Optical coherence tomography (OCT) is an interferometric, non-invasive optical tomographic imaging technique offering millimeter penetration (approximately 2--3 mm in tissue) with sub-micrometre axial and lateral resolution. The technique was first demonstrated in 1991 with ~30µm axial resolution. Since then, OCT has achieved sub-micrometre resolution in 2001 due to introduction of wide bandwidth light sources (sources emitting wavelengths over a ~100 nm range). By now OCT has found its place as a widely accepted imaging technique, especially in ophthalmology and other biomedical applications.
With micrometer resolution and cross-sectional imaging capabilities, optical coherence tomography (OCT)1 has become a prominent biomedical tissue imaging technique; it is particularly suited to ophthalmic applications and in other tissue imaging requiring micrometer resolution and millimeter penetration depth. OCT has critical advantages over other medical imaging systems. Medical ultrasonography, magnetic resonance imaging (MRI) and confocal microscopy are not suited to morphological tissue imaging; the former two having poor resolution; the latter lacking millimeter penetration depth2,3.
OCT works through the magic of low-coherence interferometry4,5,6. In conventional interferometry with long coherence length (laser interferometry), interference of light occurs over a distance of meters. In OCT, this interference is shortened to a distance of micrometres, thanks to the use of broadband light sources (sources that can emit light over a broad range of frequencies). Light with broad bandwidths can be generated by using superluminescent diodes (superbright LED's) or lasers with extremely short pulses (femtosecond lasers). White light is also a broadband source with lower powers.
Light in an OCT system is broken into two arms -- a sample arm (containing the item of interest) and a reference arm (usually a mirror). The combination of backscattered light from the sample arm and reference light from the reference arm gives rise to an interference pattern, but only if light from both arms have travelled the "same" optical distance ("same" meaning a difference of less than a coherence length). By scanning the mirror in the reference arm, a reflectivity profile of the sample can be obtained (this is time domain OCT). Areas of the sample that reflect back a lot of light will create greater interference than areas that don't. Any light that is outside the short coherence length will not interfere. This reflectivity profile, called an A-scan contains information about the spatial dimensions and location of structures within the item of interest. A cross-sectional tomograph (B-scan) may be achieved by laterally combining a series of these axial depth scans (A-scan). En face imaging (C-scan) at an acquired depth is possible depending on the imaging engine used.
The principle OCT is white light or low coherence interferometry. The optical setup typically consists of an interferometer (Fig. 1, typically Michelson type) with a low coherence, broad bandwidth light source. Light is split into and recombined from reference and sample arm, respectively.
The interference of two partially coherent light beams can be expressed in terms of the source intensity, , as
where represents the interferometer beam splitting ratio, and is called the complex degree of coherence, i.e. the interference envelope and carrier dependent on reference arm scan or time delay , and whose recovery of interest in OCT. Due to the coherence gating effect of OCT the complex degree of coherence is represented as a Gaussian function expressed as6
where represents the spectral width of the source in the optical frequency domain, and is the centre optical frequency of the source. In equation (2), the Gaussian envelope is amplitude modulated by an optical carrier. The peak of this envelope represents the location of sample under test microstructure, with an amplitude dependent on the reflectivity of the surface. The optical carrier is due to the Doppler effect resulting from scanning one arm of the interferometer, and the frequency of this modulation is controlled by the speed of scanning. Therefore translating one arm of the interferometer has two functions; depth scanning and a Doppler-shifted optical carrier are accomplished by pathlength variation. In OCT, the Doppler-shifted optical carrier has a frequency expressed as
where is the central optical frequency of the source, is the scanning velocity of the pathlength variation, and is the speed of light.
The axial and lateral resolutions of OCT are decoupled from one another; the former being an equivalent to the coherence length of the light source and the latter being a function of the optics. The coherence length of a source and hence the axial resolution of OCT is defined as
Focusing the light beam to a point on the surface of the sample under test, and recombining the reflected light with the reference will yield an interferogram with sample information corresponding to a single A-scan (Z axis only). Scanning of the sample can be accomplished by either scanning the light on the sample, or by moving the sample under test. A linear scan will yield a two-dimensional data set corresponding to a cross-sectional image (X-Z axes scan), whereas an area scan achieves a three-dimensional data set corresponding to a volumetric image (X-Y-Z axes scan), also called full-field OCT.
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Optische Kohärenztomographie | Tomografia ottica a coerenza di fase
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