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dc.contributor.authorLiang, Kaicheng
dc.contributor.authorWang, Zhao
dc.contributor.authorAhsen, Osman Oguz
dc.contributor.authorLee, Hsiang-Chieh
dc.contributor.authorPotsaid, Benjamin M.
dc.contributor.authorJayaraman, Vijaysekhar
dc.contributor.authorCable, Alex
dc.contributor.authorMashimo, Hiroshi
dc.contributor.authorLi, Xingde
dc.contributor.authorFujimoto, James G
dc.date.accessioned2019-06-27T18:04:21Z
dc.date.available2019-06-27T18:04:21Z
dc.date.issued2018-01
dc.date.submitted2017-11
dc.identifier.issn2334-2536
dc.identifier.urihttps://hdl.handle.net/1721.1/121433
dc.description.abstractDevices that perform wide field-of-view (FOV) precision optical scanning are important for endoscopic assessment and diagnosis of luminal organ disease such as in gastroenterology. Optical scanning for in vivo endoscopic imaging has traditionally relied on one or more proximal mechanical actuators, limiting scan accuracy and imaging speed. There is a need for rapid and precise two-dimensional (2D) microscanning technologies to enable the translation of benchtop scanning microscopies to in vivo endoscopic imaging. We demonstrate a new cycloid scanner in a tethered capsule for ultrahigh speed, side-viewing optical coherence tomography (OCT) endomicroscopy in vivo. The cycloid capsule incorporates two scanners: a piezoelectrically actuated resonant fiber scanner to perform a precision, small FOV, fast scan and a micromotor scanner to perform a wide FOV, slow scan. Together these scanners distally scan the beam circumferentially in a 2D cycloid pattern, generating an unwrapped1 mm× 38 mm strip FOV. Sequential strip volumes can be acquired with proximal pullback to image centimeter-long regions. Using ultrahigh speed 1.3 μm wavelength swept-source OCT at a 1.17 MHz axial scan rate, we imaged the human rectum at 3 volumes/s. Each OCT strip volume had 166 × 2322 axial scans with 8.5 μm axial and 30 μm transverse resolution. We further demonstrate OCT angiography at 0.5 volumes/s, producing volumetric images of vasculature. In addition to OCT applications, cycloid scanning promises to enable precision 2D optical scanning for other imaging modalities, including fluorescence confocal and nonlinear microscopy.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant R01-CA075289)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant R01-CA178636)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant R01-EY011289)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant R44-CA101067)en_US
dc.description.sponsorshipAir Force Office of Scientific Research (Grant FA9550-12-1- 0499)en_US
dc.description.sponsorshipAir Force Office of Scientific Research (Grant FA9550-15-1-0473)en_US
dc.language.isoen
dc.publisherOSA Publishingen_US
dc.relation.isversionofhttp://dx.doi.org/10.1364/OPTICA.5.000036en_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alikeen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/en_US
dc.sourcePMCen_US
dc.titleCycloid scanning for wide field optical coherence tomography endomicroscopy and angiography in vivoen_US
dc.typeArticleen_US
dc.identifier.citationLiang, Kaicheng et al. "Cycloid scanning for wide field optical coherence tomography endomicroscopy and angiography in vivo." Optica 5, 1 (January 2018): 36-43 © 2018 Optical Society of Americaen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Electrical Engineering and Computer Scienceen_US
dc.contributor.departmentMassachusetts Institute of Technology. Research Laboratory of Electronicsen_US
dc.relation.journalOpticaen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2019-06-26T16:06:27Z
dspace.date.submission2019-06-26T16:06:28Z
mit.journal.volume5en_US
mit.journal.issue1en_US


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