| Literature DB >> 30258669 |
Sebastian Bohn1, Karsten Sperlich1, Stephan Allgeier2, Andreas Bartschat2, Ruby Prakasam1, Klaus-Martin Reichert2, Heinrich Stolz3, Rudolf Guthoff1, Ralf Mikut2, Bernd Köhler2, Oliver Stachs1.
Abstract
We present an in vivo confocal laser scanning microscopy based method for large 3D reconstruction of the cornea on a cellular level with cropped volume sizes up to 266 x 286 x 396 µm3. The microscope objective used is equipped with a piezo actuator for automated, fast and precise closed-loop focal plane control. Furthermore, we present a novel concave surface contact cap, which significantly reduces eye movements by up to 87%, hence increasing the overlapping image area of the whole stack. This increases the cuboid volume of the generated 3D reconstruction significantly. The possibility to generate oblique sections using isotropic volume stacks opens the window to slit lamp microscopy on a cellular level.Keywords: (170.1790) Confocal microscopy; (170.3880) Medical and biological imaging; (170.4470) Ophthalmology
Year: 2018 PMID: 30258669 PMCID: PMC6154195 DOI: 10.1364/BOE.9.002511
Source DB: PubMed Journal: Biomed Opt Express ISSN: 2156-7085 Impact factor: 3.732