Cytotoxicity assessment of MDA-MB-231 breast cancer cells on screen-printed graphene-carbon paste substrate

U Waiwijit1, W Kandhavivorn2, B Oonkhanond2

  • 1Nanoelectronics and MEMS Laboratory, National Electronics and Computer Technology Center, 112 Thailand Science Park, Phahon Yothin Road, Klong 1, Klong Luang, Pathumthani 12120, Thailand.

Insights

Graphene-carbon paste substrates show improved biocompatibility with MDA-MB-231 breast cancer cells at low graphene concentrations. This enhances cell viability and adhesion, suggesting potential for bio-electrochemical applications.

Area of Science:

  • Biomaterials Science
  • Nanotechnology
  • Cell Biology

Background:

  • Graphene's unique properties, including high electrical conductivity and electrocatalytic activity, make it promising for bio-electrochemical applications.
  • Limited understanding of graphene's biocompatibility with biological entities has hindered its widespread use in biological fields.
  • Assessing the cytotoxicity of graphene-based materials is crucial for developing safe and effective biomedical devices.

Purpose of the Study:

  • To evaluate the cytotoxic effects of graphene-carbon paste (GCP) substrates with varying graphene content on MDA-MB-231 breast cancer cells (MDA cells).
  • To determine the optimal graphene concentration for enhancing the biocompatibility of carbon paste electrodes for cell studies.
  • To investigate the impact of graphene on cell viability, adhesion, reactive oxygen species (ROS) production, and cell confluence.

Main Methods:

  • Graphene-carbon paste (GCP) substrates were prepared with different weight percentages (wt%) of graphene powder mixed into carbon paste.
  • Cytotoxicity was assessed through cell viability assays, cell adhesion studies, reactive oxygen species (ROS) production measurements, and Hoechst 33342 fluorescence staining.
  • MDA-MB-231 breast cancer cells were cultured on both carbon paste (CP) and GCP substrates over time.

Main Results:

  • Cell viability and adhesion on GCP substrates initially increased with graphene content up to 2.5 wt% before decreasing at higher concentrations.
  • Cell viability decreased over time on all substrates, but lower graphene concentrations mitigated this effect.
  • ROS production, induced by the carbon substrate, decreased with the inclusion of low graphene content, indicating reduced cytotoxicity.
  • Cell confluence, assessed by fluorescence staining, was enhanced on substrates with low graphene concentrations.

Conclusions:

  • Low-content graphene incorporation (up to 2.5 wt%) significantly improves the biocompatibility of carbon paste materials with MDA-MB-231 breast cancer cells.
  • Optimized graphene-carbon paste substrates demonstrate reduced cytotoxicity and enhanced cell adhesion and confluence.
  • These findings support the potential of graphene-modified carbon paste as an effective electrode material for electrochemical studies involving cancer cells.

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