Abstract
Here, we report on the design, fabrication, and verification of a novel CMOS-imager-based contact imaging system. We acquired fluorescent images from live neurons by monitoring calcium changes with Fura-2 dye. Our current device consists of a removable absorption filter interfaced with a CMOS imaging sensor and an external DG-4 lamp for excitation. Fura-2 loaded Lymnaea stagnalis neurons were stimulated with dual excitation wavelengths of 340 and 380 nm; our image sensor detected 510-nm emission. We show that our system is capable of detecting intracellular calcium changes in Fura-2 loaded neurons. Further, this sensor also enabled viewing of multiple neurons over a large surface area simultaneously, an option that is not readily available in conventional light microscopy.
Author supplied keywords
Cite
CITATION STYLE
Mudraboyina, A. K., Blockstein, L., Luk, C. C., Syed, N. I., & Yadid-Pecht, O. (2014). A Novel Lensless Miniature Contact Imaging System for Monitoring Calcium Changes in Live Neurons. IEEE Photonics Journal, 6(1). https://doi.org/10.1109/JPHOT.2014.2304554
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.