TY - JOUR
T1 - Pixelation with Concentration-Encoded Effective Photons for Quantitative Molecular Optical Sectioning Microscopy
AU - Wang, Geng
AU - Iyer, Rishyashring R.
AU - Sorrells, Janet E.
AU - Aksamitiene, Edita
AU - Chaney, Eric J.
AU - Renteria, Carlos A.
AU - Park, Jaena
AU - Shi, Jindou
AU - Sun, Yi
AU - Boppart, Stephen A.
AU - Tu, Haohua
N1 - Publisher Copyright:
© 2024 The Author(s). Laser & Photonics Reviews published by Wiley-VCH GmbH.
PY - 2024/10
Y1 - 2024/10
N2 - Irreproducibility in molecular optical sectioning microscopy has hindered the transformation of acquired digital images from qualitative descriptions to quantitative data. Although numerous tools, metrics, and phantoms have been developed, accurate quantitative comparisons of data from different microscopy systems with diverse acquisition conditions remains a challenge. Here, they develop a simple tool based on an absolute measurement of bulk fluorophore solutions with related Poisson photon statistics, to overcome this obstacle is developed. Demonstrated in a prototypical multiphoton microscope, this tool unifies the unit of pixelated measurement to enable objective comparison of imaging performance across different modalities, microscopes, components/settings, and molecular targets. The application of this tool in live specimens identifies an attractive methodology for quantitative imaging, which rapidly acquires low signal-to-noise frames with either gentle illumination or low-concentration fluorescence labeling.
AB - Irreproducibility in molecular optical sectioning microscopy has hindered the transformation of acquired digital images from qualitative descriptions to quantitative data. Although numerous tools, metrics, and phantoms have been developed, accurate quantitative comparisons of data from different microscopy systems with diverse acquisition conditions remains a challenge. Here, they develop a simple tool based on an absolute measurement of bulk fluorophore solutions with related Poisson photon statistics, to overcome this obstacle is developed. Demonstrated in a prototypical multiphoton microscope, this tool unifies the unit of pixelated measurement to enable objective comparison of imaging performance across different modalities, microscopes, components/settings, and molecular targets. The application of this tool in live specimens identifies an attractive methodology for quantitative imaging, which rapidly acquires low signal-to-noise frames with either gentle illumination or low-concentration fluorescence labeling.
KW - POISSON photon statistics
KW - fluorescence microscopy
KW - multiphoton microscopy
KW - quantitative microscopy
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U2 - 10.1002/lpor.202400031
DO - 10.1002/lpor.202400031
M3 - Article
AN - SCOPUS:85197378039
SN - 1863-8880
VL - 18
JO - Laser and Photonics Reviews
JF - Laser and Photonics Reviews
IS - 10
M1 - 2400031
ER -