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Changes in the pattern and distribution of both melanocytes (pigment producing) and vasculature (hemoglobin containing) are important in distinguishing melanocytic proliferations. The ability to accurately measure melanin distribution at different depths and to distinguish it from hemoglobin is clearly important when assessing pigmented lesions (benign versus malignant). We have developed a multimode hyperspectral dermoscope (SkinSpect™) able to more accurately image both melanin and hemoglobin distribution in skin. SkinSpect uses both hyperspectral and polarization-sensitive measurements. SkinSpect’s higher accuracy has been obtained by correcting for the effect of melanin absorption on hemoglobin absorption in measurements of melanocytic nevi. In vivo human skin pigmented nevi (N=20) were evaluated with the SkinSpect, and measured melanin and hemoglobin concentrations were compared with spatial frequency domain spectroscopy (SFDS) measurements. We confirm that both systems show low correlation of hemoglobin concentrations with regions containing different melanin concentrations (R=0.13 for SFDS, R=0.07 for SkinSpect).

We have developed a multimode dermoscope (SkinSpect™) capable of illuminating human skin samples in-vivo with spectrally-programmable linearly-polarized light at 33 wavelengths between 468nm and 857 nm. Diffusely reflected photons are separated into collinear and cross-polarized image paths and images captured for each illumination wavelength. In vivo human skin nevi (N = 20) were evaluated with the multimode dermoscope and melanin and hemoglobin concentrations were compared with Spatially Modulated Quantitative Spectroscopy (SMoQS) measurements. Both systems show low correlation between their melanin and hemoglobin concentrations, demonstrating the ability of the SkinSpectTM to separate these molecular signatures and thus act as a biologically plausible device capable of early onset melanoma detection.

A polarization-sensitive hyperspectral imaging system (SkinSpect) has been built and evaluated using two-layer tissue phantoms, fabricated to mimic the optical properties of melanin in different epidermal thickness and hemoglobin in dermal layers. Multiple tissue-mimicking phantoms with varying top layer thicknesses were measured for optical system calibration and performance testing. Phantom properties were characterized and validated using SkinSpect. The resulting analysis shows that the proposed system is capable of distinguishing and differentiating the layer-dependent absorption spectra and the depths at which this absorption occurs.

We present a polarization-sensitive hyperspectral imaging system (SkinSpect) that employs a spectrally-programmable light source in the visible and NIR domains. Multiple tissue-mimicking phantoms were fabricated to mimic the optical properties of normal skin as well as pigmented light and dark moles. The phantoms consist of titanium dioxide and a mixture of coffee, red food dye, and naphthol green as the scattering and the three absorptive agents in a polydimethylsiloxane (PDMS) base. Phantoms were produced with both smooth and rough textured surfaces and tested using Spatial Frequency Domain Imaging (SFDI) and Spatially Modulated Quantitative Spectroscopy (SMoQS) for homogeneity as well as determining absorption and scattering variance, respectively. The reflectance spectral images were also recorded using the SkinSpect research prototype; the spectral signatures of the phantoms were calculated using a two-flux single-layer Kubelka-Munk model and non-negative least square fitting routine was applied to extract the relative concentrations of the individual phantom components. © 2013 Copyright SPIE.

When imaging through turbid media, objects are often blurred by scattered light. An optical collimator (i.e., an angular filter array) improves images by accepting only photons propagating within a narrow solid angle about the direction of the incident light. These photons are expected to participate in a limited number of small-angle scattering events, maintaining their original propagation direction and, finally, contributing to the development of a faithful image of an object within a turbid medium. The collimation method, also referred to as angular domain imaging (ADI), applies to a see-through configuration where the incident collimated light beam can be aligned with the collimator in a transillumination mode of operation. In this paper, we present angular domain optical projection tomography (ADOPT), a method that can extract depth information of optical contrast in turbid media with high longitudinal resolution based on ADI technology. The resolution of the ADI system has been tested over various depths in a 5 cm optical cuvette using a resolution target suspended in a homogeneous turbid medium. The ADOPT system reconstructed images from a series of angular domain projections collected at angular intervals. The system was used to measure the attenuation of an absorbing target in transmission mode (t-ADOPT) and to measure the light emitting from a fluorescent target (f-ADOPT). Tissue-mimicking phantoms were used to validate the performance of the method. In the t-ADOPT configuration, a background scattered light estimation and subtraction methodology was introduced to improve the imaging contrast. A target consisting of two graphite rods (0.9 mm diameter) was suspended in the cuvette by a rotation stage. An Indocyanine Green-filled glass rod was used as an imaging target in the f-ADOPT arrangement. The target was placed in a manner such that the line of laser light was perpendicular to the longitudinal axis of the rods. Several projections were collected at increments of 1.8[degrees] and compiled into a sinogram. A transverse image was reconstructed from the sinogram by using filtered backprojection and image contrast was improved by experimental scatter measurements using a wedge prism and an image processing algorithm. The submillimeter target embedded in a 2 cm thick scattering medium (reduced scattering coefficient [is less than or equal to] 2.4 [cm.sup.-1]) was discernable in both the sinograms and the reconstructed images. In the f-ADOPT system, fluorescent line targets < 1 cm in diameter embedded in a 2 cm thick scattering medium (reduced scattering coefficient [is less than or equal to] 0.8 [cm.sup.-1]) were discernable in both the sinograms and the reconstructed images. The proposed method could be used as the basis to construct an optical tomographic scanner for simultaneous absorption and fluorescence-based imaging of biological specimens (i.e., up to 7mm across). OCIS codes: 110.0113, 120.1680, 120.5820.