USRE41949E1 - System and method for tomographic imaging of dynamic properties of a scattering medium - Google Patents

System and method for tomographic imaging of dynamic properties of a scattering medium Download PDF

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USRE41949E1
USRE41949E1 US11/525,188 US52518800D USRE41949E US RE41949 E1 USRE41949 E1 US RE41949E1 US 52518800 D US52518800 D US 52518800D US RE41949 E USRE41949 E US RE41949E
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energy
fiber bundles
source
detectors
scattering medium
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Randall L. Barbour
Christoph H. Schmitz
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Research Foundation of State University of New York
US Department of Health and Human Services
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    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
    • G01N21/17—Systems in which incident light is modified in accordance with the properties of the material investigated
    • G01N21/47—Scattering, i.e. diffuse reflection
    • G01N21/4795—Scattering, i.e. diffuse reflection spatially resolved investigating of object in scattering medium

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  • the invention relates to a system and method for tomographic imaging of dynamic properties of a scattering medium, which may have special application to medical imaging, and in particular to systems and methods for tomographic imaging using near infrared energy to image time variations in the optical properties of tissue.
  • NIR-imaging methods Contrary to imaging methods relying on the use of ionizing radiation and/or toxic/radioactive contrast agents, near infra-red (NIR)-imaging methods bear no known risk of causing harm to the patient.
  • the dose of optical intensity used remains far below the threshold of thermal damage and is therefore safe.
  • wavelength/intensity/power used there are no effects on patient tissue that accumulate with increasing NIR dose due to over-all irradiation time.
  • optical tomography especially gains from the development of small, economical, yet powerful semiconductor lasers (laser diodes) and the availability of highly integrated, economical off-the-shelf data processing electronics suitable for the application. Moreover, the availability of powerful yet inexpensive computers contributes to the attractiveness of optical tomography since a significant computational effort may be necessary for both image reconstruction and data analysis.
  • Optical tomography yields insights into anatomy and physiology that are unavailable from other imaging methods, since the underlying biochemical activities of physiological processes almost always leads to changes in tissue optical properties. For example, imaging blood content and oxygenation is of interest. Blood shows prominent absorption spectra in the NIR region and vascular dynamics and blood oxygenation play a major role in physiology/pathology.
  • the present invention provides a system and method for generating an image of dynamic properties in a scattering medium.
  • the system includes an energy source, such as a NIR emitting source, and a detection system to measure received energy.
  • the detection system has at least one photo-detector such as a photodiode, a means for rapid adjustment of signal gain, and a device for retaining a measured response in order to investigate the dynamic variations in the optical properties of tissues.
  • the detection system further may also include at least one means for separating a plurality of signals from the photo-receiver when multiple energy sources are used simultaneously. This simultaneous use of multiple energy sources allows the use of different wavelengths and/or different source locations at the same time.
  • a specimen is exposed to NIR light emitted from at least one laser diode.
  • an imaging head may be utilized that contains means for positioning at least one source location and / or at least one detector location with respect to the medium.
  • the energy detector may use an energy collecting element, such as an optical fiber to transmit the received energy.
  • the energy detector is responsive to the energy or light emerging from the specimen.
  • the signal from the detector is selectively enhanced in gain to increase the dynamic measurement range.
  • the method may further include separating via at least one lock-in amplifier a plurality of signals generated by multiple energy sources.
  • the method allows simultaneous measurements of signals produced by the NIR light by means of a sample-and-hold circuit when more than one detector fiber is used.
  • FIG. 1 is a block diagram of one embodiment of a system according to the invention
  • FIG. 2 is a block diagram illustrating one implementation of the system in FIG. 1 ;
  • FIG. 3 is a perspective view of a servo-motor apparatus useful in this invention to illuminate a number of fiber bundles with a single energy source;
  • FIG. 4 is a schematic illustration of the disposition for examining human tissue such as a human breast
  • FIG. 5 is a schematic illustration of a planar imaging head useful in one embodiment of the invention.
  • FIG. 6 is one embodiment for the source detector arrangement on the imaging head shown in FIG. 5 ;
  • FIG. 7 is an illustration of a spherical imaging head useful in practicing the invention.
  • FIG. 8 is a block diagram of a detector channel useful in practicing the invention.
  • FIG. 9 is a graphical representation of one implementation of a timing scheme used in the system of FIG. 1 ;
  • FIG. 10 is a diagram illustrating the sequence of certain events in a multiple channel embodiment of the invention.
  • FIG. 11 is a schematic illustration of the physical arrangement of multiple detector channels used in a preferred embodiment of the invention.
  • FIG. 12 is a circuit diagram of one detector channel used in FIG. 11 ;
  • FIG. 13 is a circuit diagram of one implementation of the lock-in module used in FIG. 12 .
  • the objective of the invention is to provide a system and method capable to extract dynamics in properties of a scattering medium.
  • the use of the invention's system and method has several applications including, but not limited to, medical imaging applications.
  • medical imaging applications focus on tomographic imaging the dynamic properties of hemoglobin states and tissue using optical tomography, with an imaging source generating multiple wavelengths in the NIR region, it is appreciated that the invention is applicable to any medium that is able to scatter the propagating energy from any energy source, including external energy sources such as those sources located outside the medium and/or internal sources such as those energy sources located inside the medium.
  • other media includes, but are not limited to, medium from mammals, botanical life, aquatic life, or invertebrates; oceans or water masses; foggy or gaseous-atmospheres; earth strata; industrial materials; man-made or naturally occurring chemicals and the like.
  • Energy sources include, but are not limited to, non-laser optical sources like LED and high-pressure incandescent lamps and lasers sources such as laser diodes, solid state lasers such as titanium-sapphire laser and ruby laser, dye laser and other electromagnetic sources, acoustic energy, acoustic energy produced by optical energy, optical energy, and any combinations thereof
  • the means to detect the signal produced by the energy source is not limited to photodiode implementation discussed in one of the preferred embodiments further described herein.
  • Other detectors can be used with the principles of the present invention for the purpose of tomographic imaging the dynamic properties of a medium.
  • detectors include for example, but are not limited to, photodiodes, PIN diodes (PIN), Avalanche Photodiodes (APD), charge couple device (CCD), charge inductive device (CID), photo-multiplier tubes (PMT), multi-channel plate (MCP), acoustic transducers and the like.
  • the present invention builds upon previous disclosures in U.S. Pat. Nos. 5,137,355 (“the '355 patent”) entitled “Method of Imaging a Random Medium” (“the '355 patent”) and U.S. Pat. No. 6,081,322 (“the '322 patent”) entitled “NIR Clinical Opti-Scan System”, the disclosures of both the '355 and '322 patents are incorporated herein by reference. Disclosed in these patents is an approach to optical tomography, and the instrumentation required to accomplish the tomography. The modifications in the present invention provide fast data acquisition, and new imaging head designs. Fast data acquisition allows accurate sampling of dynamic features.
  • the modification in the imaging head allows accommodation of different size targets (e.g., breast); the stabilization of the target against motion artifacts; conforming the target to a simple well-defined geometry; and knowledge of source and detector positioning on or about the target. All of the enumerated features listed above for the imaging head is crucial for accurate image reconstruction.
  • the present invention uses detector circuitry that allows quick adaptation of the measurement range to the signal strength thereby increasing the over-all dynamic range.
  • “Dynamic range” for the purposes of this description means the ratio between the highest and lowest detectable signal. This makes the circuitry suitable for use with source-detector distances that can vary significantly during the data collection, thereby allowing fast data acquisition over wide viewing angles. For instance, we are aware that dynamic features of dense scattering media may be extractable from measurements using a single source and single detector at a fixed distance between each other. Depending on the implementation, such an arrangement could be made using a detector of relatively small dynamic range.
  • our invention allows the measurement of dynamics in optical properties of dense scattering media using source-detector pairs over a wide range of distances (e.g., greater than or about 5 cm). Such fall tomographic measurements allow for improved accuracy in image reconstruction.
  • the system of the present invention can also be operated using detector channels of low-dynamic range (e.g., 1:10.00) when detector fibers of a fixed distance from the source are being used for the measurement (e.g., the detector opposite the source).
  • detector channels of low-dynamic range e.g., 1:10.00
  • the data collection scheme of the present invention disclosed herein provides time-series of raw data sets that provide useful information about dynamic properties of the scattering medium without any further image reconstruction. For example, by displaying the raw data in a color mapping format, features can be extracted by sole visual inspection.
  • analysis algorithms of various types such as, but not limited to, linear and non-linear time-series analysis or pattern recognition methods can be applied to the series of raw data. The advantage of using these analytical methods is the improved capability to reveal dynamic signatures in the signals.
  • image reconstruction methods may be applied to the sets of raw data thereby providing time series of cross-sectional images of the scattering medium.
  • analysis methods of various types such as, but not limited to, linear and non-linear time-series analysis, filtering, or pattern recognition methods can be applied.
  • the advantage of using such analysis is the improved extraction of dynamic features and cross-sectional view, thereby increasing diagnostic sensitivity and specificity.
  • the invention reveals measurements of real-time spatiotemporal dynamics.
  • an image of dynamic optical properties of scattering medium such as, but not limited to, the vasculature of the human body in a cross-sectional view is provided.
  • the technology employs low cost, compact instrumentation that uses non-damaging near infrared optical sources and features several alternate imaging heads to permit investigation of a broad range of anatomical sites.
  • the principles of the present invention can be used in conjunction with contrast agents such as absorbing and fluorescent agents.
  • the present invention allows tie cross-sectional measurements of changes in optical properties due to variations in temperature. The advantage of this variant is seen, but not restricted to, the use of monitoring cryosurgery.
  • a system using the modified instrumentation and described methods of the instant invention is capable of producing cross-sectional images of real-time events associated with vascular reactivity in a variety of tissue structures (e.g., limbs, breast, head and neck).
  • tissue structures e.g., limbs, breast, head and neck.
  • Such measurements permit an in-depth analysis of local hemodynamic states that can be influenced by a variety of physiological manipulations, pharmacological agents or pathological conditions.
  • Measurable physiological parameters include identification of local dynamic variations in tissue blood volume, blood oxygenation, estimates of flow rates, and tissue oxygen consumption. It is specifically noted that measurements of several locations on the same medium can be taken. For example, measurements may be taken of the leg and arm areas of a patient at the same time. Correlation, of data between the different locations is available using the methods described herein.
  • the invention also provides both linear and non-linear time series analysis to reveal site specific functionality of the various components of the vascular tree.
  • the response characteristics of the major veins, arteries and structures associated with the microcirculation can be evaluated in response to a range of stimuli.
  • FIG. 1 illustrates one embodiment of the invention. Shown is a system 100 comprising medium 102 .
  • the medium can be any medium in which the propagation of the used source energy is strongly affected by scattering.
  • a source module 101 energy is directed to the medium 102 from which the exiting energy is measured by means of detector 106 , further discussed below.
  • detector 106 As previously discussed, there is a variety of sources, media, and detectors that may be used with the principles of the present invention. The following is a discussion of a sampling of such elements with the intention to describe how the invention is realized. In no way are these examples meant, nor do they intend to limit the invention to these implementations. A variation of elements as described herein may also utilize the principles of the present invention.
  • measurements of dynamics in the optical properties of the medium is accomplished by using optical source energy and performing rapid detection of the acoustic energy created by absorption processes in the medium.
  • optical source energy can be implemented using both pulsed and harmonic modulated light sources, the latter allowing for lock-in detection.
  • Detectors can be, but are not limited to, piezo-electric transducers such as PZT crystals or PVDF foils.
  • a timing and control facility 104 is used to coordinate source and detector operation. This coordination is further described below.
  • a device 116 provides acquisition and storage of the data measured by the detector 106 .
  • control and timing of the system's components is provided by a computer, which includes a central processor unit (CPU), volatile and non-volatile memory, data input and output ports, data and program code storage on fixed and removable media and the like. Each main component is described in greater detail below.
  • FIG. 2 illustrates another implementation of a preferred embodiment of the present invention. Shown is a system and method that incorporates at least one wavelength measurement. Depending upon the implementation, this measurement is accomplished by alternately coupling light from diode lasers into transmitting fibers arranged in a circular geometry.
  • a system 200 includes an energy source, which in this implementation includes one or more laser 101 .
  • a reference detector 202 is used to monitor the actual output power of laser 101 and is coupled to a data acquisition unit 116 .
  • Such laser may be a laser diode in the NIR region.
  • the laser is intensity modulated by a modulation means 203 for providing means of separation of background energy sources such as daylight.
  • the modulation signal is also sent to a phase shifter 204 whose purpose is described further below.
  • the light energy generated by the laser 101 is directed into an optical de-multiplexing device 300 further discussed in detail below. Using a rotating mirror 305 , the light is directed into one of several optical source fiber bundles 306 that are used to deliver the optical energy to the medium 102 .
  • a motor controller 201 is coupled to the de-multiplexing device 300 for controlling the motion of the rotating mirror 305 .
  • the motor controller 201 is also in communication with a timing control 104 for controlling the timing of the motion of mirror 305 .
  • the measuring head 206 comprises the common end of a bifurcated optical fiber bundle, whose split ends are formed by the source fiber bundle 306 and detector fiber bundle 207 .
  • Source fiber bundle 306 and detector fiber bundle 207 form a bulls eye geometry at the common end with the source fiber bundle in the center. In other embodiments, source and detector bundles are arranged differently at the common end (e.g., reversed geometry or arbitrary arrangement of the bundle filaments).
  • the common end of a bifurcated optical fiber bundle preferably comes in contact with the medium, however, this embodiment is not limited to contact with the medium. For example, the common ends may simply be disposed about the medium.
  • the signal is transmitted from the detector fiber bundle 207 to a detector unit 106 that comprises at least one detector channel 205 further described herein.
  • the detector channel 205 is coupled to the data acquisition unit 116 and the timing control unit 104 .
  • a phase shifter 204 may or may not be used, and is coupled to the detector unit 106 for the purposes of providing a reference signal for the purposes of filtering the signal received from bundle 207 .
  • FIG. 3 a device for the measurement of the dynamic properties of a scattering medium.
  • This measurement is performed by sequentially reflecting light 302 off of a rotatable front surface mirror 306 , mounted at a 45 degree angle to the incident source, into source fibers 306 arranged in a circular geometry about the rotating optic.
  • the rotation is done by a motor 308 with a shaft 307 to which the mirror is attached.
  • This embodiment has an advantage of enabling fast switching among the transmitting fibers. In particular, it provides the ability to introduce beam shaping optics between the reflective mirror and transmitting fibers thereby allowing fine adjustment of the illumination area available for coupling into the fibers.
  • Unit 300 Light from laser 101 is transmitted to unit 300 by means of transmitting optics 303 including, but not limited to, fiber optics and free propagating beams. Further beam shaping optics 301 may be used to optimize in coupling efficiency into the transmitting fibers. Units 303 and 301 are under mechanical fine adjustment in their position with respect to the mirror 309 .
  • Motor 308 is operated under control of motion control 201 to allow for precise positioning and timing.
  • motion control 201 By this means, it is possible to operate the motor under complex motion protocols such as in a start-stop fashion where the motor stops at a desired location thereby allowing the stable coupling of light into a transmitting fiber bundle. After the measurement at this source location is performed, the motor moves on to the next transmitting fiber.
  • Motion control is in two-way communication with the timing control 104 thereby allowing precise timing of this procedure.
  • Motion control allows the assignment of relative and/or absolute mirror positions allowing for precise alignment of the mirror with respect to the physical location of the fiber bundle.
  • the mirror 306 is surrounded by a cylindrical shroud 309 in order to shield off stray light to prevent cross-talk.
  • the shroud comprises an aperture 310 through which the light beam 302 passes toward the transmitting fiber. It is recognized and incorporated herein other schemes which may be used,(e.g., use of a fiber-optic switching device) to sequentially couple light into the transmitting fibers.
  • fast switching of source positions is accomplished by using a number of light sources, each coupled into one of the transmitting fibers 306 which can be turned on and of each independently by electronic means.
  • the device employs the servo-motor control system 308 in FIG. 3 with beam steering optics, described above, to sequentially direct optical energy emerging from the source optics onto about 1 mm diameter optical fiber bundles 306 , which are mounted in a circular array in the multiplexing input coupler 300 .
  • the transmitting optical fiber bundles 306 which are typically 2-3 meters in length are arranged in the form of an umbilical and terminate in the imaging head 206 .
  • the apparatus of the present invention required for time-series imaging employs the value of using a geometrically adaptive measurement head or imaging head.
  • the imaging head of the present invention provides features that include, but are not limited to, 1) accommodating different size targets (e.g., breast); 2) stabilizing the target against motion artifacts; 3) conforming the target to well-defined geometry; and 4) to provide exact knowledge of locations for sources and detectors. Stability and a known geometry both contribute to the use of efficient numerical analysis schemes.
  • imaging head for data collection there are several different embodiments of the imaging head for data collection that may utilize the principles of the present invention.
  • the use of an iris imaging head previously disclosed in the '322 and '355 patents which are incorporated by reference in this disclosure, may be used with the principles of the present invention.
  • imaging heads Described below are two exemplary imaging heads with the understanding that the invention may or may not use any type of imaging head, and if an imaging head is used, it would provide the features previously described.
  • the iris unit can be employed as a parallel array of irises 402 , 404 , 406 enabling volume imaging studies.
  • FIG. 4 illustrates how this can be configured for studying a medium 410 , in this example a human breast, using an imaging head 408 .
  • the medium used in the present invention can be any medium, which allows scattering of energy.
  • the imaging head illustrated in FIG. 5 is a flexible pad configuration.
  • This planar imaging unit functions as a deformable array and is well suited to investigate body structures too large to permit transmission measurements (e.g., head and neck, torso, and the like).
  • optical measurements are made in a back-reflection mode.
  • Optical fiber bundles 502 originating from the optical multiplexing input coupler 112 (described elsewhere) terminate at the deformable array or flexible pad 500 .
  • the pad can be made of any flexible material such as black rubber or the like.
  • the optical fiber bundles may be bifurcated and have ends 504 that both transmit and receive light.
  • More than one pad may or may not be used, although an additional pad is not necessary for the purpose of the present invention, or for measurement application to other portions of the medium or to the same medium.
  • both pads maybe applied to the same breast having one pad above and one pad below the breast.
  • one pad maybe applied to the right breast by having the pad deformed around the breast.
  • the other pad may be applied to the left breast. This configuration would allow both breasts to be examined at the same time.
  • information may be correlation between the data collected from the two different members of the body.
  • the invention can be applied to other media and is not limited to portions of the human body. Thus, correlation between different media may be collected using this technique.
  • the additional pad would have similar functions as the pad previously described and would have optical fiber bundles 503 , flexible pad 505 , and bifurcated optical fiber bundle ends 501 similar to the previous pad described.
  • the array itself can be deformed to conform to the surface of a curved medium to be imaged (e.g. portion of the torso).
  • the deformable array optical energy source and receiver design includes, depending on the implementation, a 7 ⁇ 9 array (63 total bundles) of optical fiber bundles as illustrated in FIG. 6 . In one variant, each bundle is typically 3 mm in diameter.
  • eighteen (18) of the sixty-three (63) fiber bundles may be arranged in an array to serve as both optical energy sources or energy transmitters, and receivers to sequentially deliver light to a designated target and receive emerging optical energy.
  • the remaining forty-five (45) fiber bundles act only as receivers of the emerging optical energy.
  • the geometry of the illumination array is not arbitrary.
  • the design shown in FIG. 6 as an exemplary illustration has been configured, as have other implementations, to minimize the subsequent numerical effort required for data analysis while maximizing the source-density covered by the array.
  • the fiber bundles are arranged in an alternating pattern as described by FIG. 6 and shown here with the symbols “X” and “0”.
  • a pattern of 00X000X00, X000X000X can be used on the imaging head.
  • ‘X’ denotes a source/receiver fiber bundle
  • ‘0’ is a receiver only.
  • FIG. 6 indicates 2D imaging planes formed by multiple source/detector positions along a line that can be used with this particular pattern.
  • the labels refer to the numbers of sources/detectors found along those lines of optical fiber ends on the pad using the following nomenclature: “S” followed by a number indicates the number of source positions along that line; “D” followed by a number indicates the number of detection points along that line. For instance; “S3-D3” indicates an imaging plane formed by three source positions and three detection points.
  • the design allows for the independent solution of two dimensional (2-D) image recovery problems from an eighteen (18) point source measurement.
  • a composite three dimensional (3-D) image can be computed from super-position of the array of 2-D images oriented perpendicular to the target surface.
  • Another advantage of this geometry is that it readily permits the use of parallel computational strategies without having to consider the entire volume under examination.
  • each reconstruction data set is derived from a single linear array of source-detector fibers, thereby enabling solution of a 2-D problem without imposing undue physical approximations.
  • the number of source-detector fibers belonging to an array can be varied. Scan speeds attainable with the 2-D array illustrated in FIG. 6 are the same as for other imaging heads with 2-D arrays since the scan speed depends only on the properties of the input coupler. Thus, faster scan speed are available for the creation of a 3-D image.
  • FIG. 7 is an imaging head based on a “Hoberman” sphere geometry.
  • the geometry is based on the intersection of a cube and an octahedron, which makes a folding polyhedron called a trapezoidal icosatetrahedron.
  • This structure has been modified and implemented in a form of an imaging head of a hemispherical geometry.
  • it is appropriate to use design features of smoothly varying surfaces based on the Hoberman concept of expanding structures.
  • other polygonal or spherical-type shapes may also be used with the principles of the present invention for other imaging head designs. Adjustment of the device in FIG.
  • Imaging head 700 illustrates one example of modification to the “Hoberman” geometry.
  • a receptacle for the fiber bundles 701 is disposed about imaging head 700 .
  • Target volume 702 is where the medium would enter the imaging head in this implementation.
  • This geometry is well suited for the investigation of certain tissues such as the female breast or the head.
  • attachment of optical fibers to the vertices of the hemisphere allows for up a seventeen (17) source by seventeen (17) detector measurement.
  • the folding structure can be extended to accommodate a more “tear drop” or “bullet” shape of the target medium by attaching additional circular iris-like structures on top that expand and contract with the hemisphere.
  • FIG. 7 shows the combination of the hemisphere with one top iris comprising receptacles for 8 additional fiber bundles leading to an overall number of 25 source by 25 detector positions at the main vertices for this configuration. More than one iris can be attached to the top of the hemisphere. The diameter of the additional top irises may or may not differ from the hemisphere diameter. The detectors or energy receivers may be disposed about the imaging head and the detectors are located on the inner aspect of the expanding imaging head. Additional fiber bundles can be attached to the interlocking joints, permitting up to a 49 source by 49 detector measurement for the hemisphere only and up to 16 source/detector positions per added iris.
  • light collected from the target medium is measured by using any of a number of optical detection schemes.
  • One embodiment uses a fiber-taper, which is bonded to a charged coupled detector (CCD) array.
  • CCD charged coupled detector
  • the front end of the fiber taper serves to receive light exiting from the collection fibers.
  • These fibers are preferably optical fibers, but can be any means that allows the transmission and reception of signals.
  • the back end of the fiber taper is bonded to a 2-D charge-coupled-detector (CCD) array.
  • CCD charge-coupled-detector
  • An alternate detection scheme employs an array of discrete photo detectors, one for each fiber bundle. This unit can be operated in a phase lock mode thereby allowing for improved rejection of ambient light signals and the discrimination of multiple simultaneously operated energy sources.
  • the following features characterize the detector system: scalable multi-channel design (up to 32 detector channels per unit); high detection sensitivity (below 10 pW); large dynamic range (1:10 6 minimum); multi-wavelength operation; ambient light immunity; and fast data acquisition (order of 100 Hz all-channel simultaneous capture rate).
  • the detector system uses photodiodes and a signal recovering technique involving electronic gain switching and phase sensitive detection (lock-in amplification) for each detector fiber (in the following referred to as detection or detector channels) to ensure a large dynamic range at the desired data acquisition rate.
  • the phase sensitive signal recovery scheme not only suppresses electronic noise to a desired level but also eliminates disturbances given by background light and allows simultaneous use of more than one energy source. Separation of signals from simultaneously operating sources can be achieved, as long as the different signals are encoded in sufficiently separated modulation frequencies. Since noise reduction techniques are based on the reduction of detection bandwidth, the system is designed to maintain the desired rate of measurements.
  • a sample-and-hold circuit (S/H) is used for each detection channel output.
  • the analog signals provided by the detector channels are sampled, digitized and stored using the data acquisition system 116 .
  • One aspect is the flexibility and scalability of the detection instrument. Not only are the detector channels organized in single, identical modules, but also the phase detection stages, each containing two lock-in amplifiers, are added as cards. In this way, an existing setup can easily be upgraded in either the number of detector channels and/or the number of wavelengths used (up to four) by cloning parts of the existing hardware.
  • FIG. 8 shows the block diagram of one implementation of a detector channel.
  • two energy sources are used.
  • the signal After detecting the light at the optical input 801 by a photo detector 802 the signal is fed to a transimpedance amplifier 803 .
  • PTA Programmable Transimpedance Amplifier
  • the signal is subsequently amplified by a Programmable Gain Amplifier (PGA ⁇ whose gain can be set externally by means of digital signals 814 . This allows for additional gain for the lowest signal levels (e. g., in one implementation pW-nW) thereby increasing the dynamic range of the detector channel.
  • PGA ⁇ Programmable Gain Amplifier
  • At least one energy source is used and the signal is sent to at least one of lock-in amplifiers (LIA) 805 , 809 .
  • Each lock-in amplifier comprises an input 808 , 812 for the reference signal generated by phase shifter 204 from FIG. 2 .
  • the demodulated signal is appropriately boosted in gain by means of a programmable gain amplifier (PGA) 806 , 810 in order to maximize noise immunity during further signal transmission and to improve digital resolution when being digitized.
  • PGA programmable gain amplifier
  • the gain of PGA 806 , 810 is set by digital signals 815 .
  • a sample-and-hold circuit (S/H) 807 , 811 is used for freezing the signal under digital timing by means of signal 816 for purposes described herein.
  • the signal 815 is sent to PGA 806 , 810 in parallel. In one embodiment, the signal 816 is sent to 807 , 811 in parallel.
  • the analog signal provided by each of the channel outputs is sampled by a data acquisition system 116 .
  • PC extension boards might be used for this purpose.
  • PC extension boards also provide the digital outputs that control the timing of functions such as gain settings and sample-and-hold.
  • FIG. 9 shows one improvement of the invention over other timing schemes.
  • a schedule according to 905 has to be implemented.
  • the implementation in FIG. 9 illustrates one use of a silicon photo-diode in process 904 , which can be replaced by various detectors previously mentioned.
  • a time series of data is acquired for a fixed source position. After finishing this task, the source is moved 902 with respect to the target 901 and another series of data is collected. Measurements are performed in this fashion for all source positions.
  • Every image 903 of the resulting time series of reconstructed images is reconstructed from data sets merged together from the data for each source position.
  • This schedule does not allow real-time capture of all physiologic processes in the medium and therefore only applies to certain modes of investigation.
  • the timing scheme for the invention very much improves on this situation.
  • a schedule indicated by 904 is performed.
  • the source position is switched fast compared to the dynamic features of interest and instantaneous multi-channel detection is performed at each source position.
  • Images 903 are then reconstructed from data sets, which represent an instant state of the dynamic properties of the medium. Only one time series of full data sets (i. e., all source positions and all detector positions) is being recorded. Real time measurement of fast dynamics (e.g., faster than I Hz) of the medium is provided by the invention.
  • FIG. 10 shows one embodiment of a detailed schedule and sequence of the system tasks 1001 involved in collecting data at a source position and the proceeding of this process in time 1002 .
  • Task 1003 is the setting of the optical de-multiplexer to a destined source position and setting the detectors to the appropriate gain- settings.
  • the source position is illuminated for a period of time 1004 , during which the lock-in amplifiers settle 1005 .
  • the signal is held for a period of time 1007 , during which all channels are read out by the data acquisition. It is worthwhile noticing that during reading out the S/H, other tasks, like moving the optical source, setting the detector gains for the new source position, and settling of the lock-in, are being scheduled. This increases greatly the achievable data acquisition rate of the instrument.
  • FIG. 11 This concept of a modular system is further illustrated in FIG. 11 .
  • Up to thirty-two (32) detector modules 1100 (each with 2 lock-in modules each for two modulation frequencies) are arranged using an enclosure 1102 .
  • the cabinet also can carry up to two phase shifting modules 1104 , 1106 , each containing two digital phase shifter under computer control.
  • the ability to adjust the reference phase with respect to the signal becomes necessary since unavoidable phase shifts in the signal may lead to non-optimum lock-in detection or can even result in a vanishing output signal.
  • Organization of data, power supply and signal lines is provided by means of two back planes 1108 , 1110
  • the detector system design illustrated in FIG. 8 allows one cabinet to operate at a capacity of 32 detectors with four different sources requiring 128 analog to digital circuit (ADC)-board input channels.
  • the upper 1108 and the lower 1110 back plane are of identical layout and have to be linked in order to provide the appropriate distribution of supply-, control- and signal voltages. This is achieved using a 6U-module fitting both planes from the backside, that provides the necessary electric linking paths, and interfaces for control- and signal lines.
  • FIG. 12 shows the schematic of one implementation of a channel module.
  • a silicon photo-diode 1206 is used as the photo-detector.
  • a Programmable Transimpedance Amplifier (PTA) 1201 is formed by an operational amplifier 1204 , resistors 1201 and 1202 and an electronic switch 1205 , the latter of which is realized using a miniature relay. Other forms of electronic switches such as analog switches might be used.
  • Relay 1205 is used to connect or disconnect 1203 from the circuit thereby changing the transimpedance value of 1201 .
  • a high-pass filter (R2, C5) is used to AC-couple the subsequent programmable gain instrumentation amplifier IC 2 (Burr Brown PGA202) in order to remove DC offset.
  • the board-to-board connectors for the two lock-in-modules are labeled as “slot A” 1210 and “slot B” 1212 .
  • the main connector to the backplane is a 96-pole DIN plug 1220 .
  • FIG. 13 illustrates the electric circuit of the lock in modules 1210 , 1212 .
  • the signal is subdivided and passed to two identical lock-in-amplifiers, each of which gets one particular reference signal according to the sources used in the experiment.
  • the signal is first buffered IC 1 , IC 7 (AD LF 111) and then demodulated using an AD630 double-balanced mixer IC 2 , IC 8 .
  • the demodulated signal passes through an active 4-pole Bessel-type filter IC 3 , IC 4 , IC 9 , IC 10 (Burr Brown UAF42).
  • a Bessel-type filter has been chosen in order to provide fastest settling of the lock-in amplifier for a given bandwidth. Since a Bessel-filter shows only slow stopband-transition, a 4-pole filter is being used to guarantee sufficient suppression of cross talk between signals generated by different sources (i.e. of different modulation frequency).
  • the filter has its 3 dB point at 140 Hz, resulting in 6 ms settling time for a step response ( ⁇ 1% deviation of actual value).
  • the isolation of frequencies separated by 1 kHz is 54 dB.
  • the filters are followed by a programmable gain amplifier IC 5 , IC 11 , whose general function has been described above.
  • the last stage is formed by a sample-and-hold chip (S/H) IC 6 , IC 12 (National LF398).
  • S/H sample-and-hold chip
  • phase sensitive detection can be achieved with digital methods using digital signal processing (DSP) components and algorithms.
  • DSP digital signal processing
  • an analog-to-digital converter is used for each detector channel thereby improving noise immunity of the signals.

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Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20090069695A1 (en) * 2006-03-17 2009-03-12 Koninklijke Philips Electronics N.V. Device for imaging a turbid medium
US20100234727A1 (en) * 2006-03-31 2010-09-16 Mayuka Yoshizawa Mammographic apparatus
US8892192B2 (en) 2012-11-07 2014-11-18 Modulated Imaging, Inc. Efficient modulated imaging
US9220412B2 (en) 2009-11-19 2015-12-29 Modulated Imaging Inc. Method and apparatus for analysis of turbid media via single-element detection using structured illumination
USD763938S1 (en) 2014-04-02 2016-08-16 Cephalogics, LLC Optical sensor array
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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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Citations (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4810875A (en) * 1987-02-02 1989-03-07 Wyatt Technology Corporation Method and apparatus for examining the interior of semi-opaque objects
US5137355A (en) * 1988-06-08 1992-08-11 The Research Foundation Of State University Of New York Method of imaging a random medium
US5351677A (en) * 1991-04-24 1994-10-04 Olympus Optical Co., Ltd. Medical system having object information reproduction means for palpation
US5353799A (en) * 1991-01-22 1994-10-11 Non Invasive Technology, Inc. Examination of subjects using photon migration with high directionality techniques
US5365066A (en) * 1989-01-19 1994-11-15 Futrex, Inc. Low cost means for increasing measurement sensitivity in LED/IRED near-infrared instruments
US5386819A (en) * 1990-03-29 1995-02-07 Olympus Optical Co., Ltd. Method and apparatus for inhibiting a scattered component in a light having passed through an examined object
US5408093A (en) * 1992-08-31 1995-04-18 Hitachi, Ltd. Optical computed tomography equipment having image inverting optical device
US5555087A (en) * 1993-06-15 1996-09-10 Fuji Photo Film Co., Ltd. Method and apparatus for employing a light source and heterodyne interferometer for obtaining information representing the microstructure of a medium at various depths therein
US5625458A (en) * 1994-11-10 1997-04-29 Research Foundation Of City College Of New York Method and system for imaging objects in turbid media using diffusive fermat photons
GB2311854A (en) 1995-11-17 1997-10-08 Hitachi Ltd Instrument for optical measurement of living body
US5676141A (en) * 1993-03-31 1997-10-14 Nellcor Puritan Bennett Incorporated Electronic processor for pulse oximeters
US5820558A (en) 1994-12-02 1998-10-13 Non-Invasive Technology, Inc. Optical techniques for examination of biological tissue
US5865754A (en) * 1995-08-24 1999-02-02 Purdue Research Foundation Office Of Technology Transfer Fluorescence imaging system and method
US5994690A (en) * 1997-03-17 1999-11-30 Kulkarni; Manish D. Image enhancement in optical coherence tomography using deconvolution
US6081322A (en) * 1997-10-16 2000-06-27 Research Foundation Of State Of New York NIR clinical opti-scan system
US6091983A (en) * 1997-02-07 2000-07-18 Alfano; Robert R. Imaging of objects in turbid media based upon the preservation of polarized luminescence emitted from contrast agents
US6108576A (en) * 1996-03-18 2000-08-22 The Research Foundation Of City College Of New York Time-resolved diffusion tomographic 2D and 3D imaging in highly scattering turbid media
US6282438B1 (en) * 1994-10-06 2001-08-28 Hitachi, Ltd. Optical system for measuring metabolism in a body and imaging method
US6377842B1 (en) * 1998-09-22 2002-04-23 Aurora Optics, Inc. Method for quantitative measurement of fluorescent and phosphorescent drugs within tissue utilizing a fiber optic probe
US6485413B1 (en) * 1991-04-29 2002-11-26 The General Hospital Corporation Methods and apparatus for forward-directed optical scanning instruments
US6526309B1 (en) * 1995-01-03 2003-02-25 Non-Invasive Technology, Inc. Transcranial in vivo examination of brain tissue
US6590651B1 (en) * 1998-05-19 2003-07-08 Spectrx, Inc. Apparatus and method for determining tissue characteristics
US6608717B1 (en) * 1999-01-29 2003-08-19 Colorado State University Research Foundation Optical coherence microscope and methods of use for rapid in vivo three-dimensional visualization of biological function

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH04249746A (ja) * 1990-12-31 1992-09-04 Shimadzu Corp 断層像再構成法
US5762609A (en) * 1992-09-14 1998-06-09 Sextant Medical Corporation Device and method for analysis of surgical tissue interventions
JP3433508B2 (ja) * 1993-12-01 2003-08-04 浜松ホトニクス株式会社 散乱吸収体計測方法及び散乱吸収体計測装置
WO1998024361A2 (en) * 1996-12-03 1998-06-11 Koninklijke Philips Electronics N.V. Method and apparatus for imaging an interior of a turbid medium
DE69822439T2 (de) * 1997-11-22 2005-01-20 Koninklijke Philips Electronics N.V. Verfahren zur auffindung eines körpers in einem trüben medium
JP4733265B2 (ja) * 1998-02-11 2011-07-27 ノン−インヴェイシヴ テクノロジイ，インク． 脳組織の画像形成および特徴表示

Patent Citations (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4810875A (en) * 1987-02-02 1989-03-07 Wyatt Technology Corporation Method and apparatus for examining the interior of semi-opaque objects
US5137355A (en) * 1988-06-08 1992-08-11 The Research Foundation Of State University Of New York Method of imaging a random medium
US5365066A (en) * 1989-01-19 1994-11-15 Futrex, Inc. Low cost means for increasing measurement sensitivity in LED/IRED near-infrared instruments
US5386819A (en) * 1990-03-29 1995-02-07 Olympus Optical Co., Ltd. Method and apparatus for inhibiting a scattered component in a light having passed through an examined object
US5353799A (en) * 1991-01-22 1994-10-11 Non Invasive Technology, Inc. Examination of subjects using photon migration with high directionality techniques
US5664574A (en) * 1991-01-22 1997-09-09 Non-Invasive Technology, Inc. System for tissue examination using directional optical radiation
US5351677A (en) * 1991-04-24 1994-10-04 Olympus Optical Co., Ltd. Medical system having object information reproduction means for palpation
US6485413B1 (en) * 1991-04-29 2002-11-26 The General Hospital Corporation Methods and apparatus for forward-directed optical scanning instruments
US5408093A (en) * 1992-08-31 1995-04-18 Hitachi, Ltd. Optical computed tomography equipment having image inverting optical device
US5676141A (en) * 1993-03-31 1997-10-14 Nellcor Puritan Bennett Incorporated Electronic processor for pulse oximeters
US5555087A (en) * 1993-06-15 1996-09-10 Fuji Photo Film Co., Ltd. Method and apparatus for employing a light source and heterodyne interferometer for obtaining information representing the microstructure of a medium at various depths therein
US6282438B1 (en) * 1994-10-06 2001-08-28 Hitachi, Ltd. Optical system for measuring metabolism in a body and imaging method
US5625458A (en) * 1994-11-10 1997-04-29 Research Foundation Of City College Of New York Method and system for imaging objects in turbid media using diffusive fermat photons
US5820558A (en) 1994-12-02 1998-10-13 Non-Invasive Technology, Inc. Optical techniques for examination of biological tissue
US6526309B1 (en) * 1995-01-03 2003-02-25 Non-Invasive Technology, Inc. Transcranial in vivo examination of brain tissue
US5865754A (en) * 1995-08-24 1999-02-02 Purdue Research Foundation Office Of Technology Transfer Fluorescence imaging system and method
GB2311854A (en) 1995-11-17 1997-10-08 Hitachi Ltd Instrument for optical measurement of living body
US6108576A (en) * 1996-03-18 2000-08-22 The Research Foundation Of City College Of New York Time-resolved diffusion tomographic 2D and 3D imaging in highly scattering turbid media
US6091983A (en) * 1997-02-07 2000-07-18 Alfano; Robert R. Imaging of objects in turbid media based upon the preservation of polarized luminescence emitted from contrast agents
US5994690A (en) * 1997-03-17 1999-11-30 Kulkarni; Manish D. Image enhancement in optical coherence tomography using deconvolution
US6081322A (en) * 1997-10-16 2000-06-27 Research Foundation Of State Of New York NIR clinical opti-scan system
US6590651B1 (en) * 1998-05-19 2003-07-08 Spectrx, Inc. Apparatus and method for determining tissue characteristics
US6377842B1 (en) * 1998-09-22 2002-04-23 Aurora Optics, Inc. Method for quantitative measurement of fluorescent and phosphorescent drugs within tissue utilizing a fiber optic probe
US6608717B1 (en) * 1999-01-29 2003-08-19 Colorado State University Research Foundation Optical coherence microscope and methods of use for rapid in vivo three-dimensional visualization of biological function

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20090069695A1 (en) * 2006-03-17 2009-03-12 Koninklijke Philips Electronics N.V. Device for imaging a turbid medium
US20100234727A1 (en) * 2006-03-31 2010-09-16 Mayuka Yoshizawa Mammographic apparatus
US8406846B2 (en) * 2006-03-31 2013-03-26 Shimadzu Corporation Mammographic apparatus
US9220412B2 (en) 2009-11-19 2015-12-29 Modulated Imaging Inc. Method and apparatus for analysis of turbid media via single-element detection using structured illumination
US9277866B2 (en) 2009-11-19 2016-03-08 Modulated Imaging, Inc. Method and apparatus for analysis of turbid media via single-element detection using structured illumination
US8892192B2 (en) 2012-11-07 2014-11-18 Modulated Imaging, Inc. Efficient modulated imaging
US9883803B2 (en) 2012-11-07 2018-02-06 Modulated Imaging, Inc. Efficient modulated imaging
US10342432B2 (en) 2012-11-07 2019-07-09 Modulated Imaging, Inc. Efficient modulated imaging
USD763938S1 (en) 2014-04-02 2016-08-16 Cephalogics, LLC Optical sensor array
USD763939S1 (en) 2014-04-02 2016-08-16 Cephalogics, LLC Optical sensor array liner with optical sensor array pad
US9599697B2 (en) 2014-04-15 2017-03-21 The Johns Hopkins University Non-contact fiber optic localization and tracking system

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