High-speed processing architecture for spectral-domain optical coherence microscopy

被引:8
作者
Chelliyil, Robin G. [1 ]
Ralston, Tyler S. [1 ]
Marks, Daniel L. [1 ]
Boppart, Stephen A. [1 ]
机构
[1] Univ Illinois, Dept Elect & Comp Engn, Biophoton Imaging Lab, Beckman Inst Adv Sci & Technol, Urbana, IL 61801 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
optical coherence tomography; optical coherence microscopy; en face image; numerical aperture;
D O I
10.1117/1.2960018
中图分类号
Q5 [生物化学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Optical coherence microscopy (OCM) is an interferometric technique that combines principles of confocal microscopy and optical coherence tomography (OCT) to obtain high-resolution en face images. Axial and lateral resolutions of several microns can be achieved using OCM depending on the numerical aperture (NA) of the objective and sample properties. We address the computational complexity that is inherent in spectral-domain OCM systems that limits its real-time capability as a microscope. An architecture that will improve the efficiency of the computation involved is presented. Currently, spectral-domain OCM images are obtained by individually taking the Fourier transform of each axial scan in cross-sectional frames and computationally slicing them to generate en face images. The real-time architecture presented here relies on the fact that only one Fourier domain point of a given axial scan needs to be computed rather than computing all the Fourier domain points, which can frequently require a significant amount of time to compute. This new realization has been shown to reduce the processing time to obtain the en face OCM images by a factor of 30. (C) 2008 Society of Photo-Optical Instrumentation Engineers.
引用
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页数:4
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