4.6 Article

Integrated multi-material portable 3D-printed platform for electrochemical detection of dopamine and glucose

Journal

ANALYST
Volume 147, Issue 20, Pages 4598-4606

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d2an00862a

Keywords

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Funding

  1. Scottish Enterprise
  2. Scottish Funding Council GCRF
  3. EngD Medical Devices CDT by the EPSRC CDT in Biomedical Devices and Health Technologies [EP/L015595/1]

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3D printing has become an important tool in many research areas, including biosensing. By using multi-material 3D printing technology, we have successfully produced a compact electrochemical sensor that can operate efficiently with only 100 μL of sample. We tested the performance and sensitivity of the sensor, and investigated the influence of print orientation and thickness on its electrochemical performance.
3D-printing has become a fundamental part of research in many areas of investigation since it provides rapid and personalized production of parts that meet very specific user needs. Biosensing is not an exception, and production of electrochemical sensors that can detect a variety of redox mediators and biologically relevant molecules has been widely reported. However, most 3D-printed electrochemical sensors detailed in the literature rely on big, individual, single-material electrodes that require large sample volumes to perform effectively. Our work exploits multi-material fused filament fabrication 3D-printing to produce a compact electrochemical sensor able to operate with only 100 mu L of sample. We report cyclic voltammetry, differential pulse voltammetry, and chronoamperometry results to assess sensor performance and sensitivity. We investigated the influence of layer print orientation and layer thickness on the electrochemical performance of the sensor, and used the optimal parameters to produce the final device. The integrated 3D-printed platform successfully detects electrochemical activity for hexaammineruthenium(iii) chloride and potassium ferricyanide (0.1 mM to 2 mM in 100 mM KCl), dopamine (50 mu M to 1 mM in 1xPBS), and glucose via mediated amperometric glucose oxidase enzyme-based sensing (1 mM to 12 mM in 1xPBS), indicating good acceptance of biological modification. These results reveal the exciting potential of multi-material 3D-printing and how it can be used for the rapid development of efficient, small, integrated, personalized electrochemical biosensors.

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