The flexible membranes used in MEMS tunable VCSELs are so small and light that thermally-induced vibrations can impact performance. We measure the thermal vibration spectrum of such a membrane showing peaks at the spatial vibration mode resonant frequencies of the membrane/plate. These vibrations result in a theoretical floor to the linewidth of the VCSEL. Frequency domain LiDAR and optical coherence tomography systems can get around this thermal linewidth limit with adequate clock measurement and processing. Essentially an OCT/LiDAR sweep with a concomitantly measured clock is a feed-forward linewidth reduction scheme. LiDAR ranging out to 10 meters has been demonstrated.
Optical coherence tomography (OCT) can be an important diagnostic tool in optics R&D and manufacturing. We illustrate this with four applications. (1) Imaging of vibration modes of MEMS membranes. (2) Strain mapping of VCSEL chips. (3) Optical frequency domain reflectometry (OFDR) of laser cavities. (4) Combined responsivity and 3D mapping of photodiode packages.
Side lobe artifacts on point spread functions can be traced back to (1) fringe visibility variation across the spectrum, (2) errors in sampling instances, and (3) window functions. We demonstrate signal processing methods for correcting for all three of these issues. These methods require a system calibration step. If the systems slowly age, the recalibration step could be performed in the field with a fixtured target.
Near infrared imaging methods, including optical coherence tomography (OCT), have shown promise in assessing activity of enamel caries lesions. We present initial results in ex-vivo dental samples with a polarization diversity-detection OCT system complete with an integrated dental handpiece. Built around an Axsun Technologies swept source engine, images B-scans 12(x) by 7(z) mm at over 100 fps with 66um transverse and 7um depth resolution. Internal normal dental structure and lesions were imaged and compared with micro-CT. We demonstrate that the Axsun OCT prototype can detect the penetration of occlusal lesions to dentin and measure the penetration of approximal lesions when imaging from the occlusal surface.
A 1060 nm optically pumped tunable VCSEL was formed from an InGaAs/AlGaAs/GaAs half-VCSEL bonded to a MEMS movable mirror on a silicon substrate. The VCSEL was co-packaged in a 14-pin butterfly module with an 825 nm pump laser and a 1060 nm semiconductor optical amplifier. The co-packaged device exhibited shot-noise-limited sensitivity with up to 50 mW output power and 75 nm tunability. Ophthalmic OCT, especially whole-eye imaging and ocular biometry, is considered the primary application of this device. However, we have also investigated LiDAR to greater than 10 meter ranges with non-mechanical beam steering through angular diffraction from a grating. A new generation of photonic integrated circuit LiDARs work this way and we have investigated the depth resolution limitations due to time dispersion from the grating. Distributed fiber temperature sensing was also demonstrated.
Endogenous fluorescence lifetime imaging (FLIM) provides direct access to the concomitant functional and biochemical changes accompanying tissue transition from benign to precancerous and cancerous. Since FLIM can noninvasively measure different and complementary biomarkers of precancer and cancer, we hypothesize that it will aid in clinically detecting early oral epithelial cancer. Our group has recently demonstrated the detection of benign from premalignant and malignant lesions based on endogenous multispectral FLIM in the hamster cheek-pouch model. Encouraged by these positive preliminary results, we have developed a handheld endoscope capable of acquiring multispectral FLIM images in real time from the oral mucosa. This novel FLIM endoscope is being used for imaging clinically suspicious pre-malignant and malignant lesions from patients before undergoing tissue biopsy for histopathological diagnosis of oral epithelial cancer. Our preliminary results thus far are already suggesting the potential of endogenous FLIM for distinguishing a variety of benign lesions from advanced dysplasia and squamous cell carcinoma (SCC). To the best of out knowledge, this is the first in vivo human study aiming to demonstrate the ability to predict the true malignancy of clinically suspicious lesions using endogenous FLIM. If successful, the resulting clinical tool will allow noninvasive real-time detection of epithelial precancerous and cancerous lesions in the oral mucosa and could potentially be used to assist at every step involved on the clinical management of oral cancer patients, from early screening and diagnosis, to treatment and monitoring of recurrence.
We present the use of a commercially available electrically tunable lens to achieve axial scanning in a reflectance confocal microscope. Over a 255 μm axial scan range, the lateral and axial resolutions varied from 1-2 μm and 4-14 μm, respectively, dependent on the variable focal length of the tunable lens. Confocal imaging was performed on normal human biopsies from the oral cavity ex vivo. Sub-cellular morphologic features were seen throughout the depth of the epithelium while axially scanning using the focus tunable lens.
Optical imaging techniques using a variety of contrast mechanisms are under evaluation for early detection of epithelial precancer; however, tradeoffs in field of view (FOV) and resolution may limit their application. Therefore, we present a multiscale multimodal optical imaging system combining macroscopic biochemical imaging of fluorescence lifetime imaging (FLIM) with subcellular morphologic imaging of reflectance confocal microscopy (RCM). The FLIM module images a 16×16 mm2 tissue area with 62.5 μm lateral and 320 ps temporal resolution to guide cellular imaging of suspicious regions. Subsequently, coregistered RCM images are acquired at 7 Hz with 400 μm diameter FOV, <1 μm lateral and 3.5 μm axial resolution. FLIM-RCM imaging was performed on a tissue phantom, normal porcine buccal mucosa, and a hamster cheek pouch model of oral carcinogenesis. While FLIM is sensitive to biochemical and macroscopic architectural changes in tissue, RCM provides images of cell nuclear morphology, all key indicators of precancer progression.
Current methods for detection of oral cancer lack the ability to delineate between normal and precancerous tissue
with adequate sensitivity and specificity. The usual diagnostic mechanism involves visual inspection and palpation
followed by tissue biopsy and histopathology, a process both invasive and time-intensive. A more sensitive and
objective screening method can greatly facilitate the overall process of detection of early cancer. To this end, we
present a multimodal imaging system with fluorescence lifetime imaging (FLIM) for wide field of view guidance
and reflectance confocal microscopy for sub-cellular resolution imaging of epithelial tissue. Moving from a 12 x 12
mm2 field of view with 157 ìm lateral resolution using FLIM to 275 x 200 μm2 with lateral resolution of 2.2 μm using confocal microscopy, hamster cheek pouch model is imaged both in vivo and ex vivo. The results indicate that
our dual modality imaging system can identify and distinguish between different tissue features, and, therefore, can
potentially serve as a guide in early oral cancer detection..
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