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      Wide-field computational imaging of pathology slides using lens-free on-chip microscopy.

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          Abstract

          Optical examination of microscale features in pathology slides is one of the gold standards to diagnose disease. However, the use of conventional light microscopes is partially limited owing to their relatively high cost, bulkiness of lens-based optics, small field of view (FOV), and requirements for lateral scanning and three-dimensional (3D) focus adjustment. We illustrate the performance of a computational lens-free, holographic on-chip microscope that uses the transport-of-intensity equation, multi-height iterative phase retrieval, and rotational field transformations to perform wide-FOV imaging of pathology samples with comparable image quality to a traditional transmission lens-based microscope. The holographically reconstructed image can be digitally focused at any depth within the object FOV (after image capture) without the need for mechanical focus adjustment and is also digitally corrected for artifacts arising from uncontrolled tilting and height variations between the sample and sensor planes. Using this lens-free on-chip microscope, we successfully imaged invasive carcinoma cells within human breast sections, Papanicolaou smears revealing a high-grade squamous intraepithelial lesion, and sickle cell anemia blood smears over a FOV of 20.5 mm(2). The resulting wide-field lens-free images had sufficient image resolution and contrast for clinical evaluation, as demonstrated by a pathologist's blinded diagnosis of breast cancer tissue samples, achieving an overall accuracy of ~99%. By providing high-resolution images of large-area pathology samples with 3D digital focus adjustment, lens-free on-chip microscopy can be useful in resource-limited and point-of-care settings.

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          Most cited references37

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          Stable signal recovery from incomplete and inaccurate measurements

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            Deterministic phase retrieval: a Green’s function solution

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              Imaging without lenses: achievements and remaining challenges of wide-field on-chip microscopy.

              We discuss unique features of lens-free computational imaging tools and report some of their emerging results for wide-field on-chip microscopy, such as the achievement of a numerical aperture (NA) of ∼0.8-0.9 across a field of view (FOV) of more than 20 mm(2) or an NA of ∼0.1 across a FOV of ∼18 cm(2), which corresponds to an image with more than 1.5 gigapixels. We also discuss the current challenges that these computational on-chip microscopes face, shedding light on their future directions and applications.
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                Author and article information

                Journal
                Sci Transl Med
                Science translational medicine
                1946-6242
                1946-6234
                Dec 17 2014
                : 6
                : 267
                Affiliations
                [1 ] Electrical Engineering Department, University of California, Los Angeles, Los Angeles, CA 90095, USA. Department of Bioengineering, University of California, Los Angeles, Los Angeles, CA 90095, USA. California NanoSystems Institute, University of California, Los Angeles, Los Angeles, CA 90095, USA.
                [2 ] Department of Bioengineering, University of California, Los Angeles, Los Angeles, CA 90095, USA.
                [3 ] Electrical Engineering Department, University of California, Los Angeles, Los Angeles, CA 90095, USA.
                [4 ] Department of Pathology and Laboratory Medicine, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA 90095, USA.
                [5 ] Electrical Engineering Department, University of California, Los Angeles, Los Angeles, CA 90095, USA. Department of Bioengineering, University of California, Los Angeles, Los Angeles, CA 90095, USA. California NanoSystems Institute, University of California, Los Angeles, Los Angeles, CA 90095, USA. Department of Surgery, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA 90095, USA. ozcan@ucla.edu.
                Article
                6/267/267ra175
                10.1126/scitranslmed.3009850
                25520396
                ab2d7d6a-c82b-4607-bbf1-3051d4fd9369
                Copyright © 2014, American Association for the Advancement of Science.
                History

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