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Register a new userMiniature Probe for Optomechanical Focus-adjustable Optical-resolution Photoacoustic Endoscopy
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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.
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A photonic force microscope comprises of an optically trapped micro-probe and a position detection system to track the motion of the probe. Signal collection for motion detection is often carried out using the backscattered light off the probe - however, this mode has problems of low S/N due to the small back-scattering cross-sections of the micro-probes typically used. The position sensors often used in these cases are quadrant photodetectors. To ensure maximum sensitivity of such detectors, it would help if the detector size matched with the detection beam radius after the condenser lens (which for backscattered detection would be the trapping objective itself). To suit this condition, we have used a miniature displacement sensor whose dimensions makes it ideal to work with 1:1 images of micron-sized trapped probes in the back-scattering detection mode. The detector is based on the quadrant photo-IC in the optical pick-up head of a compact disc player. Using this detector, we measured absolute displacements of an optically trapped 1.1 um probe with a resolution of ~10 nm for a bandwidth of 10 Hz at 95% significance without any sample or laser stabilization. We characterized our optical trap for different sized probes by measuring the power spectrum for each probe to 1% accuracy, and found that for 1.1 um diameter probes, the noise in our position measurement matched the thermal resolution limit for averaging times up to 10 ms. We also achieved a linear response range of around 385 nm with crosstalk between axes ~4% for 1.1 um diameter probes. The detector has extremely high bandwidth (few MHz) and low optical power threshold - other factors that can lead to its widespread use in photonic force microscopy.
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.
Pump-probe experiments combining pulses from a X-ray FEL and an optical femtosecond laser are very attractive for sub-picosecond time-resolved studies. Since the synchronization between the two independent light sources to an accuracy of 100 fs is not yet solved, it is proposed to derive both femtosecond radiation pulses from the same electron bunch but from two insertion devices. This eliminates the need for synchronization and developing a tunable high power femtosecond quantum laser. In the proposed scheme a GW-level soft X-ray pulse is naturally synchronized with a GW-level optical pulse, independent of any jitter in the arrival time of the electron bunches. The concept is based on the generation of optical radiation in a master oscillator-power FEL amplifier (MOPA) configuration. X-ray radiation is generated in an X-ray undulator inserted between the modulator and radiator sections of the optical MOPA scheme. An attractive feature of the FEL amplifier scheme is the absence of any apparent limitations which could prevent operation in the femtosecond regime in a wide (200-900 nm) wavelength range. A commercially available long (nanosecond) pulse dye laser can be used as seed laser.
Although wireless capsule endoscopy is the preferred modality for diagnosis and assessment of small bowel diseases, the poor camera resolution is a substantial limitation for both subjective and automated diagnostics. Enhanced-resolution endoscopy has shown to improve adenoma detection rate for conventional endoscopy and is likely to do the same for capsule endoscopy. In this work, we propose and quantitatively validate a novel framework to learn a mapping from low-to-high resolution endoscopic images. We combine conditional adversarial networks with a spatial attention block to improve the resolution by up to factors of 8x, 10x, 12x, respectively. Quantitative and qualitative studies performed demonstrate the superiority of EndoL2H over state-of-the-art deep super-resolution methods DBPN, RCAN and SRGAN. MOS tests performed by 30 gastroenterologists qualitatively assess and confirm the clinical relevance of the approach. EndoL2H is generally applicable to any endoscopic capsule system and has the potential to improve diagnosis and better harness computational approaches for polyp detection and characterization. Our code and trained models are available at https://github.com/CapsuleEndoscope/EndoL2H.
We have developed a multimodal photoacoustic remote sensing (PARS) microscope combined with swept source optical coherence tomography for in vivo, non-contact retinal imaging. Building on the proven strength of multiwavelength PARS imaging, the system is applied for estimating retinal oxygen saturation in the rat retina. The capability of the technology is demonstrated by imaging both microanatomy and the microvasculature of the retina in vivo. To our knowledge this is the first time a non-contact photoacoustic imaging technique is employed for in vivo oxygen saturation measurement in the retina.
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