanoparticles are hindered due to an aggregation of metal nanoparticles and catalytic leaching under harsh operations. Hence, stable and leaching free catalysts with high surface area are extremely desirable but also challenging. Here we report a gold nanoparticles-hosted mesoporous nitrogen doped carbon matrix, which is prepared using bovine serum albumin (BSA) through calcination. BSA plays three roles in this process as a reducing agent, capping agent and carbon precursor, hence the protocol exhibits economic and sustainable. Gold nanoparticles at N-doped BSA carbon (AuNPs@NBSAC)-modified three-electrode strip-based flexible sensor system has been developed, which displayed effective, sensitive and selective for simultaneous detection of uric acid (UA) and dopamine (DA). The AuNPs@NBSAC-modified sensor showed an excellent response toward DA with a linear response throughout the concentration range from 1 to 50 mu M and a detection limit of 0.05 mu M. It also exhibited an excellent response toward UA, with a wide detection range from 5 to 200 mu M as well as a detection limit of 0.1 mu M. The findings suggest that the AuNPs@NBSAC nanohybrid reveals promising applications and can be considered as potential electrode materials for development of electrochemical biosensors.

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