Three-dimensional ultrahigh resolution optical coherence tomography of macular pathologies

purpose. To demonstrate a new generation of three-dimensional (3-D) ultrahigh-resolution optical coherence tomography (UHR OCT) technology for visualization of macular diseases. methods. One hundred forty eyes with a distinct disease in each of the posterior pole compartments were examined with 3-D UHR OCT. 3-D imaging was performed with a high axial resolution of 3 ?m with a compact, commercially available, ultra–broad-bandwidth (160 nm) titanium:sapphire laser at a video rate of up to 25 B-scans/s. Each tomogram consisted of 1024 × 1024 pixels, resulting in 25 megavoxels/s. results. 3-D UHR OCT offers high-precision 3-D visualization of macular diseases at all structural levels. The UHR modality allows identification of the contour of the hyaloid membrane, tractive forces of epiretinal membranes, and changes within the inner limiting membrane. The system provides quality 3-D images of the topographic dynamics of traction lines from the retinal surface down to the level of the photoreceptor segments. Intraretinal diseases are identified by their specific location in different layers of the neurosensory ultrastructure. Photoreceptor inner and outer segments are clearly delineated in configuration and size, with a characteristic peak in the subfoveal area. The microarchitecture of choroidal neovascularization is distinctly imaged, related leakage can be identified, and the volume can be quantified. conclusions. High-speed UHR OCT offers unprecedented, realistic, 3-D imaging of ocular diseases at all epi-, intra- and subretinal levels. A complete 3-D data set of the macular layers allows a comprehensive analysis of focal and diffuse diseases, as well as identification of dynamic pathomechanisms

Full-field time-encoded frequency-domain optical coherence tomography

Ultrahigh axial resolution surface profiling as well as volumetric optical imaging based on time encoded optical coherence tomography in the frequency domain without any mechanical scanning element is presented. A frequency tuned broad bandwidth titanium sapphire laser is interfaced to an optical microscope (Axioskop 2 MAT, Carl Zeiss Meditec) that is enhanced with an interferometric imaging head. The system is equipped with a 640 x 480 pixel CMOS camera, optimized for the 800 nm wavelength tuning range for transmission and reflection measurements of a microscopic sample. Sample volume information over 1.3 x 1 x 0.2 m

First report of the parasitic copepod

Lernaea cyprinacea is a non host-specific parasitic copepod known to infest many freshwater fish species. Outbreaks of infestations by this ectoparasite may cause mass mortality of parasitized fishes. L. cyprinacea has been found mostly on pelagic species. Records on small benthic fish species are less common. Especially rare are infestations of Gobioidei adapted to a benthic life style, with reports restricted to Asia and, in Europe, to the Ponto-Caspian region. Although it is cosmopolitan, L. cyprinacea has rarely been found in Italy. One of the few Italian localities with documented infestations is Lake Trasimeno, a lake with an economically important fishery. Although endoparasites of commercially interesting fish species in this lake are well documented, information about ectoparasites is rare. In May 2015, specimens of two gobioids − Knipowitschia panizzae and Pomatoschistus canestrinii − infested with L. cyprinacea were sampled at the south shore of Lake Trasimeno. Both gobies are not native to the lake. This is the first documentation of gobioid fishes as hosts of L. cyprinacea in Italy and in Europe (outside of the Ponto-Caspian region). Although both gobies are not optimal hosts (small size, short life expectancy) they have the potential to carry and to transmit the parasite in freshwater habitats, e.g. by unintentional introduction with fry of other fish species

First report of the parasitic copepod Lernaea cyprinacea (Copepoda: Lernaeidae) on gobioid fishes (Teleostei: Gobonellidae) in southern Europe

Lernaea cyprinacea is a non host-specific parasitic copepod known to infest many freshwater fish species. Outbreaks of infestations by this ectoparasite may cause mass mortality of parasitized fishes. L. cyprinacea has been found mostly on pelagic species. Records on small benthic fish species are less common. Especially rare are infestations of Gobioidei adapted to a benthic life style, with reports restricted to Asia and, in Europe, to the Ponto-Caspian region. Although it is cosmopolitan, L. cyprinacea has rarely been found in Italy. One of the few Italian localities with documented infestations is Lake Trasimeno, a lake with an economically important fishery. Although endoparasites of commercially interesting fish species in this lake are well documented, information about ectoparasites is rare. In May 2015, specimens of two gobioids − Knipowitschia panizzae and Pomatoschistus canestrinii − infested with L. cyprinacea were sampled at the south shore of Lake Trasimeno. Both gobies are not native to the lake. This is the first documentation of gobioid fishes as hosts of L. cyprinacea in Italy and in Europe (outside of the Ponto-Caspian region). Although both gobies are not optimal hosts (small size, short life expectancy) they have the potential to carry and to transmit the parasite in freshwater habitats, e.g. by unintentional introduction with fry of other fish species

Polarization sensitive optical coherence tomography of melanin provides tissue inherent contrast based on depolarization

Polarization sensitive optical coherence tomography (PS-OCT) was used to investigate the polarization properties of melanin. Measurements in samples with varying melanin concentrations revealed polarization scrambling, i.e. depolarization. The results indicate that the depolarizing appearance of pigmented structures like, for instance, the retinal pigment epithelium (RPE) is likely to be caused by the melanin granules contained in these cells.Austrian Science Fund (FWF grants P19624-B02 and P19751-N20

Ultrahigh resolution optical coherence tomography of the monkey fovea. Identification of retinal sublayers by correlation with semithin histology sections

Optical coherence tomography (OCT) has become an established diagnostic tool for the clinical assessment of retinal pathology but correlation of acquired signals with retinal substructures has often been ambiguous. In the monkey retina we have now obtained ultrahigh resolution (UHR) OCT images with 1·4 μm axial×3 μm transverse resolution from perfusion-fixed eye cups of Macaca fascicularis and optimized the identification of retinal anatomy by correction of spatial artefacts in correlated histology. After resin embedding, serial semithin sections were obtained that corresponded to OCT transects. The direct overlay of features identified in histological sections with corresponding OCT locations was limited by non-linear tissue shrinkage due to dehydration and sectioning stress. In the present study, these misalignments were further corrected by using polygonal spline morphing based on corresponding unequivocal landmarks. The geometric normalization then allowed detailed comparison of both profiles including delicate sublayers of photoreceptor inner- and outer segments. Such correlation will facilitate the extraction of structural information from in vivo ultrahigh resolution OCT images in clinical and experimental applications

Three-dimensional adaptive optics ultrahigh-resolution optical coherence tomography using a liquid crystal spatial light modulator

AbstractA liquid crystal programmable phase modulator (PPM) is used as correcting device in an adaptive optics system for three-dimensional ultrahigh-resolution optical coherence tomography (UHR OCT). The feasibility of the PPM to correct high order aberrations even when using polychromatic light is studied, showing potential for future clinical use. Volumetric UHR OCT of the living retina, obtained with up 25,000A-scans/s and high resolution enables visualization of retinal features that might correspond to groups of terminal bars of photoreceptors at the external limiting membrane

Enhanced visualization of macular pathology with the use of ultrahigh resolution optical coherence tomography

Objectives To demonstrate a new generation of ophthalmic optical coherence tomography (OCT) technology with unprecedented axial resolution for enhanced imaging of intraretinal microstructures and to investigate its clinical feasibility to visualize intraretinal morphology of macular pathology. Methods A clinically viable ultrahigh-resolution ophthalmic OCT system was developed and used in clinical imaging for the first time. Fifty-six eyes of 40 selected patients with different macular diseases including macular hole, macular edema, age-related macular degeneration, central serous chorioretinopathy, epiretinal membranes, and detachment of pigment epithelium and sensory retina were included. Outcome Measures Ultrahigh-resolution tomograms visualizing intraretinal morphologic features in different retinal diseases. Results An axial image resolution of approximately

Imaging ex vivo and in vitro brain morphology in animal models with ultrahigh resolution optical coherence tomography

The feasibility of ultrahigh resolution optical coherence tomography (UHR OCT) to image ex vivo and in vitro brain tissue morphology on a scale from single neuron cells to a whole animal brain was investigated using a number of animal models. Sub-2-microm axial resolution OCT in biological tissue was achieved at different central wavelengths by separately interfacing two state-of-the-art broad bandwidth light sources (titanium:sapphire, Ti:Al2O3 laser, lambdac=800 nm, Deltalambda=260 nm, Pout=50 mW and a fiber laser light source, lambdac=1350 nm, Deltalambda=470 nm, Pout=4 mW) to free-space or fiber-based OCT systems, designed for optimal performance in the appropriate wavelength regions. The ability of sub-2-microm axial resolution OCT to visualize intracellular morphology was demonstrated by imaging living ganglion cells in cultures. The feasibility of UHR OCT to image the globular structure of an entire animal brain as well as to resolve fine morphological features at various depths in it was tested by imaging a fixed honeybee brain. Possible degradation of OCT axial resolution with depth in optically dense brain tissue was examined by depositing microspheres through the blood stream to various depths in the brain of a living rabbit. It was determined that in the 1100 to 1600-nm wavelength range, OCT axial resolution was well preserved, even at depths greater than 500 microm, and permitted distinct visualization of microspheres 15 microm in diameter. In addition, the OCT image penetration depth and the scattering properties of gray and white brain matter were evaluated in tissue samples from the visual cortex of a fixed monkey brain

Visualization 1: Phase-stable swept source OCT angiography in human skin using an akinetic source

Visulization 1 Originally published in Biomedical Optics Express on 01 August 2016 (boe-7-8-3032