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首页> 外文期刊>IEEE Transactions on Medical Imaging >Unmixing Molecular Agents From Absorbing Tissue in Multispectral Optoacoustic Tomography
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Unmixing Molecular Agents From Absorbing Tissue in Multispectral Optoacoustic Tomography

机译:在多光谱光声层析成像中从吸收组织中分离分子试剂

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摘要

Detection of intrinsic or extrinsically administered chromophores and photo-absorbing nanoparticles has been achieved by multi-spectral optoacoustic tomography (MSOT). The detection sensitivity of MSOT depends not only on the signal to noise ratio considerations, as in conventional optoacoustic (photoacoustic) tomography implementations, but also on the ability to resolve the molecular targets of interest from the absorbing tissue background by means of spectral unmixing or sub-pixel detection methods. However, it is not known which unmixing methods are optimally suited for the characteristics of multispectral optoacoustic images. In this work we investigated the performance of different sub-pixel detection methods, typically used in remote sensing hyperspectral imaging, within the context of MSOT. A quantitative comparison of the different algorithmic approaches was carried out in an effort to identify methods that operate optimally under the particulars of molecular imaging applications. We find that statistical sub-pixel detection methods can demonstrate a unique detection performance with up to five times enhanced sensitivity as compared to linear unmixing approximations, under the condition that the optical agent of interest is sparsely present within the tissue volume, as common when using targeted agents and reporter genes.
机译:通过多光谱光声层析成像(MSOT)已经实现了对内在或外在发色团和光吸收纳米粒子的检测。 MSOT的检测灵敏度不仅取决于像常规光声(光声)层析成像实施中的信噪比考虑因素,而且还取决于通过光谱解混或亚光谱从吸收的组织背景中分离感兴趣的分子靶标的能力-像素检测方法。然而,未知哪种解混方法最适合于多光谱光声图像的特性。在这项工作中,我们研究了在MSOT背景下通常用于遥感高光谱成像中的不同子像素检测方法的性能。为了确定在分子成像应用程序的特殊情况下可以最佳运行的方法,对不同的算法方法进行了定量比较。我们发现,在感兴趣的光学试剂稀疏地存在于组织体积内的情况下,统计亚像素检测方法可以证明独特的检测性能,与线性解混近似相比,灵敏度提高了五倍,这在使用时很常见。靶向剂和报道基因。

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