Spectral unmixing techniques for optoacoustic imaging of tissue pathophysiology

被引:61
|
作者
Tzoumas, Stratis
Ntziachristos, Vasilis [1 ,2 ,3 ]
机构
[1] Helmholtz Zentrum Munchen, IBMI, Neuherberg, Germany
[2] Tech Univ Munich, Chair Biol Imaging, Munich, Germany
[3] Tech Univ Munich, Lehrstuhl Biol Bildgebung, Ismaninger Str 22, D-81675 Munich, Germany
基金
欧洲研究理事会;
关键词
multispectral optoacoustic imaging; spectroscopic photoacoustic imaging; spectral unmixing; TOMOGRAPHY; INVERSION; DEEP;
D O I
10.1098/rsta.2017.0262
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
A key feature of optoacoustic imaging is the ability to illuminate tissue at multiple wavelengths and therefore record images with a spectral dimension. While optoacoustic images at single wavelengths reveal morphological features, in analogy to ultrasound imaging or X-ray imaging, spectral imaging concedes sensing of intrinsic chromophores and externally administered agents that can reveal physiological, cellular and subcellular functions. Nevertheless, identification of spectral moieties within images obtained at multiple wavelengths requires spectral unmixing techniques, which present a unique mathematical problem given the three-dimensional nature of the optoacoustic images. Herein we discuss progress with spectral unmixing techniques developed for multispectral optoacoustic tomography. We explain how different techniques are required for accurate sensing of intrinsic tissue chromophores such as oxygenated and deoxygenated haemoglobin versus extrinsically administered photo-absorbing agents and nanoparticles. Finally, we review recent developments that allow accurate quantification of blood oxygen saturation (sO(2)) by transforming and solving the sO(2) estimation problem from the spatial to the spectral domain. This article is part of the themed issue 'Challenges for chemistry in molecular imaging'.
引用
收藏
页数:9
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