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Quantitative imaging of yeast cells using transport of intensity equation

机译:使用强度方程传输对酵母细胞进行定量成像

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In biology most microscopy specimens, in particular living cells are transparent. In cell imaging, it is hard to create an image of a cell which is transparent with a very small refractive index change with respect to the surrounding media. Various techniques like addition of staining and contrast agents, markers have been applied in the past for creating contrast. Many of the staining agents or markers are not applicable to live cell imaging as they are toxic. In this paper, we report theoretical and experimental results from quantitative phase imaging of yeast cells with a commercial bright field microscope. We reconstruct the phase of cells non-interferometrically based on the transport of intensity equations (TIE). This technique estimates the axial derivative from positive through-focus intensity measurements. This technique allows phase imaging using a regular microscope with white light illumination. We demonstrate nano-metric depth sensitivity in imaging live yeast cells using this technique. Experimental results will be shown in the paper demonstrating the capability of the technique in 3-D volume estimation of living cells. This real-time imaging technique would be highly promising in real-time digital pathology applications, screening of pathogens and staging of diseases like malaria as it does not need any preprocessing of samples.
机译:在生物学上,大多数显微镜标本,特别是活细胞都是透明的。在细胞成像中,难以产生透明的细胞图像,该图像相对于周围介质具有非常小的折射率变化。过去已经采用了各种技术,例如添加染色剂和对比剂,标记物来产生对比。许多染色剂或标记物有毒,因此不适用于活细胞成像。在本文中,我们报告了使用商业明场显微镜对酵母细胞进行定量相成像的理论和实验结果。我们基于强度方程式(TIE)的传输以非干涉方式重建细胞的相位。该技术从正焦强度测量值估算轴向导数。该技术允许使用带有白光照明的常规显微镜进行相位成像。我们展示了使用这种技术对活酵母细胞成像的纳米深度敏感性。实验结果将在论文中显示,证明该技术在活细胞3-D体积估计中的能力。这种实时成像技术在实时数字病理学应用,病原体筛查和疟疾等疾病的分期中非常有前途,因为它不需要任何样品预处理。

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