Literature DB >> 31566889

Label-free spectroscopic tissue characterization using fluorescence excitation-scanning spectral imaging.

Peter F Favreau1, Joshua A Deal2, Bradley Harris3, David S Weber4, Thomas C Rich5, Silas J Leavesley2,5.   

Abstract

Spectral imaging approaches provide new possibilities for measuring and discriminating fluorescent molecules in living cells and tissues. These approaches often employ tunable filters and robust image processing algorithms to identify many fluorescent labels in a single image set. Here, we present results from a novel spectral imaging technology that scans the fluorescence excitation spectrum, demonstrating that excitation-scanning hyperspectral image data can discriminate among tissue types and estimate the molecular composition of tissues. This approach allows fast, accurate quantification of many fluorescent species from multivariate image data without the need of exogenous labels or dyes. We evaluated the ability of the excitation-scanning approach to identify endogenous fluorescence signatures in multiple unlabeled tissue types. Signatures were screened using multi-pass principal component analysis. Endmember extraction techniques revealed conserved autofluorescent signatures across multiple tissue types. We further examined the ability to detect known molecular signatures by constructing spectral libraries of common endogenous fluorophores and applying multiple spectral analysis techniques on test images from lung, liver and kidney. Spectral deconvolution revealed structure-specific morphologic contrast generated from pure molecule signatures. These results demonstrate that excitation-scanning spectral imaging, coupled with spectral imaging processing techniques, provides an approach for discriminating among tissue types and assessing the molecular composition of tissues. Additionally, excitation scanning offers the ability to rapidly screen molecular markers across a range of tissues without using fluorescent labels. This approach lays the groundwork for translation of excitation-scanning technologies to clinical imaging platforms.
© 2019 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Keywords:  endoscopy; hyperspectral; image processing; microscopy; optical biopsy; spectroscopy

Mesh:

Substances:

Year:  2019        PMID: 31566889     DOI: 10.1002/jbio.201900183

Source DB:  PubMed          Journal:  J Biophotonics        ISSN: 1864-063X            Impact factor:   3.207


  4 in total

1.  Development of an endothelial cell-restricted transgenic reporter rat: a resource for physiological studies of vascular biology.

Authors:  Mikhail Alexeyev; Aron M Geurts; Naga S Annamdevula; C Michael Francis; Silas Josiah Leavesley; Thomas C Rich; Mark S Taylor; Mike T Lin; Ron Balczon; Jennifer Michelle Knighten; Diego F Alvarez; Troy Stevens
Journal:  Am J Physiol Heart Circ Physiol       Date:  2020-06-26       Impact factor: 4.733

2.  Microscopy is better in color: development of a streamlined spectral light path for real-time multiplex fluorescence microscopy.

Authors:  Craig M Browning; Samantha Mayes; Samuel A Mayes; Thomas C Rich; Silas J Leavesley
Journal:  Biomed Opt Express       Date:  2022-06-07       Impact factor: 3.562

3.  Comparison of Whiskbroom and Pushbroom darkfield elastic light scattering spectroscopic imaging for head and neck cancer identification in a mouse model.

Authors:  Miriam C Bassler; Mona Stefanakis; Inês Sequeira; Edwin Ostertag; Alexandra Wagner; Jörg W Bartsch; Marion Roeßler; Robert Mandic; Eike F Reddmann; Anita Lorenz; Karsten Rebner; Marc Brecht
Journal:  Anal Bioanal Chem       Date:  2021-11-19       Impact factor: 4.478

4.  Spectrofluorometric Analysis of Autofluorescing Components of Crude Serum from a Rat Liver Model of Ischemia and Reperfusion.

Authors:  Anna C Croce; Andrea Ferrigno; Clarissa Berardo; Giovanni Bottiroli; Mariapia Vairetti; Laura G Di Pasqua
Journal:  Molecules       Date:  2020-03-14       Impact factor: 4.411

  4 in total

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