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Absorption-Based Hyperspectral Imaging and Analysis of Single Erythrocytes

机译:基于吸收的高光谱成像和单红细胞分析

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We report an absorption-based hyperspectral imaging and analysis technique to resolve unique physicochemical characteristics of subcellular substances in single erythrocytes. We constructed a microscope system installed with a spectral light engine capable of controlling the spectral shape of the illumination light by a digital micromirror device. The hyperspectral imaging system and the sequential maximum angle convex cone algorithm allow us to extract unique spectral signatures (i.e., endmembers) for different types of hemoglobin, such as oxyhemoglobin, methemoglobin, and hemozoin, and scatter from cell membrane in single erythrocytes. Further statistical endmember analysis, conducted on the hyperspectral image data, provides the abundances of specific endmembers, which can be used to build intracellular maps of the distribution of substances of interest. In addition, we perform modeling based on Mie theory to explain the scattering signatures as a function of scattering angle. The developed imaging and analysis technique enables label-free molecular imaging of endogenous biomarkers in single erythrocytes in order to build oxymetric standards on a cellular level and ultimately for in vivo as well.
机译:我们报告了基于吸收的高光谱成像和分析技术,以解决单个红细胞中亚细胞物质的独特理化特征。我们构建了一个装有光谱光引擎的显微镜系统,该光谱光引擎能够通过数字微镜设备控制照明光的光谱形状。高光谱成像系统和顺序最大角度凸锥算法使我们能够提取不同类型的血红蛋白(例如氧合血红蛋白,高铁血红蛋白和血红蛋白)的独特光谱特征(即末端成员),并从单个红细胞的细胞膜中散射出来。在高光谱图像数据上进行的进一步统计端成员分析提供了特定端成员的丰度,可用于构建目标物质分布的细胞内图。此外,我们基于米氏理论进行建模,以解释散射特征与散射角的关系。发达的成像和分析技术可对单个红细胞中的内源性生物标志物进行无标记分子成像,从而在细胞水平上最终在体内也建立血氧定量标准。

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