4.5 Article

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

期刊

JOURNAL OF BIOMEDICAL OPTICS
卷 9, 期 4, 页码 735-742

出版社

SPIE-INT SOCIETY OPTICAL ENGINEERING
DOI: 10.1117/1.1760760

关键词

confocal; microscope; fluorescence; molecular biology; imaging; in vivo

资金

  1. NCI NIH HHS [CA92862, R24 CA092862, CA88303, CA86312] Funding Source: Medline
  2. NIDDK NIH HHS [K08 DK067618-05, K08 DK067618-04, T32 DK007056, K08 DK067618, T32DK07056-27] Funding Source: Medline
  3. NIGMS NIH HHS [1 R43 GM64028-01] Funding Source: Medline

向作者/读者索取更多资源

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.

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