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Conference Paper: Ultralarge-scale spinning time-stretch quantitative phase imaging system for label-free cell and tissue imaging
Title | Ultralarge-scale spinning time-stretch quantitative phase imaging system for label-free cell and tissue imaging |
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Authors | |
Issue Date | 2019 |
Publisher | SPIE - International Society for Optical Engineering. The Journal's web site is located at http://spie.org/x1848.xml?WT.svl=mddp2 |
Citation | Proceedings of SPIE Photonics West BIOS 2019, San Francisco, California, USA, 2-7 February 2019, v. 10889, article no. 108890U How to Cite? |
Abstract | Continuing development of image-based bioassay is mainly hampered by the lack of throughput to systematically screen a large cell/tissue population under extensive experimental conditions; and the overwhelming reliance on biochemical markers, which are not always effective, especially when there is poor prior knowledge of the markers. Here we demonstrate ultralarge-scale, high-resolution “on-the-fly” quantitative phase imaging (QPI) of single-cells and whole-tissue-slide on a spinning-disk assay platform at an imaging rate of at least 100-times faster than current assays – mitigating the imaging throughput limitation hindered by the fundamental space-bandwidth-product limit of classical optical imaging. The concept takes advantage of the high-speed spinning motion, which naturally provides imaging at an ultrafast rate (<10MHz) that can only be made possible with time-stretch imaging. To demonstrate the capability of the system, we imaged both label-free adherent cells and tissue slices, prepared on the functionalized digital versatile discs (DVDs), across a giga-pixel-FOV exceeding 10mm2 at a resolution of ~ 1μm. Both bright-field and QPI images are generated in real-time with this FOV at a spinning speed of <1,000 rpm. In contrast to the vast majority of current QPI modalities, our platform requires no interferometry and no computationally-intensive iterative method for phase retrieval, favouring continuous high-speed QPI operation in real-time. More importantly, this spinning imaging platform allows generation of a catalogue of label-free biophysical phenotypes of cells/tissues, e.g. cell size, dry mass density, morphology as well as light scattering properties, which could enable a new generation of large-scale in-depth label-free image-based bioassays. |
Description | v. 10889 title: High-Speed Biomedical Imaging and Spectroscopy IV |
Persistent Identifier | http://hdl.handle.net/10722/275261 |
DC Field | Value | Language |
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dc.contributor.author | Siu, MDD | - |
dc.contributor.author | Tang, AHL | - |
dc.contributor.author | Lee, KCM | - |
dc.contributor.author | Wong, KKY | - |
dc.contributor.author | Tsia, KKM | - |
dc.date.accessioned | 2019-09-10T02:38:56Z | - |
dc.date.available | 2019-09-10T02:38:56Z | - |
dc.date.issued | 2019 | - |
dc.identifier.citation | Proceedings of SPIE Photonics West BIOS 2019, San Francisco, California, USA, 2-7 February 2019, v. 10889, article no. 108890U | - |
dc.identifier.uri | http://hdl.handle.net/10722/275261 | - |
dc.description | v. 10889 title: High-Speed Biomedical Imaging and Spectroscopy IV | - |
dc.description.abstract | Continuing development of image-based bioassay is mainly hampered by the lack of throughput to systematically screen a large cell/tissue population under extensive experimental conditions; and the overwhelming reliance on biochemical markers, which are not always effective, especially when there is poor prior knowledge of the markers. Here we demonstrate ultralarge-scale, high-resolution “on-the-fly” quantitative phase imaging (QPI) of single-cells and whole-tissue-slide on a spinning-disk assay platform at an imaging rate of at least 100-times faster than current assays – mitigating the imaging throughput limitation hindered by the fundamental space-bandwidth-product limit of classical optical imaging. The concept takes advantage of the high-speed spinning motion, which naturally provides imaging at an ultrafast rate (<10MHz) that can only be made possible with time-stretch imaging. To demonstrate the capability of the system, we imaged both label-free adherent cells and tissue slices, prepared on the functionalized digital versatile discs (DVDs), across a giga-pixel-FOV exceeding 10mm2 at a resolution of ~ 1μm. Both bright-field and QPI images are generated in real-time with this FOV at a spinning speed of <1,000 rpm. In contrast to the vast majority of current QPI modalities, our platform requires no interferometry and no computationally-intensive iterative method for phase retrieval, favouring continuous high-speed QPI operation in real-time. More importantly, this spinning imaging platform allows generation of a catalogue of label-free biophysical phenotypes of cells/tissues, e.g. cell size, dry mass density, morphology as well as light scattering properties, which could enable a new generation of large-scale in-depth label-free image-based bioassays. | - |
dc.language | eng | - |
dc.publisher | SPIE - International Society for Optical Engineering. The Journal's web site is located at http://spie.org/x1848.xml?WT.svl=mddp2 | - |
dc.relation.ispartof | SPIE Photonics West BIOS 2019 | - |
dc.rights | SPIE - International Society for Optical Engineering. Proceedings. Copyright © SPIE - International Society for Optical Engineering. | - |
dc.title | Ultralarge-scale spinning time-stretch quantitative phase imaging system for label-free cell and tissue imaging | - |
dc.type | Conference_Paper | - |
dc.identifier.email | Wong, KKY: kywong@eee.hku.hk | - |
dc.identifier.email | Tsia, KKM: tsia@hku.hk | - |
dc.identifier.authority | Wong, KKY=rp00189 | - |
dc.identifier.authority | Tsia, KKM=rp01389 | - |
dc.identifier.doi | 10.1117/12.2508354 | - |
dc.identifier.hkuros | 303733 | - |
dc.identifier.volume | 10889 | - |
dc.identifier.spage | 108890U | - |
dc.identifier.epage | 108890U | - |
dc.publisher.place | United States | - |