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Published February 19, 2013 | Accepted Version + Supplemental Material
Journal Article Open

Wide Field-of-View On-Chip Talbot Fluorescence Microscopy for Longitudinal Cell Culture Monitoring from within the Incubator

Abstract

Time-lapse or longitudinal fluorescence microscopy is broadly used in cell biology. However, current available time-lapse fluorescence microscopy systems are bulky and costly. The limited field-of-view (FOV) associated with the microscope objective necessitates mechanical scanning if a larger FOV is required. Here we demonstrate a wide FOV time-lapse fluorescence self-imaging Petri dish system, termed the Talbot Fluorescence ePetri, which addresses these issues. This system's imaging is accomplished through the use of the Fluorescence Talbot Microscopy (FTM). By incorporating a microfluidic perfusion subsystem onto the platform, we can image cell cultures directly from within an incubator. Our prototype has a resolution limit of 1.2 μm and an FOV of 13 mm^2. As demonstration, we obtained time-lapse images of HeLa cells expressing H2B-eGFP. We also employed the system to analyze the cells' dynamic response to an anticancer drug, camptothecin (CPT). This method can provide a compact and simple solution for automated fluorescence imaging of cell cultures in incubators.

Additional Information

© 2013 American Chemical Society. Received: November 20, 2012. Accepted: January 28, 2013. Published: January 28, 2013. We thank Dr. Scott Fraser (Biological Imaging Center, Caltech) for use of his lab facilities. This project is funded by National Institute of Health under Grant No. 1R01AI096226-01. D.V.B. is supported by NHLBI NRSA fellowship F30 HL110723.

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Accepted Version - nihms441559.pdf

Supplemental Material - ac303356v_si_001.pdf

Supplemental Material - ac303356v_si_002.avi

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August 19, 2023
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