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Jolanta Mierzejewska

Publications and source records attributed to Jolanta Mierzejewska.

3 recordsLinked to original sources

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↗

Doubling the field of view and eliminating the replica overlap problem in common-path shearing quantitative phase imaging

Quantitative phase imaging (QPI) enables label-free, high-contrast visualization of transparent specimens, but its common implementation in off-axis digital holographic microscopy (DHM) requires a separate reference beam, which increases system complexity and sensitivity to noise and vibrations. Common-path shearing DHMs overcome these drawbacks by eliminating the reference arm, yet they suffer from sheared object beam (replica) overlap, as both interfering sheared beams traverse the sample and generate superimposed phase images. This limits their use to sparse objects only. Here we introduce R2D-QPI, a method that numerically decouples object and replica fields of view through controlled shear scanning. The method analytically separates overlapped phase images and effectively doubles the imaged area, requiring only two measurements. We experimentally validate the approach on a phase resolution test target, yeast cells, and human thyroid tissue slices, demonstrating accurate reconstruction even in highly confluent samples with strong object-replica overlap. The results establish R2D-QPI as a robust and versatile solution for common-path QPI, enabling wide-field, label-free phase imaging with minimal data acquisition and strong potential for applications in biological and medical microscopy.

physics.optics↗

Speckle suppression in digital in-line holographic microscopy through liquid crystal dynamic scattering

We demonstrate speckle noise reduction in an in-line holographic imaging system using a Zwitterion-doped liquid crystal dynamic scatterer (LCDS) cell diffuser. Integrated into a minimally modified bright-field microscope, the LCDS actively modulates system's spatial coherence. The proposed solution suppresses coherent artifacts without introducing bulky moving parts, while enhancing image resolution and preserving overall system simplicity. Quantitative performance tested on a phase and amplitude test targets, as well as phase-amplitude biological sample, shows significant noise reduction and methods versatility. Though validated in a holographic in-line setup, the approach is applicable to other imaging techniques requiring compact, vibration-free speckle suppression.

physics.optics↗