No Arabic abstract
Optical coherence tomography (OCT) is a powerful biomedical imaging technology that relies on the coherent detection of backscattered light to image tissue morphology in vivo. As a consequence, OCT is susceptible to coherent noise (speckle noise), which imposes significant limitations on its diagnostic capabilities. Here we show a method based purely on light manipulation that is able to entirely remove the speckle noise originating from turbid samples without any compromise in resolution. We refer to this method as Speckle-Free OCT (SFOCT). Using SFOCT, we succeeded in revealing small structures that are otherwise hidden by speckle noise when using conventional OCT, including the inner stromal structure of a live mouse cornea, the fine structures inside the mouse pinna, sweat ducts, and Meissners corpuscle in the human fingertip skin. SFOCT has the potential to markedly increase OCTs diagnostic capabilities of various human diseases by revealing minute features that correlate with early pathology.
We demonstrate an ultrahigh-speed optical coherence tomography (OCT) based on a 100 MHz swept source (SS). An all polarization-maintaining figure-9 mode-locked fiber laser is used as the seed laser. After nonlinear spectral expansion in an Erbium-doped fiber amplifier, a flat top spectrum with respectively 1-dB and 10-dB bandwidths of 73.7 nm and 106 nm is obtained. The broadband femtosecond pulse is time stretched to a swept signal in a section of dispersion compensation fiber with a total dispersion of -84 ps/nm. With the swept source, the axial resolution of the SS-OCT is measured to be 21 um with a 6 dB sensitivity roll-off length of 3 mm. A tomographic image of an encoding disk and a hard disk jointly rotating at 17,000 rpm was acquired by using the SS-OCT with a high imaging quality.
We report on the use of radio-frequency optical atomic magnetometers for magnetic induction tomography measurements. We demonstrate the imaging of dummy targets of varying conductivities placed in the proximity of the sensor, in an unshielded environment at room-temperature and without background subtraction. The images produced by the system accurately reproduce the characteristics of the actual objects. Furthermore, we perform finite element simulations in order to assess the potential for measuring low-conductivity biological tissues with our system. Our results demonstrate the feasibility of an instrument based on optical atomic magnetometers for magnetic induction tomography imaging of biological samples, in particular for mapping anomalous conductivity in the heart.
Laser speckle can provide a powerful tool that may be used for metrology, for example measurements of the incident laser wavelength with a resolution beyond that which may be achieved in a commercial device. However, to realise highest resolution requires advanced multi-variate analysis techniques, which limit the acquisition rate of such a wavemeter. Here we show an arithmetically simple method to measure wavelength changes with dynamic speckle, based on a Poincar`e descriptor of the speckle pattern. We demonstrate the measurement of wavelength changes at femtometer-level with a measurement time reduced by two orders of magnitude compared to the previous state-of-the-art, which offers promise for applications such as speckle-based laser wavelength stabilisation.
Noninvasive optical imaging through dynamic scattering media has numerous important biomedical applications but still remains a challenging task. While standard methods aim to form images based upon optical absorption or fluorescent emission, it is also well-established that the temporal correlation of scattered coherent light diffuses through tissue much like optical intensity. Few works to date, however, have aimed to experimentally measure and process such data to demonstrate deep-tissue imaging of decorrelation dynamics. In this work, we take advantage of a single-photon avalanche diode (SPAD) array camera, with over one thousand detectors, to simultaneously detect speckle fluctuations at the single-photon level from 12 different phantom tissue surface locations delivered via a customized fiber bundle array. We then apply a deep neural network to convert the acquired single-photon measurements into video of scattering dynamics beneath rapidly decorrelating liquid tissue phantoms. We demonstrate the ability to record video of dynamic events occurring 5-8 mm beneath a decorrelating tissue phantom with mm-scale resolution and at a 2.5-10 Hz frame rate.
Many areas of optical science require an accurate measurement of optical spectra. Devices based on laser speckle promise compact wavelength measurement, with attometer-level sensitivity demonstrated for single wavelength laser fields. The measurement of multimode spectra using this approach would be attractive, yet this is currently limited to picometer resolution. Here, we present a method to improve the resolution and precision of speckle-based multi-wavelength measurements. We measure multiple wavelengths simultaneously, in a device comprising a single 1 m-long step-index multimode fiber and a fast camera. Independent wavelengths separated by as little as 1 fm are retrieved with 0.2 fm precision using Principal Component Analysis. The method offers a viable way to measure sparse spectra containing multiple individual lines and is likely to find application in the tracking of multiple lasers in fields such as portable quantum technologies and optical telecommunications.