Enzyme Immobilization by Inkjet Printing on Reagentless Biosensors for Electrochemical Phosphate Detection

Biosensors (Basel). 2024 Mar 30;14(4):168. doi: 10.3390/bios14040168.

Abstract

Enzyme-based biosensors commonly utilize the drop-casting method for their surface modification. However, the drawbacks of this technique, such as low reproducibility, coffee ring effects, and challenges in mass production, hinder its application. To overcome these limitations, we propose a novel surface functionalization strategy of enzyme crosslinking via inkjet printing for reagentless enzyme-based biosensors. This method includes printing three functional layers onto a screen-printed electrode: the enzyme layer, crosslinking layer, and protective layer. Nanomaterials and substrates are preloaded together during our inkjet printing. Inkjet-printed electrodes feature a uniform enzyme deposition, ensuring high reproducibility and superior electrochemical performance compared to traditional drop-casted ones. The resultant biosensors display high sensitivity, as well as a broad linear response in the physiological range of the serum phosphate. This enzyme crosslinking method has the potential to extend into various enzyme-based biosensors through altering functional layer components.

Keywords: enzyme immobilization; inkjet printing; phosphate detection; reagentless biosensor; screen-printed electrode.

MeSH terms

  • Biosensing Techniques*
  • Electrochemical Techniques*
  • Electrodes
  • Enzymes, Immobilized* / chemistry
  • Phosphates*
  • Printing
  • Reproducibility of Results

Substances

  • Enzymes, Immobilized
  • Phosphates