Hyperspectral imaging: A novel approach for microscopic analysis

被引:0
|
作者
Schultz, RA
Nielsen, T
Zavaleta, JR
Ruch, R
Wyatt, R
Garner, HR
机构
[1] Univ Texas, SW Med Ctr, McDermott Ctr Human Growth & Dev, Dallas, TX 75235 USA
[2] Univ Texas, SW Med Ctr, Dept Pathol, Dallas, TX USA
[3] Univ Texas, SW Med Ctr, Dept Biochem, Dallas, TX 75235 USA
[4] Univ Texas, SW Med Ctr, Dept Internal Med, Dallas, TX USA
[5] Univ Texas, SW Med Ctr, Ctr Biomed Invent, Dallas, TX USA
来源
CYTOMETRY | 2001年 / 43卷 / 04期
关键词
light microscopy; hyperspectral imaging; fluorescence; emission spectrum; image analysis;
D O I
10.1002/1097-0320(20010401)43:4<239::AID-CYTO1056>3.0.CO;2-Z
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Background: The usefulness of the light microscope has been dramatically enhanced by recent developments in hardware and software. However, current technologies lack the ability to capture and analyze a high-resolution image representing a broad diversity of spectral signatures in a single-pass view. We show that hyperspectral imaging offers such a technology. Methods and Results: We developed a prototype hyperspectral imaging microscope capable of collecting the complete emission spectrum from a microscope slide. A standard epifluorescence microscope was optically coupled to an imaging spectrograph. with output recorded by a CCD camera. Software was developed for image acquisition and computer display of resultant X-Y images with spectral information. Individual images were captured representing Y-wavelength planes, with the stage successively moved in the X direction, allowing an image cube to be constructed from the compilation of generated scan files. This prototype instrument was tested with samples relevant to cytogenetic, histologic, cell fusion, microarray scanning, and materials science applications. Conclusions: Hyperspectral imaging microscopy permits the capture and identification of different spectral signatures present in an optical field during a single-pass evaluation, including molecules with overlapping but distinct emission spectra. This instrument can reduce dependence on custom optical filters and, in future imaging applications, should facilitate the use of new fluorophores or the simultaneous use of similar fluorophores. Cytometry 43:239-247, 2001. (C) Wiley-Liss, Inc.
引用
收藏
页码:239 / 247
页数:9
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