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LIPID PARTICLE DETECTION BY MEANS DIGITAL HOLOGRAPHY AND LATERAL SHEAR INTERFEROMETRY

机译:通过数字全息和横向剪切干涉法检测脂质颗粒

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Digital Holography in microscope configuration thanks to the numerical reconstruction procedure is a flexible and useful tool for analysis of biological material. We present the investigation of lipid particles growth in in-vitro mouse cell using a Digital Holographic Microscopy (DHM) employed in combination with Lateral Shear Interferometry (LSI). The optical setup is based on a Mach-Zehnder interferometer in transmission geometry. The sample cell is placed in one interferometer arm while the other one is used as a reference beam. By means of the Rayleigh-Sommerfield integral is possible to retrieve the complex object field and then to calculate the amplitude and phase of the laser light transmitted by the sample. Traditional microscopy allows to obtain amplitude contrast image only, DH, instead, enables to calculate the phase map of the complex wave that is simply related to the optical phase difference (OPD) experienced by the light when it is transmitted through the object. In this way it is possible to obtain phase contrast image that is very useful for biological materials that often present low amplitude contrast for quantitative amplitude image. The main difficulty of this technique is to remove the optical aberrations produced by the optical setup components. Several methods have been proposed, such as subtraction of a reference phase map (without sample) or numerical multiplication of a parametric lens. We propose a fast and effective solution of this problem based on LSI. We digitally introduce a lateral shear of one pixel in x and y directions calculating the phase difference △Φ_(x,y), between the actual phase map and its sheared replica in both directions. △Φ_(x,y) include a linear term due to defocus aberration and the object phase difference. The linear term can be easily eliminated and sample phase map retrieved by numerical integration. This technique allows to obtain the correct phase contrast image removing optical aberration, avoiding unwrapping problems.
机译:借助数字重建程序,显微镜配置中的数字全息照相术是一种用于分析生物材料的灵活而有用的工具。我们目前使用与横向剪切干涉术(LSI)结合使用的数字全息显微镜(DHM)对体外小鼠细胞中脂质颗粒生长的研究。光学设置基于传输几何学中的Mach-Zehnder干涉仪。样品池放置在一个干涉仪臂中,而另一个则用作参考光束。借助于瑞利-索姆菲尔德积分,有可能取回复杂的物场,然后计算样品透射的激光的振幅和相位。传统的显微镜只能获取振幅对比图像,而DH却可以计算复杂波的相位图,该相位图与光在通过对象时所经历的光学相位差(OPD)简单相关。以这种方式,可以获得对于生物材料非常有用的相位衬度图像,该生物材料对于定量振幅图像常常呈现低振幅衬度。该技术的主要困难是消除由光学设置组件产生的光学像差。已经提出了几种方法,例如减去参考相位图(无样本)或参数化透镜的数值乘法。我们提出了一种基于LSI的快速有效的解决方案。我们以数字方式在x和y方向上引入一个像素的横向剪切,以计算实际相位图及其在两个方向上的剪切副本之间的相位差△Φ_(x,y)。由于散焦像差和物体相位差,△Φ_(x,y)包括一个线性项。线性项可以很容易地消除,并且可以通过数值积分来检索样本相位图。该技术允许获得消除光学像差的正确相衬图像,从而避免出现开卷问题。

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