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用于无透镜数字全息显微镜的低强度照明,使样品相互作用最小化。

Low-intensity illumination for lensless digital holographic microscopy with minimized sample interaction.

作者信息

Mirecki Bartosz, Rogalski Mikołaj, Arcab Piotr, Rogujski Piotr, Stanaszek Luiza, Józwik Michał, Trusiak Maciej

机构信息

Warsaw University of Technology, Institute of Micromechanics and Photonics, 8 Sw. A. Boboli St., 02-525 Warsaw, Poland.

Authors contributed equally to this work.

出版信息

Biomed Opt Express. 2022 Oct 10;13(11):5667-5682. doi: 10.1364/BOE.464367. eCollection 2022 Nov 1.

Abstract

Exposure to laser light alters cell culture examination via optical microscopic imaging techniques based on label-free coherent digital holography. To mitigate this detrimental feature, researchers tend to use a broader spectrum and lower intensity of illumination, which can decrease the quality of holographic imaging due to lower resolution and higher noise. We study the lensless digital holographic microscopy (LDHM) ability to operate in the low photon budget (LPB) regime to enable imaging of unimpaired live cells with minimized sample interaction. Low-cost off-the-shelf components are used, promoting the usability of such a straightforward approach. We show that recording data in the LPB regime (down to 7 µW of illumination power) does not limit the contrast or resolution of the hologram phase and amplitude reconstruction compared to regular illumination. The LPB generates hardware camera shot noise, however, to be effectively minimized via numerical denoising. The ability to obtain high-quality, high-resolution optical complex field reconstruction was confirmed using the USAF 1951 amplitude sample, phase resolution test target, and finally, live glial restricted progenitor cells (as a challenging strongly absorbing and scattering biomedical sample). The proposed approach based on severely limiting the photon budget in lensless holographic microscopy method can open new avenues in high-throughout (optimal resolution, large field-of-view, and high signal-to-noise-ratio single-hologram reconstruction) cell culture imaging with minimized sample interaction.

摘要

通过基于无标记相干数字全息术的光学显微成像技术,激光照射会改变细胞培养检查。为减轻这一有害特性,研究人员倾向于使用更宽的光谱和更低的照明强度,然而这会因分辨率降低和噪声增加而降低全息成像的质量。我们研究了无透镜数字全息显微镜(LDHM)在低光子预算(LPB)模式下的运行能力,以实现对未受损活细胞的成像,并使样品相互作用最小化。使用了低成本的现成组件,提高了这种简单方法的可用性。我们表明,与常规照明相比,在LPB模式下记录数据(照明功率低至7微瓦)不会限制全息图相位和幅度重建的对比度或分辨率。然而,LPB会产生硬件相机散粒噪声,需要通过数值去噪有效地将其最小化。使用美国空军1951幅度样本、相位分辨率测试靶标,最后使用活的神经胶质限制性祖细胞(作为具有挑战性的强吸收和散射生物医学样本),证实了获得高质量、高分辨率光学复场重建的能力。基于在无透镜全息显微镜方法中严格限制光子预算的所提出方法,可以在高吞吐量(最佳分辨率、大视场和高信噪比单全息图重建)细胞培养成像中开辟新途径,同时使样品相互作用最小化。

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