Off-axis digital lensless holographic microscopy based on spatially multiplexed interferometry.

digital holographic microscopy digital lensless holographic microscopy label-free imaging off-axis lensless holography phase retrieval quantitative phase imaging spatially multiplexed interferometric microscopy

Journal

Journal of biomedical optics
ISSN: 1560-2281
Titre abrégé: J Biomed Opt
Pays: United States
ID NLM: 9605853

Informations de publication

Date de publication:
Jun 2024
Historique:
received: 29 02 2024
revised: 23 06 2024
accepted: 17 07 2024
medline: 20 8 2024
pubmed: 20 8 2024
entrez: 20 8 2024
Statut: ppublish

Résumé

Digital holographic microscopy (DHM) is a label-free microscopy technique that provides time-resolved quantitative phase imaging (QPI) by measuring the optical path delay of light induced by transparent biological samples. DHM has been utilized for various biomedical applications, such as cancer research and sperm cell assessment, as well as for In addition to the abovementioned advantages, in-line arrangements for DLHM also include the limitation of the twin-image presence, which can restrict accurate QPI. We therefore propose a compact lensless common-path interferometric off-axis approach that is capable of quantitative imaging of fast-moving biological specimens, such as living cells in flow. We suggest lensless spatially multiplexed interferometric microscopy (LESSMIM) as a lens-free variant of the previously reported spatially multiplexed interferometric microscopy (SMIM) concept. LESSMIM comprises a common-path interferometric architecture that is based on a single diffraction grating to achieve digital off-axis holography. From a series of single-shot off-axis holograms, twin-image free and time-resolved QPI is achieved by commonly used methods for Fourier filtering-based reconstruction, aberration compensation, and numerical propagation. Initially, the LESSMIM concept is experimentally demonstrated by results from a resolution test chart and investigations on temporal stability. Then, the accuracy of QPI and capabilities for imaging of living adherent cell cultures is characterized. Finally, utilizing a microfluidic channel, the cytometry of suspended cells in flow is evaluated. LESSMIM overcomes several limitations of in-line DLHM and provides fast time-resolved QPI in a compact optical arrangement. In summary, LESSMIM represents a promising technique with potential biomedical applications for fast imaging such as in imaging flow cytometry or sperm cell analysis.

Identifiants

pubmed: 39161785
doi: 10.1117/1.JBO.29.S2.S22715
pii: 240066SSR
pmc: PMC11331263
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

S22715

Informations de copyright

© 2024 The Authors.

Auteurs

José Ángel Picazo-Bueno (JÁ)

University of Muenster, Biomedical Technology Center, Muenster, Germany.
University of Valencia, Department of Optics, Optometry and Vision Science, Burjassot, Spain.

Steffi Ketelhut (S)

University of Muenster, Biomedical Technology Center, Muenster, Germany.

Jürgen Schnekenburger (J)

University of Muenster, Biomedical Technology Center, Muenster, Germany.

Vicente Micó (V)

University of Valencia, Department of Optics, Optometry and Vision Science, Burjassot, Spain.

Björn Kemper (B)

University of Muenster, Biomedical Technology Center, Muenster, Germany.

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Classifications MeSH