Department of Chemical Engineering, Imperial College London, South Kensington Campus, London SW7 2AZ, UK.
Analyst. 2019 Apr 23;144(9):2954-2964. doi: 10.1039/c8an01929k.
The depth of penetration and effective thickness in ATR-FTIR spectroscopic imaging are dependent on the wavelength and angle of incidence of the incoming light beam. We have demonstrated, for the first time, that variable angle micro ATR-FTIR, which is created via the insertion of circular apertures, is intrinsic at examining embedded components within a prostate tissue specimen. This is done by constructing a 3D model from the stacks of 2D chemical images obtained, each of which represents the spatial distribution of a chosen spectral band assigned to the component of interest at a different probing depth. ATR-FTIR imaging is also shown to have the ability to resolve subcellular components of cells such as organelles. For differentiation of diseased and non-diseased tissues, statistical tests are employed to analyse the spectral datasets obtained. When the second derivative of the spectral datasets was subjected to t-test analysis, the spectral differences between both samples in the fingerprint region are shown to be more significant at a shallow depth of penetration, with the greatest variance at the spectral band of 1235 cm-1 (vasPO2-), depicted by plotting the scores of PCA on its first two PCs. Overall, this paper demonstrates a non-destructive, label-free approach for examining heterogeneous biological samples in the z-direction to construct a 3D model using micro ATR-FTIR imaging, in a qualitative and semi-quantitative manner.
ATR-FTIR 光谱成像的穿透深度和有效厚度取决于入射光束的波长和入射角。我们首次证明,通过插入圆形光阑创建的可变角度微 ATR-FTIR 可以固有地检查前列腺组织标本内的嵌入式组件。这是通过从获得的二维化学图像堆栈构建 3D 模型来完成的,每个图像代表在不同探测深度处分配给感兴趣组件的选定光谱带的空间分布。ATR-FTIR 成像还显示出能够解析细胞的亚细胞成分,如细胞器。为了区分病变和非病变组织,我们采用统计检验来分析获得的光谱数据集。当对光谱数据集的二阶导数进行 t 检验分析时,在较浅的穿透深度下,指纹区域中两个样本之间的光谱差异显示出更显著的差异,在 1235cm-1 的光谱带(vasPO2-)处具有最大的方差,这是通过绘制 PCA 在其前两个 PC 上的得分来表示的。总的来说,本文展示了一种非破坏性、无标记的方法,用于使用微 ATR-FTIR 成像在 z 方向检查异质生物样本,以定性和半定量的方式构建 3D 模型。