4.7 Article

Disposable Polymeric Nanostructured Plasmonic Biosensors for Cell Culture Adhesion Monitoring

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fbioe.2021.799325

关键词

plasmonic nanostructures; cell confluency; cell culture; nanocrystals; optical biosensor

资金

  1. European Research Council program [714317]
  2. European Commission under FET-open program BLOC project [GA-863037]
  3. Spanish Ministry of Economy and Competitiveness, through the Severo Ochoa Program for Centres of Excellence in RD [SEV-2016-2019]
  4. CERCA Programme/Generalitat de Catalunya [2017-SGR-1079]
  5. Fundacion Bancaria la Caixa-Obra Social la Caixa
  6. European Research Council (ERC) [714317] Funding Source: European Research Council (ERC)

向作者/读者索取更多资源

Optical biosensors based on plasmonic nanomaterials have attracted significant scientific interest for their sensitivity, directness, and potential for multiplexing. A pilot study was conducted using optical discs as nanotemplates to develop an integrated plasmonic biosensor for monitoring cell adhesion and growth, showing promising results for real-time analysis of living cells behavior and culture conditions. This approach could offer a non-destructive and reliable tool for assessing cell viability and growth with low variability between technical replicates, improving experimental replicability.
Over the last years, optical biosensors based on plasmonic nanomaterials have gained great scientific interest due to their unquestionable advantages compared to other biosensing technologies. They can achieve sensitive, direct, and label-free analysis with exceptional potential for multiplexing and miniaturization. Recently, it has been demonstrated the potential of using optical discs as high throughput nanotemplates for the development of plasmonic biosensors in a cost-effective way. This work is a pilot study focused on the development of an integrated plasmonic biosensor for the monitoring of cell adhesion and growth of human retinal pigmented cell line (ARPE-19) under different media conditions (0 and 2% of FBS). We observed an increase of the plasmonic band displacement under 2% FBS compared to 0% conditions over time (1, 3, and 5 h). These preliminary results show that the proposed plasmonic biosensing approach is a direct, non-destructive, and real-time tool that could be employed in the study of living cells behavior and culture conditions. Furthermore, this setup could assess the viability of the cells and their growth over time with low variability between the technical replicates improving the experimental replicability.

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