Share Email Print
cover

Proceedings Paper

An achromatized endoscope for ultrahigh-resolution optical coherence tomography
Format Member Price Non-Member Price
PDF $14.40 $18.00
cover GOOD NEWS! Your organization subscribes to the SPIE Digital Library. You may be able to download this paper for free. Check Access

Paper Abstract

Mouse models are increasingly important for studying human GI pathology. OCT provides minimally invasive, cross-sectional images that indicate the thickness and scattering density of underlying tissue. We have developed endoscopic ultrahigh resolution OCT (UHR-OCT) to imaging mouse colon in vivo. The reduced scale of the mouse colon makes tissue light penetration much less problematic, and high resolution acutely necessary. Higher lateral resolution requires a departure from the traditional cemented GRIN lens design. We support the need for better chromatic aberration than can be achieved by a GRIN lens using commercial raytracing software. We have designed and built a 2mm diameter endoscopic UHR-OCT system achromatized for 770-1020nm for use with a Titanium:sapphire laser with 260 nm bandwidth at full-width-half-maximum centered at 800 nm while achieving a 4.4um lateral spot dimension at focus. A pair of KZFSN5/SFPL53 doublets provides excellent primary and secondary color correction to maintain wide bandwidth through the imaging depth. A slight deviation from normal beam exit angle suppresses collection of the strong back reflection at the exit window surface. The novel design endoscope was built and characterized for through focus bandwidth, axial resolution, signal to noise, and lateral spot dimension. Performance is demonstrated on in vivo mouse colon. Ultrahigh-resolution images of mouse tissue enable the visualization of microscopic features, including crypts that have previously been observed with standard resolution OCT in humans but were too small to see in mouse tissue. Resolution near the cellular level is potentially capable of identifying abnormal crypt formation and dysplastic cellular organization.

Paper Details

Date Published: 7 October 2005
PDF: 7 pages
Proc. SPIE 5861, Optical Coherence Tomography and Coherence Techniques II, 586110 (7 October 2005); doi: 10.1117/12.632994
Show Author Affiliations
Alexandre R. Tumlinson, The Univ. of Arizona (United States)
Jennifer K. Barton, The Univ. of Arizona (United States)
James McNally, Optical Sciences Ctr., The Univ. of Arizona (United States)
Angelika Unterhuber, Medical Univ. of Vienna (Austria)
Boris Hermann, Medical Univ. of Vienna (Austria)
Harald Sattmann, Medical Univ. of Vienna (Austria)
Wolfgang Drexler, Medical Univ. of Vienna (Austria)


Published in SPIE Proceedings Vol. 5861:
Optical Coherence Tomography and Coherence Techniques II
Wolfgang Drexler, Editor(s)

© SPIE. Terms of Use
Back to Top