Abstract

Hyperspectral imaging is highly sought after in many fields including mineralogy and geology, environment and agriculture, astronomy and, importantly, biomedical imaging and biological fluorescence. We developed ultrafast phasor-based hyperspectral snapshot microscopy based on sine/cosine interference filters for biomedical imaging not feasible with conventional hyperspectral detection methods. Current approaches rely on slow spatial or spectral scanning limiting their application in living biological tissues, while faster snapshot methods such as image mapping spectrometry and multispectral interferometry are limited in spatial and/or spectral resolution, are computationally demanding, and imaging devices are very expensive to manufacture. Leveraging light sheet microscopy, phasor-based hyperspectral snapshot microscopy improved imaging speed 10–100 fold which, combined with minimal light exposure and high detection efficiency, enabled hyperspectral metabolic imaging of live, three-dimensional mouse tissues not feasible with other methods. As a fit-free method that does not require any a priori information often unavailable in complex and evolving biological systems, the rule of linear combinations of the phasor could spectrally resolve subtle differences between cell types in the developing zebrafish retina and spectrally separate and track multiple organelles in 3D cultured cells over time. The sine/cosine snapshot method is adaptable to any microscope or imaging device thus making hyperspectral imaging and fit-free analysis based on linear combinations broadly available to researchers and the public.

Hedde et al. demonstrate the use of ultrafast phasor-based hyperspectral snapshot microscopy for biomedical imaging. This technique can improve imaging speed by 10-100 fold and enables 3D hyperspectral imaging of live tissues without using expensive and specialized hyperspectral cameras.

Details

Title
Phasor-based hyperspectral snapshot microscopy allows fast imaging of live, three-dimensional tissues for biomedical applications
Author
Hedde, Per Niklas 1   VIAFID ORCID Logo  ; Cinco Rachel 2 ; Malacrida Leonel 3   VIAFID ORCID Logo  ; Kamaid Andrés 4 ; Gratton Enrico 5   VIAFID ORCID Logo 

 University of California, Laboratory for Fluorescence Dynamics, Irvine, USA (GRID:grid.266093.8) (ISNI:0000 0001 0668 7243); University of California, Department of Pharmaceutical Sciences, Irvine, USA (GRID:grid.266093.8) (ISNI:0000 0001 0668 7243); University of California, Beckman Laser Institute & Medical Clinic, Irvine, USA (GRID:grid.266093.8) (ISNI:0000 0001 0668 7243) 
 University of California, Laboratory for Fluorescence Dynamics, Irvine, USA (GRID:grid.266093.8) (ISNI:0000 0001 0668 7243) 
 Universidad de la República, Departamento de Fisiopatología, Hospital de Clínicas, Facultad de Medicina, Montevideo, Uruguay (GRID:grid.11630.35) (ISNI:0000000121657640); Advanced Bioimaging Unit, Institut Pasteur of Montevideo and Universidad de la República, Montevideo, Uruguay (GRID:grid.11630.35) (ISNI:0000000121657640) 
 Advanced Bioimaging Unit, Institut Pasteur of Montevideo and Universidad de la República, Montevideo, Uruguay (GRID:grid.11630.35) (ISNI:0000000121657640) 
 University of California, Laboratory for Fluorescence Dynamics, Irvine, USA (GRID:grid.266093.8) (ISNI:0000 0001 0668 7243); University of California, Beckman Laser Institute & Medical Clinic, Irvine, USA (GRID:grid.266093.8) (ISNI:0000 0001 0668 7243) 
Publication year
2021
Publication date
2021
Publisher
Nature Publishing Group
e-ISSN
23993642
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2540000878
Copyright
© The Author(s) 2021. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.