
Proceedings Paper
Confocal reflectance theta line-scanner for imaging tissues in vivoFormat | Member Price | Non-Member Price |
---|---|---|
$17.00 | $21.00 |
Paper Abstract
A confocal reflectance theta line-scanner is being developed for imaging human tissues in vivo. The theta line scanner design potentially offers a newer alternative to current point scanners that may simplify the optics, electronics and mechanics and lead to smaller, inexpensive confocal microscopes. An oscillating galvanometric mirror directly scans in the pupil of a cylindrical lens and one-half of an objective lens, to produce a focused, scanned line in the object plane within tissue. Backscattered light is collected by the other half of the objective lens and focused onto a linear CMOS detector. The illumination is with a diode laser at 830 nm and imaging with a 10X, 0.8 NA water immersion lens. The illumination and detection paths are thus oriented at an angle (theta) to each other, and are separate everywhere except in the confocal plane. This configuration eliminates back-scattered light from optical components and enhances contrast. Optical design analysis has been verified with experimental results, demonstrating lateral resolution on the order of 1 um and optical sectioning (axial resolution) better than 5 um within living human skin. A Fourier optics-based analytical model is in progress to evaluate line spread functions versus illumination and detection pupil conditions. Nuclear and cellular detail is imaged in the epidermis of human skin in vivo and ex vivo (freshly excised specimens). Such a scanner may prove useful for imaging human tissues in clinical and intra-operative settings.
Paper Details
Date Published: 24 March 2005
PDF: 6 pages
Proc. SPIE 5701, Three-Dimensional and Multidimensional Microscopy: Image Acquisition and Processing XII, (24 March 2005); doi: 10.1117/12.584387
Published in SPIE Proceedings Vol. 5701:
Three-Dimensional and Multidimensional Microscopy: Image Acquisition and Processing XII
Jose-Angel Conchello; Carol J. Cogswell; Tony Wilson, Editor(s)
PDF: 6 pages
Proc. SPIE 5701, Three-Dimensional and Multidimensional Microscopy: Image Acquisition and Processing XII, (24 March 2005); doi: 10.1117/12.584387
Show Author Affiliations
Peter J. Dwyer, Northeastern Univ. (United States)
CenSISS, Northeastern Univ. (United States)
Charles A. DiMarzio, Northeastern Univ. (United States)
CenSISS, Northeastern Univ. (United States)
William J. Fox, Lucid, Inc. (United States)
CenSISS, Northeastern Univ. (United States)
Charles A. DiMarzio, Northeastern Univ. (United States)
CenSISS, Northeastern Univ. (United States)
William J. Fox, Lucid, Inc. (United States)
James M. Zavislan, The Institute of Optics/Univ. of Rochester (United States)
Milind Rajadhyaksha, CenSISS, Northeastern Univ. (United States)
Memorial Sloan Kettering Cancer Ctr. (United States)
Milind Rajadhyaksha, CenSISS, Northeastern Univ. (United States)
Memorial Sloan Kettering Cancer Ctr. (United States)
Published in SPIE Proceedings Vol. 5701:
Three-Dimensional and Multidimensional Microscopy: Image Acquisition and Processing XII
Jose-Angel Conchello; Carol J. Cogswell; Tony Wilson, Editor(s)
© SPIE. Terms of Use
