Development of microfluidic devices for in situ investigation of cells using surface-enhanced Raman spectroscopy
(Conference Presentation)

Yu-Han Ho; Daniel D. Galvan; Qiuming Yu

doi:10.1117/12.2213302

26 April 2016 Development of microfluidic devices for in situ investigation of cells using surface-enhanced Raman spectroscopy (Conference Presentation)

Yu-Han Ho, Daniel D. Galvan, Qiuming Yu

Author Affiliations +

Proceedings Volume 9705, Microfluidics, BioMEMS, and Medical Microsystems XIV; 97050R (2016) https://doi.org/10.1117/12.2213302
Event: SPIE BiOS, 2016, San Francisco, California, United States

Abstract

Surface-enhanced Raman spectroscopy (SERS) has immerged as a power analytical and sensing technique for many applications in biomedical diagnosis, life sciences, food safety, and environment monitoring because of its molecular specificity and high sensitivity. The inactive Raman scattering of water molecule makes SERS a suitable tool for studying biological systems. Microfluidic devices have also attracted a tremendous interest for the aforementioned applications. By integrating SERS-active substrates with microfluidic devices, it offers a new capability for in situ investigation of biological systems, their dynamic behaviors, and response to drugs or microenvironment changes. In this work, we designed and fabricated a microfluidic device with SERS-active substrates surrounding by cell traps in microfluidic channels for in situ study of live cells using SERS. The SERS-active substrates are quasi-3D plasmonic nanostructure array (Q3D-PNA) made in h-PDMS/PMDS with physically separated gold film with nanoholes op top and gold nanodisks at the bottom of nanowells. 3D finite-difference time-domain (3D-FDTD) electromagnetic simulations were performed to design Q3D-PNAs with the strongest local electric fields (hot spots) at the top or bottom water/Au interfaces for sensitive analysis of cells and small components, respectively. The Q3D-PNAs with the hot spots on top and bottom were placed at the up and down stream of the microfluidic channel, respectively. Each Q3D-PNA pattern was surrounded with cell trapping structures. The microfluidic device was fabricated via soft lithography. We demonstrated that normal (COS-7) and cancer (HpeG2) cells were captured on the Q3D-PNAs and investigated in situ using SERS.

Conference Presentation

Citation Download Citation

Yu-Han Ho, Daniel D. Galvan, and Qiuming Yu "Development of microfluidic devices for in situ investigation of cells using surface-enhanced Raman spectroscopy (Conference Presentation)", Proc. SPIE 9705, Microfluidics, BioMEMS, and Medical Microsystems XIV, 97050R (26 April 2016); https://doi.org/10.1117/12.2213302

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