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Autori principali: Jia, Danchen, Dong, Dashan, Li, Tongyu, Zong, Haonan, Zhu, Jiabei, Teng, Xinyan, Tian, Lei, Cheng, Ji-Xin
Natura: Preprint
Pubblicazione: 2025
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Accesso online:https://arxiv.org/abs/2512.24375
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author Jia, Danchen
Dong, Dashan
Li, Tongyu
Zong, Haonan
Zhu, Jiabei
Teng, Xinyan
Tian, Lei
Cheng, Ji-Xin
author_facet Jia, Danchen
Dong, Dashan
Li, Tongyu
Zong, Haonan
Zhu, Jiabei
Teng, Xinyan
Tian, Lei
Cheng, Ji-Xin
contents Three-dimensional molecular imaging of living cells is essential for unraveling cellular metabolism and response to therapies. However, existing volumetric methods, including fluorescence microscopy and quantitative phase imaging, either require fluorescent labels or lack chemical specificity. Mid-infrared (mid-IR) photothermal microscopy provides label-free spectroscopic contrast with sub-micrometer resolution but is limited by slow acquisition rates, precluding 3D live-cell studies. Here, we present a photothermal relaxation intensity diffraction tomography (PRIDT) system that encodes mid-IR absorption induced refractive index change via a photothermal relaxation scheme and recovers it through intensity diffraction tomography. PRIDT achieves video-rate volumetric chemical imaging with up to 15 Hz per wavelength and offers lateral and axial resolutions of 264 nm and 1.12 um over a volumetric field of view of 50x50x10 um3. We showcase high-speed PRIDT imaging of protein and lipid metabolism in ovarian cancer cells and lipid-droplet dynamics in live cells. PRIDT opens new avenues for rapid, quantitative, three-dimensional molecular imaging in living systems.
format Preprint
id arxiv_https___arxiv_org_abs_2512_24375
institution arXiv
publishDate 2025
record_format arxiv
spellingShingle Mid-Infrared Photothermal Relaxation Intensity Diffraction Tomography for Video-rate Volumetric Chemical Imaging
Jia, Danchen
Dong, Dashan
Li, Tongyu
Zong, Haonan
Zhu, Jiabei
Teng, Xinyan
Tian, Lei
Cheng, Ji-Xin
Optics
Three-dimensional molecular imaging of living cells is essential for unraveling cellular metabolism and response to therapies. However, existing volumetric methods, including fluorescence microscopy and quantitative phase imaging, either require fluorescent labels or lack chemical specificity. Mid-infrared (mid-IR) photothermal microscopy provides label-free spectroscopic contrast with sub-micrometer resolution but is limited by slow acquisition rates, precluding 3D live-cell studies. Here, we present a photothermal relaxation intensity diffraction tomography (PRIDT) system that encodes mid-IR absorption induced refractive index change via a photothermal relaxation scheme and recovers it through intensity diffraction tomography. PRIDT achieves video-rate volumetric chemical imaging with up to 15 Hz per wavelength and offers lateral and axial resolutions of 264 nm and 1.12 um over a volumetric field of view of 50x50x10 um3. We showcase high-speed PRIDT imaging of protein and lipid metabolism in ovarian cancer cells and lipid-droplet dynamics in live cells. PRIDT opens new avenues for rapid, quantitative, three-dimensional molecular imaging in living systems.
title Mid-Infrared Photothermal Relaxation Intensity Diffraction Tomography for Video-rate Volumetric Chemical Imaging
topic Optics
url https://arxiv.org/abs/2512.24375