| Literature DB >> 34274370 |
Pietro Ricci1, Vladislav Gavryusev1, Caroline Müllenbroich2, Lapo Turrini1, Giuseppe de Vito3, Ludovico Silvestri4, Giuseppe Sancataldo5, Francesco Saverio Pavone6.
Abstract
In recent years, light-sheet fluorescence microscopy (LSFM) has found a broad application for imaging of diverse biological samples, ranging from sub-cellular structures to whole animals, both in-vivo and ex-vivo, owing to its many advantages relative to point-scanning methods. By providing the selective illumination of sample single planes, LSFM achieves an intrinsic optical sectioning and direct 2D image acquisition, with low out-of-focus fluorescence background, sample photo-damage and photo-bleaching. On the other hand, such an illumination scheme is prone to light absorption or scattering effects, which lead to uneven illumination and striping artifacts in the images, oriented along the light sheet propagation direction. Several methods have been developed to address this issue, ranging from fully optical solutions to entirely digital post-processing approaches. In this work, we present them, outlining their advantages, performance and limitations.Entities:
Keywords: 3D microscopy; Brain imaging; Light-sheet microscopy; Striping
Mesh:
Year: 2021 PMID: 34274370 DOI: 10.1016/j.pbiomolbio.2021.07.003
Source DB: PubMed Journal: Prog Biophys Mol Biol ISSN: 0079-6107 Impact factor: 3.667