Two-photon image-scanning microscopy with SPAD array and blind image reconstruction

dc.contributor.authorSami V. Koho
dc.contributor.authorEli Slenders
dc.contributor.authorGiorgio Tortarolo
dc.contributor.authorMarco Castello
dc.contributor.authorMauro Buttafava
dc.contributor.authorFederica Villa
dc.contributor.authorElena Tcarenkova
dc.contributor.authorMarcel Ameloot
dc.contributor.authorPaolo Bianchini
dc.contributor.authorColin J. R. Sheppard
dc.contributor.authorAlberto Diaspro
dc.contributor.authorAlberto Tosi
dc.contributor.authorGiuseppe Vicidomini
dc.contributor.organizationfi=biolääketieteen laitos|en=Institute of Biomedicine|
dc.contributor.organization-code1.2.246.10.2458963.20.77952289591
dc.contributor.organization-code2607100
dc.converis.publication-id48978703
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/48978703
dc.date.accessioned2022-10-28T13:50:43Z
dc.date.available2022-10-28T13:50:43Z
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.format.pagerange2905
dc.format.pagerange2924
dc.identifier.jour-issn2156-7085
dc.identifier.olddbid184696
dc.identifier.oldhandle10024/167790
dc.identifier.urihttps://www.utupub.fi/handle/11111/51290
dc.identifier.urnURN:NBN:fi-fe2021042823854
dc.language.isoen
dc.okm.affiliatedauthorKoho, Sami
dc.okm.affiliatedauthorTcarenkova, Elena
dc.okm.discipline3111 Biomedicineen_GB
dc.okm.discipline3111 Biolääketieteetfi_FI
dc.okm.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherOPTICAL SOC AMER
dc.publisher.countryUnited Statesen_GB
dc.publisher.countryYhdysvallat (USA)fi_FI
dc.publisher.country-codeUS
dc.relation.doi10.1364/BOE.374398
dc.relation.ispartofjournalBiomedical Optics Express
dc.relation.issue6
dc.relation.volume11
dc.source.identifierhttps://www.utupub.fi/handle/10024/167790
dc.titleTwo-photon image-scanning microscopy with SPAD array and blind image reconstruction
dc.year.issued2020

Tiedostot

Näytetään 1 - 1 / 1
Ladataan...
Name:
Koho_et_al_2020.pdf
Size:
10.52 MB
Format:
Adobe Portable Document Format
Description:
Publisher's PDF