image: Time-gated light-sheet in vivo imaging system. view more
Credit: OEA
A new publication from Opto-Electronic Advances, 10.29026/oea.2023.220105 discusses deep learning enhanced NIR-II volumetric imaging of whole mice vasculature.
In vivo small animal fluorescence imaging is widely used in oncology, drugs, antibodies, nanomaterials, inflammation, immune diseases, gene therapy, apoptosis, and other research fields because of its advantages such as in vivo real-time imaging observation of labeled animal tissues or exogenous drugs. This system allows for the long-term follow-up of the growth, metastasis, and drug treatment process of tumors in living animals, the development process of infectious diseases, inflammation and bone damage repair, the expression process of specific genes, and the metabolism process of nanomedicine in the organism. The system is also an imaging platform for the design and optimization of various fluorescent materials and biological probes.
Near-infrared II (NIR-II: 1000-1700 nm) is a longer wavelength photon than visible light and NIR-I light. It is less scattered in biological tissues and has lower background interference from biological tissue autofluorescence. With the development of NIR-II photoluminescent probes and supporting cameras and other equipment, the application of NIR-II fluorescence in vivo functional imaging has become a research hotspot. However, current NIR-II in vivo imaging systems are still based on planar imaging obtained with industrial lenses, which can obtain millimeter-depth fluorescence imaging but cannot reflect three-dimensional depth information. In addition, mice are far away from the lens, and the imaging resolution is low. The effect of tissue scattering still exists. Therefore, the development of deep, high-resolution, spatial three-dimensional, high-contrast in vivo imaging systems has become an important development direction for in vivo fluorescence imaging of small animals.
Light-sheet fluorescence microscopy imaging is a three-dimensional imaging technique applied to cells, organoids, and small embryos that allows for rapid three-dimensional imaging of biological samples. In order to achieve deep 3D in vivo imaging with NIR-II fluorescence, improve imaging resolution, and reduce the influence of fluorescence scattering and tissue autofluorescence, the team led by academician Dayong Jin from Southern University of Science and Technology prepared a NIR-II probe with rare earth nanoparticles to detect fluorescence with a peak of about 1530 nm. They first introduced light-sheet imaging into the field of adult whole mouse in vivo imaging. The team used time-gating technology to reduce thermal effects and average laser power. They also enlarged the numerical aperture of imaging by coupling imaging with dual industrial lenses (see Figure 1) and developed a vascular enhancement algorithm based on deep learning to improve imaging contrast. These advancements enabled high-resolution whole-mouse vascular network imaging in the NIR-II region with deep 3D in vivo imaging (see Figure 2).
This study achieved clear resolution of blood vessels in deep tissue with NIR-II body imaging through the synergistic use of time-gated imaging, light sheet scanning, and deep learning algorithms. These techniques effectively reduced the effects of laser scattering and out-of-focus background noise. The 3D in vivo imaging system successfully reconstructed the full length of 527.7 mm of blood vessels in the macroscopic whole mouse subcutaneous 2 mm depth range. The smallest resolvable vessel diameter was up to 100 µm, and the depth resolution was 100 µm. This technique fills the gap between conventional microscopic imaging and macroscopic imaging, providing the possibility of 3D whole-body pathology model research. The system rapidly acquires massive amounts of information and can analyze microscopic details of macroscopic regions of interest, such as the transport processes of cancer cells in blood vessels, in the context of the complete human body. The new generation of NIR-II 3D in vivo deep HD imaging offers significant advantages over current tissue transparency techniques used to avoid scattering effects.
Keywords: NIR-II fluorescence / time-gated / light sheet illumination / deep learning / vessel enhancement / 3D imaging
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In early 2019, Academician Jin Dayong established the University of Science and Technology Sydney-South University of Science and Technology Joint Research Center for Materials and Instrumentation in Biomedical Sciences at the University of Southern Technology, which is dedicated to the development of advanced biomedical technologies, focusing on the design of new materials, the self-development of medical instruments and the integration of precision disease diagnosis technologies. In the past five years, Dr. Jin has published sixteen original reviews in Nature and its sub-journals as corresponding author and has so far published more than 220 academic papers with more than 11,000 citations and an H-Index of 52. He has been invited to present at many international conferences such as SPIE, CYTO, etc. He has served as an associate editor of many international journals such as Light Science & Applications (2nd in Optics), Cytometry A, Journal of Luminescence, and Opto-Electronic Advances, Journal of Rare Earths and Science China Materials, and as an editorial board member of Nature, Nature Photonics, Nature Nanotechnology, Nature Communication, Chemical Society Reviews, Scientific Reports, Advanced Materials, Advanced Functional Materials, Nano Letters, ACS Nano, Journal of Biomedical Optics, Optics Letters, Small, Nanoscale, Chemical Science, etc. Reviewer of Analytical Chemistry and other journals.
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Article reference Wu ST, Yang ZC, Ma CG, Zhang X, Mi C et al. Deep learning enhanced NIR-II volumetric imaging of whole mice vasculature. Opto-Electron Adv 6, 220105 (2023). doi: 10.29026/oea.2023.220105
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