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Immersion Mirau interferometry for label-free live cell imaging in an epi-illumination geometry

机译:沉浸式Mirau干涉术用于落射照明几何中的无标签活细胞成像

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In cell biology studies it is often important to avoid the damaging effects caused by fluorescent stains or UV-light. Immersion Mirau Interferometry (IMI) is an epi-illumination label-free imaging technique developed at the Columbia University Radiological Research Accelerator Facility. It is based on the principles of phase-shifting interferometry (PSI) and represents a novel approach for interferometric imaging of living cells in medium. To accommodate the use of medium, a custom immersion Mirau interferometric attachment was designed and built in-house. The space between the reference mirror and the beam splitter is filled with liquid to ensure identical optical paths in the test and reference arms. The interferometer is mountable onto a microscope objective. The greatest limitation of standard PSI is the sensitivity to environmental vibrations, because it requires consecutive acquisition of several interferograms. We are developing Simultaneous Immersion Mirau Interferometry (SIMI), which facilitates simultaneous acquisition of all interferograms and eliminates the effects of vibration. Polarization optics, incorporated into the design, introduces a phase delay to one of the components of the test beam. This enables simultaneous creation and spatial separation of two interferograms, which are combined with the background image to reconstruct the intensity map of the specimen. Our results of imaging live and fixed cells with IMI and SIMI show that this system produces images of a quality that is sufficient to perform targeted cellular irradiation experiments.
机译:在细胞生物学研究中,避免荧光染料或紫外线引起的破坏作用通常很重要。浸入式Mirau干涉测量(IMI)是由哥伦比亚大学放射研究加速器设施开发的无Epi照明标签的成像技术。它基于相移干涉术(PSI)的原理,代表了一种对培养基中活细胞进行干涉成像的新颖方法。为了适应介质的使用,在内部设计并制造了定制的Mirau浸入式干涉仪附件。参考镜和分束器之间的空间充满液体,以确保测试臂和参考臂中的光路相同。干涉仪可安装在显微镜物镜上。标准PSI的最大局限性是对环境振动的敏感性,因为它需要连续采集几个干涉图。我们正在开发同时浸没Mirau干涉术(SIMI),该技术有助于同时采集所有干涉图并消除振动的影响。纳入设计的偏振光学器件将相位延迟引入到测试光束的组件之一。这样可以同时创建和空间分离两个干涉图,将其与背景图像结合以重建样本的强度图。我们用IMI和SIMI对活细胞和固定细胞成像的结果表明,该系统产生的图像质量足以执行靶向细胞辐照实验。

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