Siddharth Sivankutty

Single shot polarimetry imaging of multicore fiber

We report an experimental test of single-shot polarimetry applied to the problem of real-time monitoring of the output polarization states in each core within a multicore fiber bundle. The technique uses a stress-engineered optical element, together with an analyzer, and provides a point spread function whose shape unambiguously reveals the polarization state of a point source. We implement this technique to monitor, simultaneously and in real time, the output polarization states of up to 180 single-mode fiber cores in both conventional and polarization-maintaining fiber bundles. We demonstrate also that the technique can be used to fully characterize the polarization properties of each individual fiber core, including eigen-polarization states, phase delay, and diattenuation.

Measurement and compensation of residual group delay in a multi-core fiber for lensless endoscopy

We present a new experimental concept suitable for partially compensating the inter-core group delay dispersion in a multi-core fiber (MCF). First we map out the group delays of all 169 single-mode cores of a MCF using phase-shifting spectral interferometry and find the group delays distributed with standard deviation 123 fs in a 30 cm long MCF. We then detail and apply the compensation scheme based on two wavefront shapers with which we narrow the group delay distribution to 65 fs. These results are relevant for lensless endoscopes employing femtosecond excitation, and we quantify the performance gain in a lensless endoscope with 150 fs laser pulses as excitation and discuss possible generalizations of the concept.

Extended field-of-view in a lensless endoscope using an aperiodic multicore fiber

We investigate lensless endoscopy using coherent beam combining and aperiodic multicore fibers (MCF). We show that diffracted orders, inherent to MCF with periodically arranged cores, dramatically reduce the field-of-view (FoV), and that randomness in MCF core positions can increase the FoV up to the diffraction limit set by a single fiber core, while maintaining a MCF experimental feasibility. We demonstrate experimentally pixelation-free lensless endoscopy imaging over a 120 μm FoV with an aperiodic MCF designed with widely spaced cores. We show that this system is suitable to perform beam scanning imaging by simply applying a tilt to the proximal wavefront.

Ultra-thin rigid endoscope: two-photon imaging through a graded-index multi-mode fiber

Rigid endoscopes like graded-index (GRIN) lenses are known tools in biological imaging, but it is conceptually difficult to miniaturize them. In this letter, we demonstrate an ultra-thin rigid endoscope with a diameter of only 125 μm. In addition, we identify a domain where two-photon endoscopic imaging with fs-pulse excitation is possible. We validate the ultra-thin rigid endoscope consisting of a few cm of graded-index multi-mode fiber by using it to acquire optically sectioned two-photon fluorescence endoscopic images of three-dimensional samples.

Widefield lensless endoscopy with a multicore fiber

We demonstrate pixelation-free real-time widefield endoscopic imaging through an aperiodic multicore fiber (MCF) without any distal opto-mechanical elements or proximal scanners. Exploiting the memory effect in MCFs, the images in our system are directly obtained without any post-processing using a static wavefront correction obtained from a single calibration procedure. Our approach allows for video-rate 3D widefield imaging of incoherently illuminated objects with imaging speed not limited by the wavefront-shaping device refresh rate.

Ultrathin endoscopes based on multicore fibers and adaptive optics: a status review and perspectives.

Abstract. We take stock of the progress that has been made into developing ultrathin endoscopes assisted by wave front shaping. We focus our review on multicore fiber-based lensless endoscopes intended for multiphoton imaging applications. We put the work into perspective by comparing with alternative approaches and by outlining the challenges that lie ahead.

Confocal supercritical angle microscopy for cell membrane imaging

We demonstrate subwavelength sectioning on biological samples with a conventional confocal microscope. This optical sectioning is achieved by the phenomenon of supercritical angle fluorescence, wherein only a fluorophore next to the interface of a refractive index discontinuity can emit propagating components of radiation into the so-called forbidden angles. The simplicity of this technique allows it to be integrated with a high numerical aperture confocal scanning microscope by only a simple modification on the detection channel. Confocal-supercritical angular fluorescence microscopy would be a powerful tool to achieve high-resolution surface imaging, especially for membrane imaging in biological samples.

A straightforward STED-background corrected fitting model for unbiased STED-FCS analyses

Combining stimulated emission depletion and fluorescence correlation spectroscopy (STED-FCS) provides a powerful and sensitive tool for studying the molecular dynamics in live cells with high spatio-temporal resolution. STED-FCS gives access to molecular diffusion characteristic at the nanoscale occurring within short period of times. However due to the incomplete suppression of fluorescence in the STED process, the STED-FCS point spread function (PSF) deviates from a Gaussian shape and challenges the analysis of the auto-correlation curves obtained by FCS. Here, we model the effect of the incomplete fluorescence suppression in STED-FCS experiments and propose a new fitting model improving the accuracy of the diffusion times and average molecule numbers measurements. The implementation of a STED module with pulsed laser source on a commercial confocal/FCS microscope allowed us to apply the STED-background corrected model to fit the STED-FCS measurements. The experimental results are in good accordance with the theoretical analysis both for the number of molecules and the diffusion time which decrease accordingly with the STED power.

Improving endoscopic imaging with disordered multi-core fiber bundles (Conference Presentation)

The periodic arrangement of core positions in multi-core fiber bundles introduces ‘ghost’ artifacts to endoscopic images obtained through them, whether in wide-field imaging (based on either direct imaging or speckle correlations) or in confocal scanning microscopy using wavefront shaping. Here we introduce partially disordered multi-core bundles as a means to overcome these artifacts. The benefits of their use will be discussed in the context of multiphoton scanning microscopy utilizing a spatial light modulator in the proximal end, and in the more general case of widefield imaging. We also show that both numerically and experimentally that the presence of disorder also enables to apply phase retrieval methods to characterize the phase distortion introduced due to propagation in the bundle without the need of an interferometrically stabilized reference. Thus, in addition to overcoming the challenge of ghost artifacts, disordered multi-core fibers have the potential to overcome another challenge, movement-induced phase distortions, by enabling real-time characterization of this phase distortion in reflection mode only via the proximal end.

Phase retrieval in multicore fiber bundles

Multicore fiber bundles are widely used in endoscopy due to their miniature size and their direct imaging capabilities. They have recently been used, in combination with spatial light modulators, in various realizations of endoscopy with little or no optics at the distal end. These schemes require characterization of the relative phase offsets between the different cores, typically done using off-axis holography, thus requiring both an interferometric setup and, typically, access to the distal tip. Here we explore the possibility of employing phase retrieval to extract the necessary phase information. We show that in the noise-free case, disordered fiber bundles are superior for phase retrieval over their periodic counterparts, and demonstrate experimentally accurate retrieval of phase information for up to 10 simultaneously illuminated cores. Thus, phase retrieval is presented as a viable alternative for real-time monitoring of phase distortions in multicore fiber bundles.