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Pilhan Kim

Publications and source records attributed to Pilhan Kim.

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Programmable spatial coherence tomography: diffraction-limited three-dimensional reflection imaging under modulated monochromatic illumination

Depth sectioning in reflection microscopy has predominantly relied on temporal coherence gating. Here we show that volumetric reflection tomography at diffraction-limited resolution can be achieved under monochromatic illumination by engineering spatial, rather than temporal, coherence. In programmable spatial coherence tomography (PSCT), a sequence of pupil-coded illumination patterns with angular-spectrum diversity generates measurement redundancy enabling the system to calibrate itself, jointly retrieving aberrations, illumination profiles, and sample motion without guide stars or modal priors. We demonstrate label-free volumetric imaging of thick human tissues, organoids, frequency-resolved dynamic contrast, and high-resolution in vivo brain imaging through a cranial window. These results position PSCT as an alternative to temporal coherence based reflection imaging in complex biological systems.

physics.optics

Holographic intravital microscopy for 2-D and 3-D imaging intact circulating blood cells in microcapillaries of live mice

Intravital microscopy is an essential tool that reveals behaviours of live cells under conditions close to natural physiological states. So far, although various approaches for imaging cells in vivo have been proposed, most require the use of labelling and also provide only qualitative imaging information. Holographic imaging approach based on measuring the refractive index distributions of cells, however, circumvent these problems and offer quantitative and label-free imaging capability. Here, we demonstrate in vivo two- and three-dimensional holographic imaging of circulating blood cells in intact microcapillaries of live mice. The measured refractive index distributions of blood cells provide morphological and biochemical properties including three-dimensional cell shape, haemoglobin concentration, and haemoglobin contents at the individual cell level. With the present method, alterations in blood flow dynamics in live healthy and sepsis-model mouse were also investigated.

physics.bio-ph