Self-Calibrating On-Chip Localized Surface Plasmon Resonance Sensing for Quantitative and Multiplexed Detection of Cancer Markers in Human Serum.
Ozlem YavasSrdjan S AćimovićJose Garcia-GuiradoJohann BerthelotPaulina DoboszVanesa SanzRomain QuidantPublished in: ACS sensors (2018)
The need for point-of-care devices able to detect diseases early and monitor their status, out of a lab environment, has stimulated the development of compact biosensing configurations. Whereas localized surface plasmon resonance (LSPR) sensing integrated into a state-of-the-art microfluidic chip stands as a promising approach to meet this demand, its implementation into an operating sensing platform capable of quantitatively detecting a set of molecular biomarkers in an unknown biological sample is only in its infancy. Here, we present an on-chip LSPR sensor capable of performing automatic, quantitative, and multiplexed screening of biomarkers. We demonstrate its versatility by programming it to detect and quantify in human serum four relevant human serum protein markers associated with breast cancer.
Keyphrases
- high throughput
- circulating tumor cells
- single cell
- label free
- healthcare
- papillary thyroid
- primary care
- machine learning
- squamous cell
- quality improvement
- protein protein
- body mass index
- loop mediated isothermal amplification
- binding protein
- small molecule
- weight gain
- young adults
- physical activity
- amino acid
- weight loss