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   <dc:title>Multiplane Encoded Light-Sheet Microscopy for Enhanced 3D Imaging</dc:title>
   <dc:creator>Zunino, Alessandro</dc:creator>
   <dc:creator>Garzella, Francesco</dc:creator>
   <dc:creator>Trianni, Alberta</dc:creator>
   <dc:creator>Saggau, Peter</dc:creator>
   <dc:creator>Bianchini, Paolo</dc:creator>
   <dc:creator>Diaspro, Alberto</dc:creator>
   <dc:creator>Duocastella, Martí</dc:creator>
   <dc:subject>Microscopis</dc:subject>
   <dc:subject>Visualització tridimensional</dc:subject>
   <dc:subject>Microscopes</dc:subject>
   <dc:subject>Three-dimensional display systems</dc:subject>
   <dcterms:abstract>Light-sheet microscopes have become the tool of choice for volumetric imaging of large samples. Based on a wide-field acquisition scheme, they are capable of optical sectioning at diffraction-limited resolution and minimal overall photodamage. Unfortunately, traditional architectures are limited in speed because 3D images are collected by either sample translation or synchronized movement of both light-sheet and detection objective lens. A promising solution avoiding slow mechanical movements is to extend the depth-of-field of the microscope and moving only the light-sheet. However, this normally comes at the cost of losing light and contrast, compromising the signal-to-noise ratio of the images. Here, we propose an innovative technique devoted to restoring the quality of the images, while preserving the speed of extended depth-of-field microscopes. It is based on generating a stack of parallel light-sheets using a pair of orthogonal acousto-optic deflectors, enabling the simultaneous illumination of different sample planes. Given the extended depth-of-field, all such planes appear in focus and can be acquired in a superimposed single frame. By applying a single-step inversion algorithm, we can decode a stack of frames into a volumetric image whose signal-to-noise ratio and contrast are greatly enhanced. We provide a detailed theoretical framework of the method and demonstrate its feasibility with volumetric images of kidney cell spheroids.</dcterms:abstract>
   <dcterms:issued>2022-02-18T09:24:14Z</dcterms:issued>
   <dcterms:issued>2022-02-18T09:24:14Z</dcterms:issued>
   <dcterms:issued>2021-11-03</dcterms:issued>
   <dcterms:issued>2022-02-18T09:24:14Z</dcterms:issued>
   <dc:type>info:eu-repo/semantics/article</dc:type>
   <dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
   <dc:relation>Reproducció del document publicat a: https://doi.org/10.1021/acsphotonics.1c01401</dc:relation>
   <dc:relation>ACS Photonics, 2021</dc:relation>
   <dc:relation>https://doi.org/10.1021/acsphotonics.1c01401</dc:relation>
   <dc:rights>(c) Zunino, Alessandro, et al., 2021</dc:rights>
   <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
   <dc:publisher>American Chemical Society</dc:publisher>
   <dc:source>Articles publicats en revistes (Física Aplicada)</dc:source>
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