Wide Field-of-View Microscopes and Endoscopes for Time-Lapse Imaging and High-Throughput Screening

<p>Wide field-of-view (FOV) microscopy is of high importance to biological research and clinical diagnosis where a high-throughput screening of samples is needed. This thesis presents the development of several novel wide FOV imaging technologies and demonstrates their capabilities in longitud...

Full description

Bibliographic Details
Main Author: Han, Chao
Format: Others
Published: 2015
Online Access:https://thesis.library.caltech.edu/8763/1/Han_Chao_2015_Thesis.pdf
Han, Chao (2015) Wide Field-of-View Microscopes and Endoscopes for Time-Lapse Imaging and High-Throughput Screening. Dissertation (Ph.D.), California Institute of Technology. doi:10.7907/Z9SF2T49. https://resolver.caltech.edu/CaltechTHESIS:01302015-101318815 <https://resolver.caltech.edu/CaltechTHESIS:01302015-101318815>
id ndltd-CALTECH-oai-thesis.library.caltech.edu-8763
record_format oai_dc
spelling ndltd-CALTECH-oai-thesis.library.caltech.edu-87632019-10-05T03:03:23Z Wide Field-of-View Microscopes and Endoscopes for Time-Lapse Imaging and High-Throughput Screening Han, Chao <p>Wide field-of-view (FOV) microscopy is of high importance to biological research and clinical diagnosis where a high-throughput screening of samples is needed. This thesis presents the development of several novel wide FOV imaging technologies and demonstrates their capabilities in longitudinal imaging of living organisms, on the scale of viral plaques to live cells and tissues.</p> <p>The ePetri Dish is a wide FOV on-chip bright-field microscope. Here we applied an ePetri platform for plaque analysis of murine norovirus 1 (MNV-1). The ePetri offers the ability to dynamically track plaques at the individual cell death event level over a wide FOV of 6 mm × 4 mm at 30 min intervals. A density-based clustering algorithm is used to analyze the spatial-temporal distribution of cell death events to identify plaques at their earliest stages. We also demonstrate the capabilities of the ePetri in viral titer count and dynamically monitoring plaque formation, growth, and the influence of antiviral drugs.</p> <p>We developed another wide FOV imaging technique, the Talbot microscope, for the fluorescence imaging of live cells. The Talbot microscope takes advantage of the Talbot effect and can generate a focal spot array to scan the fluorescence samples directly on-chip. It has a resolution of 1.2 μm and a FOV of ~13 mm<sup>2</sup>. We further upgraded the Talbot microscope for the long-term time-lapse fluorescence imaging of live cell cultures, and analyzed the cells’ dynamic response to an anticancer drug.</p> <p>We present two wide FOV endoscopes for tissue imaging, named the AnCam and the PanCam. The AnCam is based on the contact image sensor (CIS) technology, and can scan the whole anal canal within 10 seconds with a resolution of 89 μm, a maximum FOV of 100 mm × 120 mm, and a depth-of-field (DOF) of 0.65 mm. We also demonstrate the performance of the AnCam in whole anal canal imaging in both animal models and real patients. In addition to this, the PanCam is based on a smartphone platform integrated with a panoramic annular lens (PAL), and can capture a FOV of 18 mm × 120 mm in a single shot with a resolution of 100─140 μm. In this work we demonstrate the PanCam’s performance in imaging a stained tissue sample.</p> 2015 Thesis NonPeerReviewed application/pdf https://thesis.library.caltech.edu/8763/1/Han_Chao_2015_Thesis.pdf https://resolver.caltech.edu/CaltechTHESIS:01302015-101318815 Han, Chao (2015) Wide Field-of-View Microscopes and Endoscopes for Time-Lapse Imaging and High-Throughput Screening. Dissertation (Ph.D.), California Institute of Technology. doi:10.7907/Z9SF2T49. https://resolver.caltech.edu/CaltechTHESIS:01302015-101318815 <https://resolver.caltech.edu/CaltechTHESIS:01302015-101318815> https://thesis.library.caltech.edu/8763/
collection NDLTD
format Others
sources NDLTD
description <p>Wide field-of-view (FOV) microscopy is of high importance to biological research and clinical diagnosis where a high-throughput screening of samples is needed. This thesis presents the development of several novel wide FOV imaging technologies and demonstrates their capabilities in longitudinal imaging of living organisms, on the scale of viral plaques to live cells and tissues.</p> <p>The ePetri Dish is a wide FOV on-chip bright-field microscope. Here we applied an ePetri platform for plaque analysis of murine norovirus 1 (MNV-1). The ePetri offers the ability to dynamically track plaques at the individual cell death event level over a wide FOV of 6 mm × 4 mm at 30 min intervals. A density-based clustering algorithm is used to analyze the spatial-temporal distribution of cell death events to identify plaques at their earliest stages. We also demonstrate the capabilities of the ePetri in viral titer count and dynamically monitoring plaque formation, growth, and the influence of antiviral drugs.</p> <p>We developed another wide FOV imaging technique, the Talbot microscope, for the fluorescence imaging of live cells. The Talbot microscope takes advantage of the Talbot effect and can generate a focal spot array to scan the fluorescence samples directly on-chip. It has a resolution of 1.2 μm and a FOV of ~13 mm<sup>2</sup>. We further upgraded the Talbot microscope for the long-term time-lapse fluorescence imaging of live cell cultures, and analyzed the cells’ dynamic response to an anticancer drug.</p> <p>We present two wide FOV endoscopes for tissue imaging, named the AnCam and the PanCam. The AnCam is based on the contact image sensor (CIS) technology, and can scan the whole anal canal within 10 seconds with a resolution of 89 μm, a maximum FOV of 100 mm × 120 mm, and a depth-of-field (DOF) of 0.65 mm. We also demonstrate the performance of the AnCam in whole anal canal imaging in both animal models and real patients. In addition to this, the PanCam is based on a smartphone platform integrated with a panoramic annular lens (PAL), and can capture a FOV of 18 mm × 120 mm in a single shot with a resolution of 100─140 μm. In this work we demonstrate the PanCam’s performance in imaging a stained tissue sample.</p>
author Han, Chao
spellingShingle Han, Chao
Wide Field-of-View Microscopes and Endoscopes for Time-Lapse Imaging and High-Throughput Screening
author_facet Han, Chao
author_sort Han, Chao
title Wide Field-of-View Microscopes and Endoscopes for Time-Lapse Imaging and High-Throughput Screening
title_short Wide Field-of-View Microscopes and Endoscopes for Time-Lapse Imaging and High-Throughput Screening
title_full Wide Field-of-View Microscopes and Endoscopes for Time-Lapse Imaging and High-Throughput Screening
title_fullStr Wide Field-of-View Microscopes and Endoscopes for Time-Lapse Imaging and High-Throughput Screening
title_full_unstemmed Wide Field-of-View Microscopes and Endoscopes for Time-Lapse Imaging and High-Throughput Screening
title_sort wide field-of-view microscopes and endoscopes for time-lapse imaging and high-throughput screening
publishDate 2015
url https://thesis.library.caltech.edu/8763/1/Han_Chao_2015_Thesis.pdf
Han, Chao (2015) Wide Field-of-View Microscopes and Endoscopes for Time-Lapse Imaging and High-Throughput Screening. Dissertation (Ph.D.), California Institute of Technology. doi:10.7907/Z9SF2T49. https://resolver.caltech.edu/CaltechTHESIS:01302015-101318815 <https://resolver.caltech.edu/CaltechTHESIS:01302015-101318815>
work_keys_str_mv AT hanchao widefieldofviewmicroscopesandendoscopesfortimelapseimagingandhighthroughputscreening
_version_ 1719261018896465920