Abstract
We present a novel confocal microscope that has dual-axis architecture and biaxial postobjective scanning for the collection of fluorescence images from biological specimens. This design uses two low-numerical-aperture lenses to achieve high axial resolution and long working distance, and the scanning mirror located distal to the lenses rotates along the orthogonal axes to produce arc-surface images over a large field of view (FOV). With fiber optic coupling, this microscope can potentially be scaled down to millimeter dimensions via microelectromechanical systems (MEMS) technology. We demonstrate a benchtop prototype with a spatial resolution ≤4.4 μm that collects fluorescence images with a high SNR and a good contrast ratio from specimens expressing GFP. Furthermore, the scanning mechanism produces only small differences in aberrations over the image FOV. These results demonstrate proof of concept of the dual-axis confocal architecture for in vivo molecular and cellular imaging. © 2004 Society of Photo-Optical Instrumentation Engineers.
Cite
CITATION STYLE
Wang, T. D., Contag, C. H., Mandella, M. J., Chan, N. Y., & Kino, G. S. (2004). Confocal fluorescence microscope with dual-axis architecture and biaxial postobjective scanning. Journal of Biomedical Optics, 9(4), 735. https://doi.org/10.1117/1.1760760
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.