| Literature DB >> 15250760 |
Thomas D Wang1, Christopher H Contag, Michael J Mandella, Ning Y Chan, Gordon S Kino.
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 < or =4.4 microm 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.Mesh:
Year: 2004 PMID: 15250760 PMCID: PMC2093952 DOI: 10.1117/1.1760760
Source DB: PubMed Journal: J Biomed Opt ISSN: 1083-3668 Impact factor: 3.170