Confocal fluorescence microscope with dual-axis architecture and biaxial postobjective scanning

被引:29
作者
Wang, TD
Contag, CH
Mandella, MJ
Chan, NY
Kino, GS
机构
[1] Stanford Univ, Sch Med, Stanford, CA 94305 USA
[2] Opt Biopsy Technol Inc, Palo Alto, CA 94301 USA
[3] Stanford Univ, Edward L Ginzton Lab, Stanford, CA 94305 USA
关键词
confocal; microscope; fluorescence; molecular biology; imaging; in vivo;
D O I
10.1117/1.1760760
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We present a novel confocal microscope that has dual-axis architecture and biaxial postobjective scanning for the collection 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 less than or equal to4.4 mum that collects fluorescence images with a high SNR and a good contrast ratio from specimens expressing GFR Furthermore, the scanning mechanism produces only small differences in aberrations over the image FOV. These results demonstrate proof of concept of the dualaxis confocal architecture for in vivo molecular and cellular imaging. (C) 2004 Society of Photo-Optical Instrumentation Engineers.
引用
收藏
页码:735 / 742
页数:8
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