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Diffuse optical tomography (DOT) is a noninvasive imaging technique in which near-infrared light is used to probe the interior of the body for oxygenation and other physiological changes. Applications include brain monitoring, optical mammography, and diagnostic imaging of joints and limbs.
A major challenge in optical imaging of biological tissue is the strong scattering of visible and infrared light by tissue. Unlike x-rays, low-energy photons do not travel through the body in a straight line, but instead propagate in a diffuse manner and thus carry little spatial information about the volume. DOT systems deal with this situation by using an array of detectors to sample as much reflected light as possible over a surface area, and then processing this information with statistical models of photon transport to generate cross-sectional or 3-D images of the tissue. In addition to structural data, these images provide functional information about the tissue, which can be derived from the typical absorption spectra of specific molecular species such as oxy- and deoxyhemoglobin.
DOT systems use various types of measurement methods, including frequency domain measurement, continuous wave measurement, and time-resolved methods such as time-correlated photon counting. Measurements are mostly made at wavelengths between 750 nm and 1000 nm. Typically, detectors placed close to the light source will detect light scattered from tissue just below the surface, while detectors placed further away will detect light from deeper tissue where the signal is very weak. Imaging deeper tissue thus requires detectors with high sensitivity and wide dynamic range. Detectors should also have excellent time or frequency response in order to discriminate between surface scattering and deep-tissue scattering.
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