arXiv subjects

Mikolaj Rogalski

Publications and source records attributed to Mikolaj Rogalski.

8 recordsLinked to original sources

arXiv2026

Hybrid spectral-spatial domain registration for nanometric tracking in digital in-line holographic microscopy

Digital in-line holographic microscopy enables label-free tracking and metrology, but achieving nanometric sub-pixel displacement accuracy over a wide capture range remains challenging. Frequency-domain registration based on the discrete Fourier transform (DFT) is globally stable and tolerant to large shifts, yet it suffers from sub-pixel quantization and interpolation artifacts that limit precision near zero displacement. In contrast, spatial-gradient refinement such as Lucas-Kanade (LK) can reach very high sub-pixel accuracy, but it is strongly initialization-limited and prone to divergence outside a narrow convergence basin. Here we propose a Hybrid Spectral-Spatial Domain (HSSD) framework that resolves this trade-off by combining the global robustness of a DFT-based coarse estimator with LK refinement of the residual motion. The DFT stage provides reliable initialization and substantially extends the capture range, while the LK stage suppresses the precision floor by reducing interpolation and quantization errors characteristic of standalone frequency-domain methods. We validate HSSD using numerical simulations and experiments in a transmission in-line holographic imaging system, achieving nanoprecision displacement measurement and stable tracking across a wide range of displacements and defocusing conditions. This hybrid strategy enables reliable nanometric localization in regimes where standalone DFT or LK methods either fail to converge or saturate in accuracy.

physics.optics↗

arXiv2026

Near-infrared lensless holographic microscopy on a visible sensor enables label-free high-throughput imaging in strong scattering

Lensless digital holographic microscopy (LDHM) relies on interference between an unscattered reference wave and a weakly scattered object wave - an assumption that rapidly fails in turbid samples under multiple scattering. To overcome this limitation, we present near-infrared LDHM (NIR-LDHM), a in-line holographic platform that operates up to the silicon cutoff (~1100 nm) using a conventional board-level CMOS sensor designed for visible (VIS) imaging. Using tissue-mimicking milk scattering layers and calibrated resolution targets, we quantify reconstruction performance versus wavelength, scattering strength, and sample-sensor distance. NIR-LDHM maintains resolvable features through scattering layers up to ~1.4 mm, whereas visible regime fails to resolve features below ~350 um. Importantly, despite a detector quantum efficiency of only 0.19% at 1100 nm, robust reconstructions are obtained under low-photon-budget conditions. We further identify advantageous mechanism by which increasing the sample-sensor distance from ~3 to 12 mm improves lateral resolution by twofold under strong scattering. Finally, we demonstrate wide-field, label-free amplitude-phase imaging of uncleared mouse tissues, resolving internal structure in brain and liver slices up to ~250 um and ~60 um, respectively. By extending lensless complex-field microscopy into strongly scattering regimes with minimal hardware changes, this work has relevance to computational imaging through complex media and biophotonics.

physics.optics↗

arXiv2025

High Space-bandwidth Product Label-free Examination of iPSC-derived Brain Organoids via Fourier Ptychographic Microscopy

Fourier ptychographic microscopy (FPM) is a promising quantitative phase imaging technique that enables high-resolution, label-free imaging over a large field-of-view. Here, we present the first application of FPM for the quantitative analysis of human brain organoid slices, providing a powerful, cost-effective, and label-free enhancement to the current gold-standard fluorescence microscopy. Brain organoids, prepared as thin (5 micrometer) slices, were imaged with a custom-built FPM system consisting of a standard light microscope (4x, 0.2 NA objective) and a 7x7 LED array. This configuration achieved a synthetic numerical aperture of 0.54 and a spatial resolution of approximately 488 nm across an area of 2.077 x 3.65 mm. Fluorescence microscopy was used in parallel for neurons, astrocytes, and nuclei labeling, providing rich fluorescence imaging. Moreover, we designed an automated method to merge classical resolution fluorescence images to visualize the whole brain organoid and align it with the numerically increased space-bandwidth product FPM image. The provided alignment method enables rich phase-fluorescence correlative imaging. Based on the segmentation performed on the stitched fluorescence images, we devised a quantitative phase analysis revealing a higher mean optical thickness of the nuclei versus astrocytes and neurons. Notably, nuclei located in neurogenic regions consistently exhibited significantly higher phase values (optical path difference) compared to nuclei elsewhere, suggesting cell-type-specific biophysical signatures. The label-free, quantitative, and high-throughput capabilities of the FPM approach demonstrated here make it a powerful and accessible tool for future structural and functional studies of whole-section brain organoid development and disease modeling studies.

physics.med-ph↗

arXiv2025

Low-dose Chemically Specific Bioimaging via Deep-UV Lensless Holographic Microscopy on a Standard Camera

Deep-ultraviolet (DUV) microscopy can provide label-free biochemical contrast by exploiting the intrinsic absorption of nucleic acids, proteins and lipids, offering chemically specific morphological information that complements structural optical thickness contrast from phase-sensitive imaging. However, existing DUV microscopes typically rely on specialized optics and DUV-sensitive cameras, which restrict field of view, increase system complexity and cost, and often require high illumination doses that risk photodamage. Here, we report a low-dose deep-UV lensless holographic microscopy platform that uses standard board-level CMOS sensors designed for visible light, eliminating all imaging optics and dedicated DUV detectors. Our system achieves large field-of-view (up to 116 mm2) DUV imaging with low illumination and label-free phase and chemically specific amplitude contrast. A specialized defocus/wavelength diverse pixel super-resolution reconstruction with total-variation regularization and robust autofocusing halves the effective sensor pixel pitch and yields down to 870 nm lateral resolution. We demonstrate chemically specific, label-free bioimaging on challenging specimens, including Saccharomyces cerevisiae, extracellular vesicles and unstained mouse liver tissue. In liver sections, imaging at λ = 330 nm reveals lipid- and retinoid-rich accumulations that co-localize with Oil Red O staining, enabling label-free identification of hepatic stellate (Ito) cells. This combination of low-dose operation, chemically specific contrast and standard CMOS hardware establishes DUV lensless holographic microscopy as a practical and scalable route to high-content submicron-resolution whole-slide preparation-free bioimaging without exogenous labels.

physics.optics↗

arXiv2025

Gigavoxel-Scale Multiple-Scattering-Aware Lensless Holotomography

Holotomography (HT) has revolutionized quantitative label-free 3D imaging, yet conventional lens-based implementations are fundamentally constrained in field-of-view (FOV) and imaging depth, limiting their utility for critical high-throughput applications in material and life sciences. Lensless HT (LHT) offers a promising alternative for large-volume examination, however existing approaches fail to accurately reconstruct highly scattering samples over extended depths, which remains a critical challenge in optical imaging field. Here, we introduce a gigavoxel-scale, multiple-scattering-aware LHT with a large FOV (surpassing 0.6 cm2), millimeter-scale axial range and pixel level (~2.4 micron) resolution. Our approach leverages a multi-wavelength, oblique-illumination hologram reconstruction and a robust, automatic illumination angle calibration, which are necessary for precise large-volume 3D holographic reconstruction. Moreover, we propose optimization-driven multi-slice tomographic framework to accurately capture multiple-scattering effects outperforming first order Born/Rytov-based inversions. To rigorously validate our method, we reconstruct bespoke multi-layer two-photon polymerized test structure over a 1.7 mm imaging depth and 25 mm2 FOV, yielding an unprecedented 3D space-bandwidth product exceeding a gigavoxel level. Furthermore, we demonstrate for the first time on-chip label-free imaging of entire 500-micron-thick tissue slice of optically-cleared mouse brain. With the proposed method, we aim to unlock powerful new capabilities for large-scale, quantitative, label-free 3D imaging across biomedicine, neuroscience, material sciences and beyond.

physics.optics↗

arXiv2023

DeepOrientation: convolutional neural network for fringe pattern orientation map estimation

Fringe pattern based measurement techniques are the state-of-the-art in full-field optical metrology. They are crucial both in macroscale, e.g., fringe projection profilometry, and microscale, e.g., label-free quantitative phase microscopy. Accurate estimation of the local fringe orientation map can significantly facilitate the measurement process on various ways, e.g., fringe filtering (denoising), fringe pattern boundary padding, fringe skeletoning (contouring/following/tracking), local fringe spatial frequency (fringe period) estimation and fringe pattern phase demodulation. Considering all of that the accurate, robust and preferably automatic estimation of local fringe orientation map is of high importance. In this paper we propose novel numerical solution for local fringe orientation map estimation based on convolutional neural network and deep learning called DeepOrientation. Numerical simulations and experimental results corroborate the effectiveness of the proposed DeepOrientation comparing it with the representative of the classical approach to orientation estimation called combined plane fitting/gradient method. The example proving the effectiveness of DeepOrientation in fringe pattern analysis, which we present in this paper is the application of DeepOrientation for guiding the phase demodulation process in Hilbert spiral transform. In particular, living HeLa cells quantitative phase imaging outcomes verify the method as an important asset in label-free microscopy.

eess.IV↗

arXiv2023

Single-shot experimental-numerical twin-image removal in lensless digital holographic microscopy

Lensless digital holographic microscopy (LDHM) offers very large field-of-view label-free imaging crucial, e.g., in high-throughput particle tracking and biomedical examination of cells and tissues. Compact layouts promote point-of-case and out-of-laboratory applications. The LDHM, based on the Gabor in-line holographic principle, is inherently spoiled by the twin-image effect, which complicates the quantitative analysis of reconstructed phase and amplitude maps. Popular family of solutions consists of numerical methods, which tend to minimize twin-image upon iterative process based on data redundancy. Additional hologram recordings are needed, and final results heavily depend on the algorithmic parameters, however. In this contribution we present a novel single-shot experimental-numerical twin-image removal technique for LDHM. It leverages two-source off-axis hologram recording deploying simple fiber splitter. Additionally, we introduce a novel phase retrieval numerical algorithm specifically tailored to the acquired holograms, that provides twin-image-free reconstruction without compromising the resolution. We quantitatively and qualitatively verify proposed method employing phase test target and cheek cells biosample. The results demonstrate that the proposed technique enables low-cost, out-of-laboratory LDHM imaging with enhanced precision, achieved through the elimination of twin-image errors. This advancement opens new avenues for more accurate technical and biomedical imaging applications using LDHM, particularly in scenarios where cost-effective and portable imaging solutions are desired.

physics.optics↗

arXiv2022

Tailoring 2D Fast Iterative Filtering algorithm for low-contrast optical fringe pattern preprocessing

Retrieving object phase from the optical fringe pattern is a critical task in quantitative phase imaging and often requires appropriate image preprocessing (background and noise minimization), especially when retrieving phase from the single-shot fringe pattern image. In this article, for the first time, we propose to adapt the 2D Fast Iterative Filtering (FIF) method for fringe pattern decomposition and develop a novel version of FIF called the 2D fringe pattern Fast Iterative Filtering (fpFIF2), that is tailored for fringe pattern preprocessing. We show the positive influence of fpFIF2 onto fringe pattern filtering comparing to the previous 2D FIF implementation regarding processing speed, quality, and usage comfortability. We also compare the fpFIF2 with other state-of-the-art fringe pattern filtering methods in terms of aiding the Hilbert spiral transform method in phase retrieval. Employing numerical simulations and experimental fringe analysis, we prove that fpFIF2 outperforms reference methods, especially in terms of low-fringe-contrast phase reconstruction quality and decomposition time.

physics.optics↗