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Flow-scanning optical tomography

Author(s): Pégard, Nicolas C; Toth, Marton L; Driscoll, Monica; Fleischer, Jason W

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dc.contributor.authorPégard, Nicolas C-
dc.contributor.authorToth, Marton L-
dc.contributor.authorDriscoll, Monica-
dc.contributor.authorFleischer, Jason W-
dc.date.accessioned2024-02-18T04:03:35Z-
dc.date.available2024-02-18T04:03:35Z-
dc.date.issued2014-08-07en_US
dc.identifier.citationPégard, Nicolas C, Toth, Marton L, Driscoll, Monica, Fleischer, Jason W. (Flow-scanning optical tomography. Lab Chip, 14 (23), 4447 - 4450. doi:10.1039/c4lc00701hen_US
dc.identifier.issn1473-0197-
dc.identifier.urihttp://arks.princeton.edu/ark:/88435/pr15t3g05n-
dc.description.abstractWe present a 3D tomography technique for in vivo observation of microscopic samples. The method combines flow in a microfluidic channel, illumination through a slit aperture, and a Fourier lens for simultaneous acquisition of multiple perspective angles in the phase-space domain. The technique is non-invasive and naturally robust to parasitic sample motion. 3D absorption is retrieved using standard back-projection algorithms, here a limited-domain inverse radon transform. Simultaneously, 3D differential phase contrast images are obtained by computational refocusing and comparison of complementary illumination angles. We implement the technique on a modified glass slide which can be mounted directly on existing optical microscopes. We demonstrate both amplitude and phase tomography on live, freely swimming C. elegans nematodes.en_US
dc.format.extent4447 - 4450en_US
dc.languageenen_US
dc.language.isoen_USen_US
dc.relation.ispartofLab on a Chipen_US
dc.rightsAuthor's manuscripten_US
dc.titleFlow-scanning optical tomographyen_US
dc.typeJournal Articleen_US
dc.identifier.doidoi:10.1039/c4lc00701h-
dc.identifier.eissn1473-0189-
pu.type.symplectichttp://www.symplectic.co.uk/publications/atom-terms/1.0/journal-articleen_US

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