| Literature DB >> 24049686 |
Diwakar Turaga1, Timothy E Holy.
Abstract
Light sheet microscopy allows rapid imaging of three-dimensional fluorescent samples, using illumination and detection axes that are orthogonal. For imaging large samples, this often forces the objective to be tilted relative to the sample's surface; for samples that are not precisely matched to the immersion medium index, this tilt introduces aberrations. Here we calculate the nature of these aberrations for a simple tissue model, and show that a low-dimensional parametrization of these aberrations facilitates online correction via a deformable mirror without introduction of beads or other fiducial markers. We use this approach to demonstrate improved image quality in living tissue.Keywords: (110.1080) Active or adaptive optics; (180.2520) Fluorescence microscopy
Year: 2013 PMID: 24049686 PMCID: PMC3771836 DOI: 10.1364/BOE.4.001654
Source DB: PubMed Journal: Biomed Opt Express ISSN: 2156-7085 Impact factor: 3.732