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使用单束相位恢复方法进行定量细胞成像。

Quantitative cell imaging using single beam phase retrieval method.

出版信息

J Biomed Opt. 2011 Jun;16(6):060503. doi: 10.1117/1.3589090.

Abstract

Quantitative three-dimensional imaging of cells can provide important information about their morphology as well as their dynamics, which will be useful in studying their behavior under various conditions. There are several microscopic techniques to image unstained, semi-transparent specimens, by converting the phase information into intensity information. But most of the quantitative phase contrast imaging techniques is realized either by using interference of the object wavefront with a known reference beam or using phase shifting interferometry. A two-beam interferometric method is challenging to implement especially with low coherent sources and it also requires a fine adjustment of beams to achieve high contrast fringes. In this letter, the development of a single beam phase retrieval microscopy technique for quantitative phase contrast imaging of cells using multiple intensity samplings of a volume speckle field in the axial direction is described. Single beam illumination with multiple intensity samplings provides fast convergence and a unique solution of the object wavefront. Three-dimensional thickness profiles of different cells such as red blood cells and onion skin cells were reconstructed using this technique with an axial resolution of the order of several nanometers.

摘要

细胞的定量三维成像是获取细胞形态及其动力学信息的重要手段,这些信息对于研究细胞在不同条件下的行为非常有用。有几种显微镜技术可以对未经染色的半透明标本进行成像,通过将相位信息转换为强度信息来实现。但大多数定量相位对比成像技术要么是通过物体波前与已知参考光束的干涉来实现,要么是通过相移干涉测量来实现。双光束干涉方法实施起来具有挑战性,特别是对于低相干光源而言,并且还需要对光束进行精细调整以实现高对比度条纹。在这封信件中,描述了一种使用体积散斑场在轴向方向上进行多次强度采样的单光束相位恢复显微镜技术,用于对细胞进行定量相位对比成像。单光束照明与多次强度采样相结合,可以快速收敛并获得物体波前的唯一解。使用该技术可以重建不同细胞(如红细胞和洋葱皮细胞)的三维厚度轮廓,轴向分辨率可达数纳米。

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