NIR-II squeezed light-field microscopy (NIR-II SLIM) is introduced, which optically rotates and compresses multiple perspective views before detection, allowing efficient use of camera pixels while retaining complementary spatial information for three-dimensional reconstruction.
Abstract
High-speed three-dimensional imaging in scattering biological tissues remains challenging because volumetric microscopy generally requires scanning, whereas snapshot light-field approaches divide limited detector pixels among multiple views. This constraint is particularly severe in the second near-infrared window (NIR-II), where InGaAs cameras have small sensor formats and high detector noise. Here we introduce NIR-II squeezed light-field microscopy (NIR-II SLIM), which optically rotates and compresses multiple perspective views before detection, allowing efficient use of camera pixels while retaining complementary spatial information for three-dimensional reconstruction. NIR-II SLIM acquires up to 600 volumes s⁻¹ with a reconstructed lateral sampling grid of 512 × 512 pixels. We use this method for label-free imaging of cardiac dynamics in pigmented late-larval zebrafish, resolving chamber deformation and millisecond-scale atrioventricular-valve motion, and for NIR-II fluorescence imaging of vascular and lymphatic transport in mice. NIR-II SLIM provides a detector-efficient approach for high-speed volumetric imaging of rapid biological dynamics in scattering tissues.
Light-field microscopy enables snapshot volumetric imaging, but its information rate is constrained by both optical encoding and detector readout architecture. Here we develop a task-dependent Fisher-information framework that evaluates optical encoders relative to the detector resource limiting acquisition throughput....
Significance Two-photon microscopy (TPM) is ideally suited for in vivo brain function imaging because of its high resolution and deep tissue penetration. However, conventional TPM is limited by a restricted field-of-view (FOV), an inherent trade-off between the imaging area and temporal resolution, and an insufficient...
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Infrared (IR) microscopy shows substantial potential for label-free tissue imaging in anatomic pathology, providing rich biochemical contrast. However, existing IR imaging technologies are constrained by slow acquisition speeds and limited spatial resolution. Here, we present a rapid, large-field bimodal imaging platfo...
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Light-sheet fluorescence microscopy enables rapid three-dimensional imaging of biological specimens with low phototoxicity and high signal-to-noise ratio, but its imaging depth is limited by optical scattering and absorption in tissue. X-ray light-sheet microscopy, termed Microscopy by Achromatic X-rays With Emission...