TY - JOUR
T1 - Compressive hyperspectral microscopy for cancer detection
AU - Oiknine, Yaniv
AU - Abuleil, Marwan
AU - Brozgol, Eugene
AU - August, Isaac Y.
AU - Barshack, Iris
AU - Abdulhalim, Ibrahim
AU - Garini, Yuval
AU - Stern, Adrian
N1 - Publisher Copyright:
© The Authors. Published by SPIE under a Creative Commons Attribution 4.0 International License.
PY - 2023/9/1
Y1 - 2023/9/1
N2 - Significance: Hyperspectral microscopy grants the ability to characterize unique properties of tissues based on their spectral fingerprint. The ability to label and measure multiple molecular probes simultaneously provides pathologists and oncologists with a powerful tool to enhance accurate diagnostic and prognostic decisions. As the pathological workload grows, having an objective tool that provides companion diagnostics is of immense importance. Therefore, fast whole-slide spectral imaging systems are of immense importance for automated cancer prognostics that meet current and future needs. Aim: We aim to develop a fast and accurate hyperspectral microscopy system that can be easily integrated with existing microscopes and provide flexibility for optimizing measurement time versus spectral resolution. Approach: The method employs compressive sensing (CS) and a spectrally encoded illumination device integrated into the illumination path of a standard microscope. The spectral encoding is obtained using a compact liquid crystal cell that is operated in a fast mode. It provides time-efficient measurements of the spectral information, is modular and versatile, and can also be used for other applications that require rapid acquisition of hyperspectral images. Results: We demonstrated the acquisition of breast cancer biopsies hyperspectral data of the whole camera area within ~1 s. This means that a typical 1 × 1 cm2 biopsy can be measured in ~10 min. The hyperspectral images with 250 spectral bands are reconstructed from 47 spectrally encoded images in the spectral range of 450 to 700 nm. Conclusions: CS hyperspectral microscopy was successfully demonstrated on a common labmicroscope formeasuring biopsies stained with themost common stains, such as hematoxylin and eosin. The high spectral resolution demonstrated here in a rather short time indicates the ability to use it further for coping with the highly demanding needs of pathological diagnostics, both for cancer diagnostics and prognostics.
AB - Significance: Hyperspectral microscopy grants the ability to characterize unique properties of tissues based on their spectral fingerprint. The ability to label and measure multiple molecular probes simultaneously provides pathologists and oncologists with a powerful tool to enhance accurate diagnostic and prognostic decisions. As the pathological workload grows, having an objective tool that provides companion diagnostics is of immense importance. Therefore, fast whole-slide spectral imaging systems are of immense importance for automated cancer prognostics that meet current and future needs. Aim: We aim to develop a fast and accurate hyperspectral microscopy system that can be easily integrated with existing microscopes and provide flexibility for optimizing measurement time versus spectral resolution. Approach: The method employs compressive sensing (CS) and a spectrally encoded illumination device integrated into the illumination path of a standard microscope. The spectral encoding is obtained using a compact liquid crystal cell that is operated in a fast mode. It provides time-efficient measurements of the spectral information, is modular and versatile, and can also be used for other applications that require rapid acquisition of hyperspectral images. Results: We demonstrated the acquisition of breast cancer biopsies hyperspectral data of the whole camera area within ~1 s. This means that a typical 1 × 1 cm2 biopsy can be measured in ~10 min. The hyperspectral images with 250 spectral bands are reconstructed from 47 spectrally encoded images in the spectral range of 450 to 700 nm. Conclusions: CS hyperspectral microscopy was successfully demonstrated on a common labmicroscope formeasuring biopsies stained with themost common stains, such as hematoxylin and eosin. The high spectral resolution demonstrated here in a rather short time indicates the ability to use it further for coping with the highly demanding needs of pathological diagnostics, both for cancer diagnostics and prognostics.
KW - cancer detection
KW - compressive sensing
KW - digital pathology
KW - hyperspectral imaging
KW - liquid crystal modulators
KW - microscopy
UR - http://www.scopus.com/inward/record.url?scp=85170485592&partnerID=8YFLogxK
U2 - 10.1117/1.JBO.28.9.096502
DO - 10.1117/1.JBO.28.9.096502
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C2 - 37692564
AN - SCOPUS:85170485592
SN - 1083-3668
VL - 28
JO - Journal of Biomedical Optics
JF - Journal of Biomedical Optics
IS - 9
M1 - 096502
ER -