We present a new label-free three-dimensional (3D) microscopy technique, termed transport of intensity diffraction tomography with non-interferometric synthetic aperture (TIDT-NSA). Without resorting to interferometric detection, TIDT-NSA retrieves the 3D refractive index (RI) distribution of biological specimens from 3D intensity-only measurements at various illumination angles, allowing incoherent-diffraction-limited quantitative 3D phase-contrast imaging. The unique combination of z-scanning the sample with illumination angle diversity in TIDT-NSA provides strong defocus phase contrast and better optical sectioning capabilities suitable for high-resolution tomography of thick biological samples. Based on an off-the-shelf bright-field microscope with a programmable light-emitting-diode (LED) illumination source, TIDT-NSA achieves an imaging resolution of 206 nm laterally and 520 nm axially with a high-NA oil immersion objective. We validate the 3D RI tomographic imaging performance on various unlabeled fixed and live samples, including human breast cancer cell lines MCF-7, human hepatocyte carcinoma cell lines HepG2, mouse macrophage cell lines RAW 264.7, Caenorhabditis elegans (C. elegans), and live Henrietta Lacks (HeLa) cells. These results establish TIDT-NSA as a new non-interferometric approach to optical diffraction tomography and 3D label-free microscopy, permitting quantitative characterization of cell morphology and time-dependent subcellular changes for widespread biological and medical applications.

Photonic hook (PH) is a new type of non-evanescent light beam with subwavelength curved structures. It has shown promising applications in super-resolution imaging and has the potential to be used in micromachining, optical trapping, etc. PHs are generally produced by illuminating mesoscale asymmetric particles with optical plane waves. In this work, we used the finite-difference time-domain (FDTD) method to investigate the PH phenomenon under point-source illumination. We found that the PHs can be effectively generated from point-source illuminated patchy particles. By changing the background refractive index, particle diameters and the position and coverage ratio of Ag patches, the characteristics of the PHs can be effectively tuned. Moreover, the structure of the intensity distribution of the light field generated from small and large particles can have an opposite bending direction due to the near-field light-matter interaction.

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Based on a bright‐field microscope with a programmable LED array light source, accelerated Fourier ptychographic diffraction tomography (aFPDT) technique employing a hybrid strategy of sparse annular and multiplexing illuminations was developed to achieve large field‐of‐view and high‐resolution 3D RI tomographic imaging. Compared with previous work, aFPDT enables the reducing of intensity data requirement by more than 40 times and to achieve computational acceleration of 3D tomographic reconstruction. aFPDT has the potential to advance its widespread applications in biomedicine.Further details can be found in the article by Shun Zhou, Jiaji Li, Jiasong Sun, Ning Zhou, Qian Chen, and Chao Zuo (e202100272).image