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Wavelength-scanning surface plasmon resonance microscopy: A novel tool for real time sensing of cell-substrate interactions
This paper, for the first time, presents a wavelength-scanning surface plasmon resonance microscope (WS-SPRM) as a label-free biosensor capable of measuring cell-substrate interaction. The approach utilized a liquid crystal tunable filter (LCTF) as a fast and flexible wavelength-scanning device that...
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Published in: | Biosensors & bioelectronics 2019-12, Vol.145, p.111717-111717, Article 111717 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | This paper, for the first time, presents a wavelength-scanning surface plasmon resonance microscope (WS-SPRM) as a label-free biosensor capable of measuring cell-substrate interaction. The approach utilized a liquid crystal tunable filter (LCTF) as a fast and flexible wavelength-scanning device that can implement a wavelength-scanning and SPR imaging cycle within 1 s. The system was verified by monitoring the dynamics of cellular processes including cell detachment and electroporation of individual cells. It was found that the WS-SPRM presented better performance than the intensity-based SPRM (I-SPRM) in the imaging of cell adhesion. The results also indicated that the WS-SPRM exhibited a larger dynamic range in monitoring cell electroporation than that of I-SPRM. In summary, the developed WS-SPRM in this study provides a promising technique for real-time monitoring of cell-substrate interaction.
•For the first time, a wavelength-scanning SPRM is developed as a label-free biosensor to measure cell-substrate interaction.•The WS-SPRM has been exploited to monitor the dynamics of cellular processes including detachment and electroporation.•The WS-SPRM exhibits larger dynamic range compared to the intensity SPRM, which is beneficial for the cell adhesion imaging. |
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ISSN: | 0956-5663 1873-4235 |
DOI: | 10.1016/j.bios.2019.111717 |