Interferometers for optical coherence domain reflectometry...

Optics: measuring and testing – By light interference

Reexamination Certificate

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Reexamination Certificate

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06657727

ABSTRACT:

BACKGROUND OF THE INVENTION
Optical Coherence Tomography (OCT) is a novel imaging technique which allows for noninvasive cross-sectional imaging in scattering or cloudy media with high spatial resolution and high dynamic range. OCT is a two-dimensional extension of Optical Coherence-Domain Reflectometry (OCDR) which is also commonly referred to as Optical Low Coherence Reflectometry (OLCR), in which a low temporal coherence light source is employed to obtain precise localization of reflections internal to a probed structure along the optic axis. The one-dimensional ranging technique of OCDR/OLCR has previously been utilized for characterization of bulk-, integrated-, and fiber-optic structures, as well as biological tissues. In OCT, this technique is extended to provide for scanning of the probe beam in a direction perpendicular to the optic axis, building up a two-dimensional data set comprising a cross-sectional image of internal tissue backscatter.
Ophthalmic Applications of OCT
OCT has previously been applied to imaging of biological tissues in vivo and in vitro, although the majority of initial biomedical imaging studies concentrated on transparent structures such as the eye. Initial ophthalimic imaging studies demonstrated significant potential for OCT imaging in routine examination of normal and abnormal ocular structures, including imaging of the cornea, iris, and other structures of the anterior eye; the lens and lens capsule; and numerous structures in the posterior eye, including the neurosensory retina, retinal nerve fiber layer, retinal pigment epithelium, and choroid. In OCT examination of the retina, initial in vivo clinical studies have demonstrated its utility in aiding diagnosis in a variety of vitreoretinal diseases, including macular hole, macular degeneration, detached retina, and glaucoma. Clinical trials of OCT imaging for ophthalmic applications are currently under way at several centers, and a commercial ophthalmic OCT scanner is available from Humphrey Systems of Dublin, Calif.
OCT Imaging in Highly Scattering Media
Several recent publications have demonstrated the potential applications of OCT in highly scattering media for the measurement of tissue optical properties and imaging. Optical imaging in scattering media such as biological tissue is in general a very difficult problem, particularly for techniques such as OCT which depend primarily upon unscattered or singly-scattered light for image formation. It has been observed in preliminary studies and theoretical treatments that this singly-scattered gating requirement practically limits OCT imaging to a useful penetration depth of a few millimeters at best in nontransparent human tissues. Nonetheless, several authors have identified diagnostic scenarios in which a technique for improved, non-invasive 10-20-micron scale optical imaging near tissue surfaces has significant potential for clinical utility. These include applications of OCT imaging in skin, teeth, vascular tissues, and gastrointestinal mucosa. The latter two examples are significant since with its fiber optic implementation, OCT is readily adaptable to minimally invasive diagnostic modalities such as catheterization or endoscopy. OCT system implementations featuring the high-speed imaging acquisition necessary for in vivo application and catheter/endoscopic delivery have been reported. The application of OCT to biomedical imaging provides the potential for sub-surface tissue characterization with sufficient resolution to provide microscopic morphological information relevant to pathological diagnosis without the need for biopsy.
OCT Imaging in Industrial Processing
Recent publications have also illustrated the potential applications of OCT for imaging in cloudy or turbid non-biological media in industrial processing in the manufacturing industry. OCT imaging may be useful for on-line process control or product testing and evaluation. Initial experiments have demonstrated OCT imaging in ceramic and other highly scattering materials, as well as for the characterization of the surface topology of opaque industrial materials such as metals (i.e., ball bearings).
OCT Oualitative Technical Description
Optical coherence tomography performs micron-scale topographic imaging of internal tissue microstructure using a combination of the principles of low-coherence interferometry and confocal microscopy. Reference is made to
FIG. 1
illustrating an exemplary OCT system
10
in which the tissue to be examined is placed in the sample arm
12
of a Michelson interferometer illuminated by a broadband light source
16
. Due to the limited coherence length of the source (typically 10-15 microns), light returning from the reference arm
18
and light backscattered by internal sample reflections interferes constructively or destructively only when the interferometer arm optical path lengths are matched to within the source coherence length. Scanning the reference arm
18
length through a position corresponding to the depth of a reflecting site within the sample generates a localized interference pattern, which is recorded as a localized modulation of the detector current as a function of the reference arm position. A beamsplitter
20
, optical detector
22
, transimpedance amplifier
24
, demodulator
26
, AID converter
28
, and display
30
are also shown. The detector current generated by a sample containing multiple reflecting sites distributed along its depth (such as biological tissue) contains the sum of multiple, overlapping copies of this interference pattern. A map of tissue reflectivity versus depth or “A-Scan” is obtained by scanning the reference mirror
32
at constant velocity, while recording the envelope of the detector current. The envelope may be recorded with high dynamic range by scanning the reference mirror
32
at fixed velocity, and demodulating the detector current at the resulting Doppler frequency. Cross-sectional images of tissue backscatter or “B-Scans” may be acquired by obtaining sequential A-scans while scanning the probe beam across the tissue surface using a lateral beam scanning mirror
33
or some other lateral scanning optic device. The resulting two-dimensional datasets are plotted as gray-scale or false-color images.
A significant advantage of using low-coherence interferometry for signal detection is that the interferometer
14
acts as an optical heterodyne detector, providing a dramatic expansion in dynamic range compared to direct detection of scattered light. Since the interferometric component of the detector current is proportional to the product of the electric field amplitudes returning from each arm, the detected envelope signal is proportional to the square root of the sample power reflectivity. Extremely faint reflections in the sample (~10
−11
times the incident optical power) are routinely detected in A-scans recorded in a fraction of a second. As illustrated in
FIG. 1
, the interferometer
14
can also be implemented using inexpensive semiconductor sources and detectors, and flexible single-mode optical fibers suitable for remote imaging through minimally invasive diagnostic instruments.
Signal-To-Noise Ratio in OCDR and OCT
A significant limitation in the use of OCDR and OCT in highly scattering media is that the OCT probe light is very strongly (exponentially) attenuated in the scattering material, thus limiting the imaging depth which can be achieved in a given amount of time for a given sensitivity. For a conventional OCT system in which a 50/50 beamsplitter
20
is used in the Michelson interferometer, the signal to noise ratio (SNR) of the detected electronic signal in the shot-noise limit is given by Eq. (1) below:
SNR
=
ρ



P
s

R
s
2



qB
(
1
)
In this expression, SNR is signal-to-noise ratio (a measure of the sensitivity which also relates to imaging depth in scattering media), &rgr; is the detector responsivity, P
s
is the optical power incident on the sample, R
s
is the optical power reflectivity of the sample, q is the charge on the electr

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