Target-to-Background Separation for Spectral Unmixing in In-Vivo Fluorescence Imaging

We present a novel fluorescence spectral unmixing based on target-to-background separation pre- processing, which effectively separates the multi-target fluorescence from all background autofluorescence (BF) without any hardware-based BF acquisition and tissue specific BF estimation. Specifically, w...

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Published inShanghai jiao tong da xue xue bao Vol. 19; no. 5; pp. 600 - 611
Main Author 赵勇 胡程 彭金良 秦斌杰
Format Journal Article
LanguageEnglish
Published Heidelberg Shanghai Jiaotong University Press 2014
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Summary:We present a novel fluorescence spectral unmixing based on target-to-background separation pre- processing, which effectively separates the multi-target fluorescence from all background autofluorescence (BF) without any hardware-based BF acquisition and tissue specific BF estimation. Specifically, we first enhance the intrinsic accumulation contrast in target-to-background fluorescence using h-dome transformation; then separate multi-target fluorescence areas from the background in sparse multispectral data utilizing kernel maximum auto- correlation factor analysis; we further use fast marching-based image inpainting method to patch up the removed target fluorescence areas and reconstruct the multispectral BF; with the BF matrix being subtracted from the original data, the multi-target fluorophores are easily unmixed from the subtracted data using multivariate curve resolution-alternating least squares method. In two preliminary in-vivo experiments, the proposed method demon- strated excellent performance to unmix multi-target fluorescences while other state-of-art unmixing methods failed to get desired results.
Bibliography:fluorescence imaging, spectral unmixing, autofluorescence removal, target detection, kernel maxi-mum autocorrelation factor, target-to-background separation
31-1943/U
We present a novel fluorescence spectral unmixing based on target-to-background separation pre- processing, which effectively separates the multi-target fluorescence from all background autofluorescence (BF) without any hardware-based BF acquisition and tissue specific BF estimation. Specifically, we first enhance the intrinsic accumulation contrast in target-to-background fluorescence using h-dome transformation; then separate multi-target fluorescence areas from the background in sparse multispectral data utilizing kernel maximum auto- correlation factor analysis; we further use fast marching-based image inpainting method to patch up the removed target fluorescence areas and reconstruct the multispectral BF; with the BF matrix being subtracted from the original data, the multi-target fluorophores are easily unmixed from the subtracted data using multivariate curve resolution-alternating least squares method. In two preliminary in-vivo experiments, the proposed method demon- strated excellent performance to unmix multi-target fluorescences while other state-of-art unmixing methods failed to get desired results.
ZHAO Yong , HU Cheng , PENG Jin-liang, QIN Bin-jie (School of Biomedical Engineering, Shanghai Jiaotong University, Shanghai 200240, China)
ObjectType-Article-1
SourceType-Scholarly Journals-1
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content type line 23
ISSN:1007-1172
1995-8188
DOI:10.1007/s12204-014-1548-9