Single-shot refractive index slice imaging using spectrally multiplexed optical transfer function reshaping

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dc.contributor.authorLee, Chunghako
dc.contributor.authorHugonnet, Herveko
dc.contributor.authorPark, Juyeonko
dc.contributor.authorLee, Mahn Jaeko
dc.contributor.authorPark, Weisunko
dc.contributor.authorPark, Yongkeunko
dc.date.accessioned2023-06-21T03:01:09Z-
dc.date.available2023-06-21T03:01:09Z-
dc.date.created2023-06-21-
dc.date.created2023-06-21-
dc.date.issued2023-04-
dc.identifier.citationOPTICS EXPRESS, v.31, no.9, pp.13806 - 13816-
dc.identifier.issn1094-4087-
dc.identifier.urihttp://hdl.handle.net/10203/307381-
dc.description.abstractThe refractive index (RI) of cells and tissues is crucial in pathophysiology as a noninvasive and quantitative imaging contrast. Although its measurements have been demon-strated using three-dimensional quantitative phase imaging methods, these methods often require bulky interferometric setups or multiple measurements, which limits the measurement sensitivity and speed. Here, we present a single-shot RI imaging method that visualizes the RI of the in-focus region of a sample. By exploiting spectral multiplexing and optical transfer function engineering, three color-coded intensity images of a sample with three optimized illuminations were simultaneously obtained in a single-shot measurement. The measured intensity images were then deconvoluted to obtain the RI image of the in-focus slice of the sample. As a proof of concept, a setup was built using Fresnel lenses and a liquid-crystal display. For validation purposes, we measured microspheres of known RI and cross-validated the results with simulated results. Various static and highly dynamic biological cells were imaged to demonstrate that the proposed method can conduct single-shot RI slice imaging of biological samples with subcellular resolution.-
dc.languageEnglish-
dc.publisherOptica Publishing Group-
dc.titleSingle-shot refractive index slice imaging using spectrally multiplexed optical transfer function reshaping-
dc.typeArticle-
dc.identifier.wosid000988193100002-
dc.identifier.scopusid2-s2.0-85158016337-
dc.type.rimsART-
dc.citation.volume31-
dc.citation.issue9-
dc.citation.beginningpage13806-
dc.citation.endingpage13816-
dc.citation.publicationnameOPTICS EXPRESS-
dc.identifier.doi10.1364/OE.485559-
dc.contributor.localauthorPark, Yongkeun-
dc.contributor.nonIdAuthorLee, Mahn Jae-
dc.contributor.nonIdAuthorPark, Weisun-
dc.description.isOpenAccessN-
dc.type.journalArticleArticle-
dc.subject.keywordPlusDIFFRACTION TOMOGRAPHY-
dc.subject.keywordPlusCONTRAST-
dc.subject.keywordPlusMICROSCOPY-
dc.subject.keywordPlusCELLS-
dc.subject.keywordPlusQUANTIFICATION-
dc.subject.keywordPlusILLUMINATION-
dc.subject.keywordPlusRESOLUTION-
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