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Register a new userVideo-rate dual-modal forward-viewing photoacoustic and fluorescence endo-microscopy through a multimode fibre
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Multimode fibres are becoming increasingly attractive in optical endoscopy as they promise to enable unparalleled miniaturisation, spatial resolution and cost as compared to conventional fibre bundle-based counterpart. However, achieving high-speed imaging through a multimode fibre (MMF) based on wavefront shaping has been challenging due to the use of liquid crystal spatial light modulators with low frame rates. In this work, we report the development of a video-rate dual-modal forward-viewing photoacoustic (PA) and fluorescence endo-microscopy probe based on a MMF and a high-speed digital micromirror device (DMD). Light transmission characteristics through the fibre were characterised with a real-valued intensity transmission matrix algorithm, and subsequently, optimal binary patterns were calculated to focus light through the fibre with wavefront shaping. Raster-scanning of a tightly focused beam (1.5 {mu}m diameter) at the distal end of the fibre was performed for imaging. With the DMD running at 10 kHz, the PA imaging speed and spatial resolution of were controlled by varying the scanning step size, ranging from 1 to 25 frames per second (fps) and from 1.7 to 3 {mu}m, respectively, over a field-of-view of 50 {mu}m x 50 {mu}m. High-resolution PA images of carbon fibres, and mouse red blood cells were acquired through a MMF with high image fidelity at unprecedented speed with MMF-based PA endoscope. The capability of dual-modal PA and fluorescence imaging was demonstrated by imaging phantoms comparing carbon fibres and fluorescent microspheres. We anticipate that with further miniaturisation of the ultrasound detector, this probe could be integrated into a medical needle to guide minimally invasive procedures in several clinical contexts including tumour biopsy and nerve blocks.
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Reconfigurable quantum circuits are fundamental building blocks for the implementation of scalable quantum technologies. Their implementation has been pursued in linear optics through the engineering of sophisticated interferometers. While such optical networks have been successful in demonstrating the control of small-scale quantum circuits, scaling up to larger dimensions poses significant challenges. Here, we demonstrate a potentially scalable route towards reconfigurable optical networks based on the use of a multimode fibre and advanced wavefront-shaping techniques. We program networks involving spatial and polarisation modes of the fibre and experimentally validate the accuracy and robustness of our approach using two-photon quantum states. In particular, we illustrate the reconfigurability of our platform by emulating a tunable coherent absorption experiment. By demonstrating reliable reprogrammable linear transformations, with the prospect to scale, our results highlight the potential of complex media driven by wavefront shaping for quantum information processing.
Using the shifted-excitation Raman difference spectroscopy technique and an optical fibre featuring a negative curvature excitation core and a coaxial ring of high numerical aperture collection cores, we have developed a portable, background and fluorescence free, endoscopic Raman probe. The probe consists of a single fibre with a diameter of less than 0.25 mm packaged in a sub-millimetre tubing, making it compatible with standard bronchoscopes. The Raman excitation light in the fibre is guided in air and therefore interacts little with silica, enabling an almost background free transmission of the excitation light. In addition, we used the shifted-excitation Raman difference spectroscopy technique and a tunable 785 nm laser to separate the fluorescence and the Raman spectrum from highly fluorescent samples, demonstrating the suitability of the probe for biomedical applications. Using this probe we also acquired fluorescence free human lung tissue data.
Photoacoustic microscopy (PAM) is a promising imaging modality because it is able to reveal optical absorption contrast in high resolution on the order of a micrometer. It can be applied in an endoscopic approach by implementing PAM into a miniature probe, termed as photoacoustic endoscopy (PAE). Here we develop a miniature focus-adjustable PAE (FA-PAE) probe characterized by both high resolution (in micrometers) and large depth of focus (DOF) via a novel optomechanical design for focus adjustment. To realize high resolution and large DOF in a miniature probe, a 2-mm plano-convex lens is specially adopted, and the mechanical translation of a single-mode fiber is meticulously designed to allow the use of multi-focus image fusion (MIF) for extended DOF. Compared with existing PAE probes, our FA-PAE probe achieves high resolution of 3-5 {mu}m within unprecedentedly large DOF of >3.2 mm, more than 27 times the DOF of the probe without performing focus adjustment for MIF. The superior performance is demonstrated by imaging both phantoms and animals including mice and zebrafishes in vivo. Our work opens new perspectives for PAE biomedical applications.
For the past forty years, optical fibres have found widespread use in ground-based and space-based instruments. In most applications, these fibres are used in conjunction with conventional optics to transport light. But photonics offers a huge range of optical manipulations beyond light transport that were rarely exploited before 2001. The fundamental obstacle to the broader use of photonics is the difficulty of achieving photonic action in a multimode fibre. The first step towards a general solution was the invention of the photonic lantern (Leon-Saval, Birks & Bland-Hawthorn 2005) and the delivery of high-efficiency devices (< 1 dB loss) five years on (Noordegraaf et al 2009). Multicore fibres (MCF), used in conjunction with lanterns, are now enabling an even bigger leap towards multimode photonics. Until recently, the single-moded cores in MCFs were not sufficiently uniform to achieve telecom (SMF-28) performance. Now that high-quality MCFs have been realized, we turn our attention to printing complex functions (e.g. Bragg gratings for OH suppression) into their N cores. Our first work in this direction used a Mach-Zehnder interferometer (near-field phase mask) but this approach was only adequate for N=7 MCFs as measured by the grating uniformity (Lindley et al 2014). We have now built a Sagnac interferometer that gives a three-fold increase in the depth of field sufficient to print across N > 127 cores. We achieved first light this year with our 500mW Sabre FRED laser. These are sophisticated and complex interferometers. We report on our progress to date and summarize our first-year goals which include multimode OH suppression fibres for the Anglo-Australian Telescope/PRAXIS instrument and the Discovery Channel Telescope/MOHSIS instrument under development at the University of Maryland.
We present the first label-free, non-contact, in-vivo imaging of the ocular vasculature using photoacoustic remote sensing (PARS) microscopy. Both anterior and posterior segments mouse eye were imaged. Vasculature of iris, sclera and retina tissues were clearly resolved. To best of our knowledge this the first study showing non-contact photoacoustic imaging conducted on in-vivo ocular tissue. We believe that PARS microscopy has the potential to advance the diagnosis and treatment of ocular diseases.
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