Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/32815
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dc.contributor.authorKoho, Sami, V-
dc.contributor.authorSLENDERS, Eli-
dc.contributor.authorTortarolo, Giorgio-
dc.contributor.authorCastello, Marco-
dc.contributor.authorButtafava, Mauro-
dc.contributor.authorVilla, Federica-
dc.contributor.authorTcarenkova, Elena-
dc.contributor.authorAMELOOT, Marcel-
dc.contributor.authorBianchini, Paolo-
dc.contributor.authorSheppard, Colin J. R.-
dc.contributor.authorDiaspro, Alberto-
dc.contributor.authorTosi, Alberto-
dc.contributor.authorVicidomini, Giuseppe-
dc.date.accessioned2020-12-09T09:35:31Z-
dc.date.available2020-12-09T09:35:31Z-
dc.date.issued2020-
dc.date.submitted2020-11-12T12:37:34Z-
dc.identifier.citationBIOMEDICAL OPTICS EXPRESS, 11(6), p. 2905-2924-
dc.identifier.urihttp://hdl.handle.net/1942/32815-
dc.description.abstractTwo-photon excitation (2PE) laser scanning microscopy is the imaging modality of choice when one desires to work with thick biological samples. However, its spatial resolution is poor, below confocal laser scanning microscopy. Here, we propose a straightforward implementation of 2PE image scanning microscopy (2PE-ISM) that, by leveraging our recently introduced single-photon avalanche diode (SPAD) array detector and a novel blind image reconstruction method, is shown to enhance the effective resolution, as well as the overall image quality of 2PE microscopy. With our adaptive pixel reassignment procedure similar to 1.6 times resolution increase is maintained deep into thick semi-transparent samples. The integration of Fourier ring correlation based semi-blind deconvolution is shown to further enhance the effective resolution by a factor of similar to 2 - and automatic background correction is shown to boost the image quality especially in noisy images. Most importantly, our 2PE-ISM implementation requires no calibration measurements or other input from the user, which is an important aspect in terms of day-to-day usability of the technique. (C) 2020 Optical Society of America under the terms of the OSA Open Access Publishing Agreement-
dc.description.sponsorshipH2020 Marie Sklodowska-Curie Actions (AdaptiveSTED, No. 794531); FondsWetenschappelijk Onderzoek (G092915, V429717N); European Research Council (Bright Eyes, No. 818699).-
dc.language.isoen-
dc.publisherOPTICAL SOC AMER-
dc.rights© 2020 Optical Society of America under the terms of the OSA Open Access Publishing Agreement.-
dc.subject.otherFluorescence Microscopy-
dc.subject.otherAdaptive Optics-
dc.subject.otherResolution-
dc.subject.otherSuperresolution-
dc.subject.otherIllumination-
dc.subject.otherEnhancement-
dc.subject.otherDepth-
dc.subject.otherLimit-
dc.subject.otherLive-
dc.subject.otherTool-
dc.titleTwo-photon image-scanning microscopy with SPAD array and blind image reconstruction-
dc.typeJournal Contribution-
dc.identifier.epage2924-
dc.identifier.issue6-
dc.identifier.spage2905-
dc.identifier.volume11-
local.format.pages20-
local.bibliographicCitation.jcatA1-
dc.description.notesVicidomini, G (corresponding author), Ist Italiano Tecnol, Mol Microscopy & Spect, Genoa, Italy.-
dc.description.notesgiuseppe.vicidomini@iit.it-
dc.description.otherVicidomini, G (corresponding author), Ist Italiano Tecnol, Mol Microscopy & Spect, Genoa, Italy giuseppe.vicidomini@iit.it-
local.publisher.place2010 MASSACHUSETTS AVE NW, WASHINGTON, DC 20036 USA-
local.type.refereedRefereed-
local.type.specifiedArticle-
local.type.programmeH2020-
local.relation.h2020794531-
dc.identifier.doi10.1364/BOE.374398-
dc.identifier.pmid32637232-
dc.identifier.isiWOS:000561843300003-
dc.contributor.orcidButtafava, Mauro/0000-0002-5446-8026; Koho, Sami/0000-0003-3927-1687;-
dc.contributor.orcidSheppard, Colin/0000-0002-0792-4607-
dc.identifier.eissn-
local.provider.typewosris-
local.uhasselt.uhpubyes-
local.description.affiliation[Koho, Sami, V; Slenders, Eli; Tortarolo, Giorgio; Castello, Marco; Tcarenkova, Elena; Vicidomini, Giuseppe] Ist Italiano Tecnol, Mol Microscopy & Spect, Genoa, Italy.-
local.description.affiliation[Koho, Sami, V; Tcarenkova, Elena] Univ Turku, Inst Biomed, Dept Cell Biol & Anat, Lab Biophys, Turku, Finland.-
local.description.affiliation[Koho, Sami, V; Tcarenkova, Elena] Med Res Labs, Turku, Finland.-
local.description.affiliation[Slenders, Eli; Ameloot, Marcel] Hasselt Univ, Biomed Res Inst BIOMED, Diepenbeek, Belgium.-
local.description.affiliation[Tortarolo, Giorgio] Univ Genoa, Dipartimento Informat Bioingn Robot & Ingn, Genoa, Italy.-
local.description.affiliation[Buttafava, Mauro; Villa, Federica; Tosi, Alberto] Politecn Milan, Dipartimento Elettron Informaz & Bioingn, Milan, Italy.-
local.description.affiliation[Bianchini, Paolo; Sheppard, Colin J. R.; Diaspro, Alberto] Ist Italiano Tecnol, Nanoscopy, Genoa, Italy.-
local.description.affiliation[Diaspro, Alberto] Univ Genoa, Dipartimento Fis, Genoa, Italy.-
item.contributorKoho, Sami, V-
item.contributorSLENDERS, Eli-
item.contributorTortarolo, Giorgio-
item.contributorCastello, Marco-
item.contributorButtafava, Mauro-
item.contributorVilla, Federica-
item.contributorTcarenkova, Elena-
item.contributorAMELOOT, Marcel-
item.contributorBianchini, Paolo-
item.contributorSheppard, Colin J. R.-
item.contributorDiaspro, Alberto-
item.contributorTosi, Alberto-
item.contributorVicidomini, Giuseppe-
item.fullcitationKoho, Sami, V; SLENDERS, Eli; Tortarolo, Giorgio; Castello, Marco; Buttafava, Mauro; Villa, Federica; Tcarenkova, Elena; AMELOOT, Marcel; Bianchini, Paolo; Sheppard, Colin J. R.; Diaspro, Alberto; Tosi, Alberto & Vicidomini, Giuseppe (2020) Two-photon image-scanning microscopy with SPAD array and blind image reconstruction. In: BIOMEDICAL OPTICS EXPRESS, 11(6), p. 2905-2924.-
item.accessRightsOpen Access-
item.fulltextWith Fulltext-
item.validationecoom 2021-
crisitem.journal.issn2156-7085-
crisitem.journal.eissn2156-7085-
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