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Jennifer Cauzzo

Publications and source records attributed to Jennifer Cauzzo.

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Label-free chip-based evanescent light scattering super-resolution and superior-contrast optical microscopy (cELS)

Chip-based Evanescent Light Scattering (cELS) utilizes the multiple modes of a high-index contrast optical waveguide for near-field illumination of unlabeled samples, thereby repositioning the highest spatial frequencies of the sample into the far-field. The multiple modes scattering off the sample with different phase differences is engineered to have random spatial distributions within the integration time of the camera, mitigating the coherent speckle noise. This enables label-free superior-contrast imaging of weakly scattering nanosized specimens such as extra-cellular vesicles (EVs) and liposomes, dynamics of living HeLa cells etc. The article explains and validates experimentally the physics behind cELS by demonstrating a multi-moded straight waveguide as a partially coherent light source. For isotropic super-resolution, spatially incoherent light engineered via multiple-arms waveguide chip and intensity-fluctuation based algorithms are used. The proof-of-concept results are demonstrated on 100 nm polystyrene beads and resolution improvement of close to 2X is shown. cELS also realizes (2-10)X more contrast as opposed to conventional imaging techniques. In addition, cELS platform is miniaturized and enables large field-of-view imaging compared to state of the art label-free techniques. cELS holds a potential for label-free super-resolution imaging of nanosized biological specimens at high-throughput.

physics.optics

Fluorescence fluctuations-based super-resolution microscopy techniques: an experimental comparative study

Fluorescence fluctuations-based super-resolution microscopy (FF-SRM) is an emerging field promising low-cost and live-cell compatible imaging beyond the resolution of conventional optical microscopy. A comprehensive overview on how the nature of fluctuations, label density, out-of-focus light, sub-cellular dynamics, and the sample itself influence the reconstruction in FF-SRM is crucial to design appropriate biological experiments. We have experimentally compared several of the recently developed FF-SRM techniques (namely ESI, bSOFI, SRRF, SACD, MUSICAL and HAWK) on widefield fluorescence image sequences of a diverse set of samples (namely liposomes, tissues, fixed and living cells), and on three-dimensional simulated data where the ground truth is available. The simulated microscopy data showed that the different techniques have different requirements for signal fluctuation to achieve their optimal performance. While different levels of signal fluctuations had little effect on the SRRF, ESI and SACD images, image reconstructions from both bSOFI and MUSICAL displayed a substantial improvement in their noise rejection, z-sectioning, and overall super-resolution capabilities.

eess.IV