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      Method for single illumination source combined optical coherence tomography and fluorescence imaging of fluorescently labeled ocular structures in transgenic mice

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          Abstract

          In vivo imaging permits longitudinal study of ocular disease processes in the same animal over time. Two different in vivo optical imaging modalities – optical coherence tomography (OCT) and fluorescence – provide important structural and cellular data respectively about disease processes. In this Methods in Eye Research article, we describe and demonstrate the combination of these two modalities producing a truly simultaneous OCT and fluorescence imaging system for imaging of fluorescently labeled animal models. This system uses only a single light source to illuminate both modalities, and both share the same field of view. This allows simultaneous acquisition of OCT and fluorescence images, and the benefits of both techniques are realized without incurring increased costs in variability, light exposure, time, and post-processing effort as would occur when the modalities are used separately. We then utilized this system to demonstrate multi-modal imaging in a progression of samples exhibiting both fluorescence and OCT scattering beginning with resolution targets, ex vivo thy1-YFP labeled neurons in mouse eyes, and finally an in vivo longitudinal time course of GFP labelled myeloid cells in a mouse model of ocular allergy.

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          Author and article information

          Journal
          0370707
          3647
          Exp Eye Res
          Exp. Eye Res.
          Experimental eye research
          0014-4835
          1096-0007
          15 October 2016
          09 August 2016
          October 2016
          01 October 2017
          : 151
          : 68-74
          Affiliations
          [1 ]Duke Eye Center and Department of Ophthalmology, Duke University Medical Center, Durham, NC 27710
          [2 ]Department of Biomedical Engineering, Duke University, Durham, NC 27708
          Author notes
          [* ] Corresponding Author: Ryan P. McNabb, ryan.mcnabb@ 123456dm.duke.edu
          Article
          PMC5072542 PMC5072542 5072542 nihpa823314
          10.1016/j.exer.2016.08.003
          5072542
          27519152
          82a11778-aaf7-4860-afd3-1f784bbe0cef
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