WO2000013578A1 - Sondes a ballonnet pour endoscope a infrarouge - Google Patents

Sondes a ballonnet pour endoscope a infrarouge Download PDF

Info

Publication number
WO2000013578A1
WO2000013578A1 PCT/US1999/020321 US9920321W WO0013578A1 WO 2000013578 A1 WO2000013578 A1 WO 2000013578A1 US 9920321 W US9920321 W US 9920321W WO 0013578 A1 WO0013578 A1 WO 0013578A1
Authority
WO
WIPO (PCT)
Prior art keywords
collection
probe
fiber
distal
balloon
Prior art date
Application number
PCT/US1999/020321
Other languages
English (en)
Inventor
Jenny E. Freeman
Charles R. Lambert
Edgard N. Lewis
Michael J. Hopmeier
Original Assignee
Hypermed Imaging, Inc.
United States Government As Represented By Secretary Of The Department Of Health And Human Services
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Hypermed Imaging, Inc., United States Government As Represented By Secretary Of The Department Of Health And Human Services filed Critical Hypermed Imaging, Inc.
Priority to AU59086/99A priority Critical patent/AU5908699A/en
Publication of WO2000013578A1 publication Critical patent/WO2000013578A1/fr

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/0059Measuring for diagnostic purposes; Identification of persons using light, e.g. diagnosis by transillumination, diascopy, fluorescence
    • A61B5/0082Measuring for diagnostic purposes; Identification of persons using light, e.g. diagnosis by transillumination, diascopy, fluorescence adapted for particular medical purposes
    • A61B5/0084Measuring for diagnostic purposes; Identification of persons using light, e.g. diagnosis by transillumination, diascopy, fluorescence adapted for particular medical purposes for introduction into the body, e.g. by catheters
    • A61B5/0086Measuring for diagnostic purposes; Identification of persons using light, e.g. diagnosis by transillumination, diascopy, fluorescence adapted for particular medical purposes for introduction into the body, e.g. by catheters using infrared radiation
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/0059Measuring for diagnostic purposes; Identification of persons using light, e.g. diagnosis by transillumination, diascopy, fluorescence
    • A61B5/0075Measuring for diagnostic purposes; Identification of persons using light, e.g. diagnosis by transillumination, diascopy, fluorescence by spectroscopy, i.e. measuring spectra, e.g. Raman spectroscopy, infrared absorption spectroscopy

Definitions

  • the present invention relates to probes useful in endoscopy and other procedures, and more particularly to balloon probes adapted to obtain spectroscopic information in the infrared spectral region.
  • the invention also relates to methods that utilize these probes to analyze a surface of interest in connection with the diagnosis and treatment of disease.
  • Endoscopes have proved useful in the examination of internal surfaces, in connection with various surgical and diagnostic procedures.
  • conventional endoscopes such as colonoscopes, gastroscopes, bronchoscopes, and angioscopes
  • colonoscopes such as colonoscopes, gastroscopes, bronchoscopes, and angioscopes
  • angioscopes are limited in their ability to detect all pathology present or provide unequivocal identification of abnormalities.
  • These devices typically collect reflected visible light from a lumen, which may be expanded with water or gas, for simple visual evaluation of the tissue surface of interest. If a definitive diagnosis of the type of pathology or disease present in the tissue is needed, a tissue specimen is typically removed or biopsied and submitted for pathologic testing.
  • the biopsy process increases the risk of complications to the patient, such as hemorrhage, infection, and possible perforation of the organ or vessel under examination.
  • endoscopes that detect fluorescence emitted following excitation of tissue with a radiation source have also been described.
  • One such device includes a visible light source, an optional endoscopic probe, optical sensors, a filter, a detector, and a display monitor.
  • One or two wavelengths of visible light preferably blue and red/near-infrared light, is directed to the tissue of interest, and remittance and autofluorescence is then detected, integrated/processed and displayed ( U. S. Patent No. 5,590,660 to MacAulay).
  • This device does not incorporate balloons into the probes to facilitate optical coupling, to allow infrared-based evaluation of the diseased tissue.
  • Another device useful for diagnosing the condition of Gl tissue, utilizes fiber optics to detect emitted fluorescence following excitation radiation treatment (U.S. Patent No 5,421,337 to Richards-Kortum).
  • devices which detect precancerous lesions using a mercury arc lamp endoscope U.S. Patent No. 5,647,368 to Zeng
  • devices which monitor and determine pre-existing physical properties of an organ by excitation with UV light U.S. Patent No. 5,456,252 to Vari
  • devices which determine bilirubin concentration in tissue using reflectance spectroscopy U.S. Patent No 5,353,790 to Jacques
  • these devices do not combine balloon endoscopes with infrared radiation to detect diseased tissue.
  • Balloon catheters like endoscopes, have been routinely used for diagnostics and treatment.
  • Typical uses of conventional balloon catheters include procedures such as angioplasty and embolectomy.
  • these conventional balloon devices could not be used in procedures in which infrared light is emitted in close proximity or directly onto a tissue surface, followed by collection of the light reflected or emitted from the tissue of interest, due to moisture and fluids in the surrounding environment.
  • the fiber(s) is anchored within the catheter so that there is an appropriate distance or space between the output end of the f ⁇ ber(s) and the tip of the shield.
  • the intervening space may be filled with fluid, optical surfaces may be optically contacted, or they may be anti-reflection coated to reduce reflections and maximize transmitted light.
  • the catheter may be inserted into a blood vessel and the shield brought into contact with a plaque or obstruction site.
  • the protective optical shield mechanically displaces blood at the region to be analyzed and also protects the distal tip of the optical f ⁇ ber(s) from intra- arterial contents. By locally displacing blood, the shield allows viewing of the tissue of interest without the need for a purge or flush.
  • the optical shield may be in the form of glass, fused silica, sapphire or other optically transparent material.
  • a flexible balloon over the tip of the probe may also be used as an optical shield. A different balloon may be used to provide an anchor point for positioning the catheter during use.
  • the shields of these devices protect a probe tip from blood contaminants
  • the use of a single balloon to both anchor and protect the tip of the probe from infrared opaque contaminants, which simultaneously allows optical coupling in the infrared region between the probe tip and the tissue surface has not previously been described.
  • the Kittrell devices are designed for use with visible light.
  • probes incorporating two anchoring balloons which allow the evacuation of a lumen and its subsequent filling with an infrared lucent coupling fluid are also not described.
  • Probes include an IR-transmitting single or multiple fiber endoscope, which is connected to a high resolution spectrometer. Infrared spectra are collected and used for diagnosis.
  • the use of spectroscopy with a fiberoptic endoscope allows the collection of high resolution information in the infrared spectral region from diseased tissue.
  • the present invention allows for rapid and accurate analysis of an organ, despite the presence of moisture, without the need for a tissue biopsy and its potential complications, such as hemorrhage, perforation and infection.
  • the anchoring balloons in conjunction with the endoscopic probes, collection of diagnostic spectra, particularly infrared radiation, in the lumen of a vessel or organ is even further enhanced.
  • the novel balloon configurations displace any opaque fluids which may be present and allow optical coupling of the probe to the tissue of interest.
  • multiple fibers may be paired with hyperspectral imaging techniques.
  • Each fiber's data may be processed to provide a single pixel.
  • the pixels produced by each individual fiber may be incorporated into an imaging array and/or translated into an image or other display optimized so that it may be readily interpreted or read by the user.
  • one embodiment of the invention is directed to a probe device which is useful for collecting infrared radiation from a surface of interest.
  • the collected radiation is analyzed to provide information about the tissue surface.
  • the probe device of this embodiment comprises a collection fiber which has a proximal end, a distal collection end opposite the proximal end adapted to collect infrared radiation, and an infrared conductive core located between the proximal end and the distal collection end.
  • a sheath is provided which receives and surrounds at least a portion of the collection fiber.
  • a first anchoring balloon is preferably disposed on the sheath. The distal collection end of the collection fiber may be nested inside or disposed inside the balloon during operation.
  • the first anchoring balloon may be disposed on the sheath between the proximal end and the distal collection end of the fiber and a second anchoring balloon may be disposed on a portion of the sheath that extends distally past the distal collection end of the collection fiber.
  • the void created between the balloons and the lumen wall may be filled with an infrared lucent fluid, displacing any infrared opaque fluids. This allows optical coupling of the collection end of the probe to the tissue surface, and protects the end of the probe from contamination.
  • Another embodiment is directed to a probe device having a plurality of collection fibers adapted to collect light, which is preferably infrared light.
  • the probe device of this embodiment comprises an imaging collection fiber bundle comprising a plurality of collection fibers, each of the plurality of collection fibers comprising a proximal end, a distal collection end opposite the proximal end, and a conductive core located between the proximal end and the distal collection end.
  • a first anchoring balloon is disposed on the fiber bundle; preferably it is disposed so that the distal collection ends of the plurality of collection fibers are disposed inside the balloon. Alternately, it may have the two balloon configuration previously described.
  • Another embodiment is directed to an endoscopic probe having a collection fiber which has a proximal end, a distal collection end opposite the proximal end adapted to collect infrared light, and a conductive core located between the proximal end and the collection end.
  • the probe also has an illumination fiber having a distal illumination end adjacent the distal collection end of the collection fiber, and a proximate end coupled to the illumination source.
  • An infrared lucent anchoring balloon is positioned on the probe such that the distal collection end of the collection fiber and the illumination end of the illumination fiber may be disposed in the balloon.
  • the illumination fiber preferably provides infrared light.
  • Another embodiment of the invention is directed to an endoscopic probe comprising a toroidally-shaped anchoring balloon, having a central hole therethrough, and a collection fiber adapted to collect infrared radiation.
  • the fiber has a distal collection end disposed inside the central hole of the balloon.
  • the present invention is also directed to methods for obtaining information about a surface of interest.
  • One such method comprises the steps of positioning a probe adjacent to the surface of interest, collecting infrared light using the probe, transmitting the infrared light from the surface to analyzing means, and analyzing the infrared light to determine one or more properties of the surface.
  • the probe preferably comprises a collection fiber, the collection fiber comprising a proximal end, a distal collection end opposite the proximal end adapted to collect infrared light, and an infrared conductive core located between the proximal end and the distal collection end, and at least one anchoring balloon disposed on the probe.
  • Another embodiment is directed to a method for obtaining information about a surface of interest, comprising the steps of positioning a probe adjacent to the surface of interest, collecting infrared light using the probe, transmitting the infrared light from the surface to analyzing means, and analyzing the light to determine one or more properties of the surface.
  • the probe preferably comprises a light collection fiber bundle comprising a plurality of collection fibers adapted to collect infrared light, each of the plurality of collection fibers having a proximal end, a distal collection end opposite the proximal end, and a conductive core located between the proximal end and the distal collection end.
  • a first balloon may be positioned on a sheath between the proximal end and the collection end of the plurality of collection fibers and a second balloon disposed on the sheath distal to the collection ends.
  • a balloon may be disposed on the probe such that the distal collection ends of the fibers lie inside the balloon.
  • Still another embodiment is directed to a method for obtaining information about a tissue surface, comprising the steps of collecting infrared radiation from the tissue surface using a probe placed proximate to the tissue surface, the probe having a longitudinal axis, transmitting the infrared radiation from the tissue surface to a remote analyzer, and analyzing the infrared information to determine properties of the tissue.
  • the remote analyzer may comprise a spectrometer and detector array.
  • preferred embodiments of the invention are directed to probes having fibers and optical coupling means uniquely suited for the collection and analysis of infrared wavelengths, as will be clear to those of skill in the art, in other embodiments, additional fibers may be incorporated into the probes, so that other wavelengths (in addition to infrared) may be collected and analyzed.
  • Figure 1 Longitudinal cross-section of a probe device according to a first embodiment of the present invention, showing an illumination fiber in phantom.
  • Figure 2 Longitudinal cross-section of a probe device according to a second embodiment of the present invention, showing a multi-fiber configuration in phantom.
  • Figure 3 Longitudinal cross-section of a probe device according to a third embodiment of the present invention.
  • Figure 4 Longitudinal cross-section of a probe device according to a fourth embodiment of the present invention. Description of the Invention
  • the present invention is directed to probe devices useful in a wide variety of medical and other procedures, including, but not limited to, endoscopic procedures such as thoracoscopy, laparoscopy, angioscopy and biopsy.
  • the present invention relates to balloon probes adapted to obtain spectroscopic information in a desirable spectral range, such as in the infrared spectral region.
  • the invention also relates to methods that utilize these probes to analyze a surface of interest, such as in connection with the diagnosis and treatment of disease.
  • the present invention overcomes the problems inherent in the use of infrared radiation in a moist environment by providing novel means for bringing the collection end of the optic fiber into unobstructed optical contact with the tissue surface.
  • Probes according to the present invention are advantageous in that they may be used to detect the composition or other qualities of a tissue surface in a non-invasive manner. For example, by detecting the frequencies and intensities of infrared light reflected or emitted from the wall, information about chemical bond energies can be obtained in a non-invasive manner. This bond energy information can then be translated into information about the composition of the wall and used as a diagnostic aid.
  • the probe devices and methods of the present invention can be used to determine tissue viability (i.e., whether tissue is dead or living, and whether it is predicted to remain living), detecting tissue ischemia (e.g., in heart, or in leg after a gunshot wound), differentiating between normal and malignant cells and tissues (e.g., delineating tumors, dysplasias and precancerous tissue, detecting metastasis), differentiating between infected and normal (but inflamed) tissue (e.g., extent of aortic root infection), quantification and identification of pathogens, and differentiating and delineating other pathologic states.
  • Applications further include evaluation of tissue and blood chemistry, as well as examining the chemistry of blood vessel walls, including lipid and plaque characteristics and determining effects of lipid-lowering agents.
  • the probes and apparatus of the present invention may also be applied by veterinarians to animals, by dentists to dental applications, such as periodontal disease, and by pathologists in connection with forensic evaluation of a tissue of interest.
  • instruments according to the invention permit a surgeon or a physician to diagnose a medical condition or develop a surgical strategy based on realtime spectroscopic information obtained during surgery or in the course of performing clinical procedures or other medical evaluations.
  • the physician is able to readily obtain significantly more information about a patient's condition than he or she might otherwise have been able to obtain. This additional information may permit a given surgical procedure to be carried out more efficiently, leading lead to more successful surgical results.
  • the general-purpose nature of instruments according to the present invention can help a surgeon develop significant amounts of medical information in time-critical surgical situations. For example, a patient may undergo surgery during which the surgeon may wish to evaluate a tumor, an area of blood vessel abnormality, or another pathological condition. Using the present invention, the physician can quickly determine the nature and extent of the pathology while the patient is still under anesthesia This is particularly beneficial during major surgery, where significantly extending surgery duration increases morbidity and mortality risk. Because the devices of the present invention allow for rapid and minimally invasive procedures, the patient's overall risk is reduced. The immediate diagnosis and evaluation possible using the devices of the present invention provide significant benefits to the patient.
  • probe or probe device 10 includes a sheath 12, an optical fiber 14, and a balloon 16.
  • Balloon 16 has a wall 17.
  • Sheath 12 is a flexible hollow tube that allows optical fiber 14 of probe 10 to be threaded along a guide wire inserted by a physician, although rigid or semi-rigid probes that do not require a guiding mechanism may also be used.
  • a needle or other suitable means may also be used to guide the probe into place.
  • Suitable optical fibers useful in the present invention include, but are not limited to infrared fibers, such as fluoride-based glasses, chalcogenide glass fibers, sulfide- based fibers and telluride-based fibers.
  • fluoride-based glass fibers are used.
  • chalcogenide glass fibers with low optical loss in the 2-11 ⁇ m wavelength region are used.
  • Another embodiment of the invention may incorporate sulfide-based fibers, which transmit in the 1 -6 ⁇ m region.
  • another embodiment may use telluride-based fibers which transmit in the 2-1 1 ⁇ m region.
  • mixtures of fibers may be used.
  • Optical fiber 14 includes a distal optical collection end 20 and a proximal optical end 26, and may include a bend 22.
  • Distal collection end 20 is responsive to a surface of tissue of a patient. Bend 22 is preferably disposed proximate to collection end 20, between collection end 20 and proximal optical end 26.
  • Proximal optical end 20 is optically coupled to spectrometer 32, such as by lens 28.
  • Spectrometer 32 is coupled to optical detector 30.
  • Spectrometer 32 is used to select one or more desired wavelengths which are transmitted to an optical detector 30 for measurement.
  • balloon 16 may be a standard angioplasty balloon designed for application to blood vessels. However, balloons of other sizes and shapes may also be employed depending on the intended application.
  • the balloon is infrared lucent or virtually infrared lucent when inflated.
  • teflon may be used to make a suitable balloon.
  • any minor opacity to infrared light may be digitally subtracted from the signal using known techniques.
  • collection end 20 of the optical fiber 14 when inserted, is disposed inside the lumen of balloon 16. Collection end 20 may directly contact the balloon wall. Alternately, there may be a gap between collection end 20 and the balloon wall 17 when the balloon is inflated.
  • probe 10 is inserted into an opening, such as an orifice or incision in a patient, and it is threaded until collection end 20 of the fiber is positioned (inside balloon 16) proximate or adjacent to the exposed tissue surface of interest.
  • Balloon 16 is then inflated, such as via an inflation channel in sheath 12 with an infrared lucent gas or liquid.
  • a preferred infrared lucent fluid is dry nitrogen gas.
  • the media or medium chosen may be determined by the specific purpose and location of the procedure.
  • collection end 20 is brought into close proximity or is optically coupled to the exposed tissue wall or surface of interest 18.
  • the optical coupling provided by the balloons of the invention allows the collection end of the probe to emit and collect infrared light unimpeded by infrared opaque fluids, such as water, blood or other bodily fluids.
  • the surface may be a lumen wall such as the wall of a blood vessel, the lining of an intestine, a chamber of the heart (e.g., to look for signs of rejection), or other appropriate lumen wall in the patient.
  • the surface to be examined can also be created by an incision, such as an incision in the breast.
  • the probes of the present invention may be used in procedures examining body cavities or any type of lumen, including fetoscopic and laparoscopic procedures.
  • Bend 22 in the fiber permits collection end 20 to collect light from a radial direction with respect to the longitudinal axis of the core of fiber 14.
  • a mirror or prism may optionally be used to collect light at an angle to the longitudinal axis of the fiber core.
  • a fiber with a straight end may be used to collect light from a direction aligned with the longitudinal axis of the fiber.
  • collection end 20 of fiber 14 is optically coupled to the tissue surface 18.
  • Light including, but not limited to, infrared radiation emitted from or reflected by the wall, is thus transmitted along fiber 14 to the spectrometer and detector by total internal reflection (TIR).
  • detector 30 is sensitive in the infrared spectral regions, allowing spectrometer 32 to present an infrared image or spectrum to the surgeon.
  • Detector 30 is preferably sensitive to wavelengths of at least 800 - 25,000 nanometers (nm) and more preferably, to wavelengths ranging from 3,000 -14,000 nm, and most preferably, to wavelengths of 6,000 - 12,000 nm.
  • the acquired spectrum may be presented directly to a physician or it may be analyzed by a computer to assist in identifying attributes of the tissue surface.
  • the light received by collection end 20 of fiber 14 may be supplied to the area of interest from source 34 through illumination fiber 36.
  • Illumination fiber 36 has a proximate end 39 optically coupled to light source 34, and a distal illumination end 41 adjacent to collection end 20.
  • the light may also be emitted from within the tissue surface itself (e.g., bioluminescence), or it may be transmitted through the tissue surface from the other side of the tissue surface.
  • fibers which are transparent in the ultraviolet region further spectral information, including information attributable to fluorescence, may be obtained.
  • a single fiber may be used to both illuminate and collect, for example, by using a beam splitter to allow both excitation and collection with a single fiber.
  • Spectrometers useful in the present invention include dispersive, fixed or tunable bandpass devices.
  • Preferred spectrometers include Fourier transform interferometers or dispersive monochromators.
  • Useful imaging spectrometers include dielectric bandpass filters and liquid crystal tunable filters (LCTFs). The spectrometer and detector may be incorporated into a single device.
  • Preferred illumination sources include infrared ceramic sources, such as a globar, or tunable infrared lasers. Other illumination sources include quartz tungsten halogen (QTH) bulbs (near infrared) and broad band visible bulbs.
  • QTH quartz tungsten halogen
  • FIG. 2 depicts a second embodiment of the present invention.
  • second probe device or probe 40 includes sheath 42, optical fiber 44, proximate balloon 46 and distal balloon 48.
  • Optical fiber 44 includes distal optical collection end 50, proximal optical end 56, and bend 52 disposed proximate to collection end 50.
  • Probe 40 differs from probe 10 in that the collection end 50 is not in apposition with or disposed inside the balloon, but instead sits between the distal and proximate balloons.
  • the collection ends of probe 40 may or may not be in apposition with tissue surface 18.
  • Sheath or conduit 42 also includes opening 65 which connects or allows communication between the inside of sheath 42 with volume 64. Volume 64 is defined by proximate balloon 46, distal balloon 48, and tissue surface 18.
  • Proximal optical end 56 of fiber 44 is functionally coupled to detector 58, such as a detector array, via a spectrometer.
  • Probe 40 may be implemented as a single-fiber or multi-fiber probe by providing one or more additional fibers 54 that run next to first fiber 44 in a bundle.
  • Fibers 54 may each include a bend 62 in a different plane causing fibers 54 to diverge radially from first fiber 44 and from each other. Alternately, the fibers may have axially offset bends 62 in the same plane.
  • Each of the fibers 54 has a distal collecting end 60 and a proximate end 66, which may be coupled to an additional detector 68 via a spectrometer.
  • the first detector 58 and the additional detector(s) 68 may form part of a detector array, such as a focal plane array (FPA).
  • the multiple fibers in this embodiment may be serviced by a single detector and an optical multiplexer.
  • FPA focal plane array
  • probe 40 is positioned in the area of interest, and distal and proximate balloons 46 and 48 are inflated. This creates cavity or enclosed volume 64 between the two balloons 46 and 48 and lumen wall 18.
  • the upstream balloon is preferably inflated first.
  • an infrared transparent coupling fluid i.e., a gas or liquid
  • Figure 3 depicts a third embodiment of the present invention.
  • probe or probe device 70 includes sheath 72, balloon 76 and fiber 74.
  • Fiber 74 has a distal collection end 77 and a proximal end 79.
  • the fiber or fibers may be, but need not be, fixed to an outer surface 73 of balloon 76.
  • Probe 70 may further include a bend 75, or a reflector that redirects light from collection end 77 into the fiber 74.
  • the fiber or fibers may be introduced separately from the balloon using a guidewire. Apposition to the wall may be accomplished by simple inflation of balloon 76.
  • probes 10, 40 and 70 may employ an autoperfusion balloon to allow antegrade blood flow during inflation.
  • the balloon may be toroidally shaped.
  • the balloon may have a passage 78 that is either centrally located or offset from the center.
  • passage 78 allows fluid communication between proximate end 71a and distal end 71b of balloon 70.
  • Probe 40 is less conducive to the addition of a passage, although a rigid sheath section may be provided that begins at the distal end of the distal balloon and ends at the proximate end of the proximal balloon.
  • Figure 4 depicts a fourth embodiment of the present invention. Referring to
  • probe or probe device 80 which may be used as an angioscope, includes collection fiber 84, illumination fiber 86, and sheath 82.
  • the two fibers 84 and 86 are arranged generally in parallel.
  • Collection fiber 84 has a collection end 90, a bend 92, and a proximal end 96.
  • Illumination fiber 86 has a distal end 100, a bend 102 and a proximate end 106.
  • the two fibers are also surrounded by a flexible sheath 82 that is preferably smaller than the diameter of the lumen of interest, and includes a bend 1 12 that generally follows bends 82 and 92 in the two fibers.
  • probe 80 may include more than one collection fiber.
  • probe 80 does not occupy the entire diameter of the lumen of interest, and therefore allows fluids such as blood to pass through the lumen while the assessment is being made.
  • this embodiment may be designed with an occlusion balloon or balloons and a perfusion lumen.
  • the embodiments described above preferably employ bends to orient the collection ends of the fibers, causing the light to be redirected by total internal reflection.
  • any other suitable means for orienting the collection ends may be substituted for these bends.
  • the means for orienting the collection of light may include mirrors, prisms or crystals to orient light collection by the fibers.
  • Different coupling methods may also be employed to couple the light to the tissue surface and to couple light from the tissue surface into the fiber, such as lenses, prisms, or waveguides.
  • an assembly made up of a looped fiber with a crystal tip at a bend in the loop is used to acquire light energy.
  • the probe may be inserted without the fiber or with the fiber retracted so that the area of the fiber with the bend lies within the sheath or analogous structure. After the probe is in position, the fiber may then be advanced out of the sheath (i.e., through a hole in the wall or an opening in the end of the sheath), causing the bend to deploy radially.
  • a probe may comprise a collection fiber having an intrinsic bend. The fiber is moveably disposed in a sheath, such that the bend deploys as the distal end of the fiber is advanced through a hole in the sheath.
  • the balloon and fluid in the balloon function as part of the total optic system.
  • the balloon is made so that it is preferably infrared lucent when inflated with infrared lucent fluid. As such, the illumination and collection of infrared light is virtually unimpeded.
  • the balloons in the embodiments of both Figures 1 and 2 also function in preventing fouling of the optic fiber(s).
  • Balloons of the present invention may have a coating on their exterior surface that contacts the tissue of interest and interacts with said tissue.
  • the balloon coating may comprise agents such as, for example, proteins, antigens, tissue stimulants, effector molecules and chemicals. The effect of contacting the tissue of interest with the balloon coating can then be analyzed according to the methods of the invention. The use of a coated balloon allows for a defined area to be impacted. Balloons of the present invention may also be useful in actively exciting or affecting a tissue of interest through effects such as changing the temperature of the tissue, or by distending, stretching or otherwise mechanically interacting with the tissue. By stretching or distending tissue, examination of tissue can be further optimized.
  • the probes of the present invention are adapted to collect and analyze infrared light and preferably process images from image planes acquired at wavelengths in the infrared region.
  • the probe devices including their detectors, may be sensitive to and capable of detecting and analyzing other spectra of light.
  • probes may alternately or additionally be sensitive to the visible and/or near infrared regions.
  • the devices may operate in multi spectral, and hyperspectral, or even ultraspectral imaging modes. ultispectral modes involve image processing derived from a relatively small number of spectral image planes (two wavelengths to about twenty wavelengths). Hyperspectral and ultra spectral imaging modes involve at least twenty image planes and can produce significantly more accurate and informative results.
  • Ultraspectral modes involve hundreds of wavelengths, and may be able to produce even further information about the surface under analysis.
  • Hyperspectral imaging may include selecting specific wavelength bands for discrimination of a particular diseased state, or it may also allow the instrument to scan for multiple conditions at the same time.
  • the probe devices of the present invention which are designed to collect and analyze specific wavelengths, have a number of potential applications. For example, wavelengths of about 550 and wavelengths of about 575 associated with oxy- and deoxy-hemoglobin may be collected and evaluated to determine blood oxygenation. The relationship between these wavelengths is described in "Hemoglobin: Molecular Genetics and Clinical Aspects,” by H. Franklin Bunn and Bernard Forget, W. B. Sanders, 1986. Another example would involve the collection and analysis of the Fourier transform infra-red spectra of the colon and rectum as described in "Human Colorectal Cancers Display Abnormal Fourier Transform Spectra," by Basil Rigas et al., Proceedings of the National Academy of Science, pp. 8140-8144, 1987.
  • the probe devices of the present invention may be designed to collect and analyze other wavelengths, depending on the intended application.
  • One embodiment of the present invention is directed to a probe device adapted to collect and analyze infrared radiation.
  • the probe device comprises a collection fiber, the collection fiber comprising a proximal end, a distal collection end opposite the proximal end adapted to collect infrared radiation, and an infrared conductive core located between the proximal end and the collection end.
  • the fiber is flexible.
  • the probe further comprises a sheath for receiving the collection fiber.
  • the fiber may be moveably disposed in the sheath.
  • the sheath surrounds at least a portion of the collection fiber during operation (i.e., during collection).
  • the probe device may further comprise a spectrometer optically coupled to the proximal end of the collection fiber and a detector, such as a detector array, functionally coupled to the spectrometer, to detect infrared radiation from the proximal end of the collection fiber.
  • a detector such as a mercury cadmium telluride (MCT) detector may be optically coupled to the spectrometer.
  • MCT mercury cadmium telluride
  • a detector element functionally coupled to the proximal end of the collection fiber may be disposed at or near the collection end of the collection fiber, and may even contact the surface of interest.
  • the instrument may further include a processing circuit functionally connected to the radiation detector.
  • the processing circuit is preferably operative to translate the level of detected radiation into a measurable signal that is indicative of the level of damage or disease in the tissue.
  • the signal may be directly evaluated, or it may be compared to stored reference profiles, to provide an indication of changes from previous levels or trends in the patient's health or disease state.
  • the probe preferably has an illumination fiber, which like the collection fiber, may be moveably disposed in the sheath.
  • the illumination fiber has a distal illumination end, which is disposed adjacent or in close proximity to the distal collection end of the collection fiber during operation, and a proximate end optically coupled to an illumination source.
  • the illumination fiber is an infrared transmitting fiber
  • the illumination source is an infrared source such as a globar.
  • the sheath preferably surrounds at least a portion of both the collection fiber and the illumination fiber during operation (i.e., during excitation and collection).
  • the collection fiber may comprise a beam splitter, which allows both excitation and collection of infrared light by a single collection fiber.
  • the probes of the present invention may alternately comprise a light source attached at the end of the probe or otherwise contained within the balloon.
  • the balloon may also serve as an optical filter for both the illumination light as well as the collected light.
  • a light source may be provided from a separate source located on one side of the tissue of interest, while the probe is located on the other side of the tissue.
  • the probe and the light source effectively create a sandwich, with the tissue of interest in the middle, thereby allowing transmitted light to be collected by the probe.
  • This sandwich embodiment also allows for volumetric analyses to be carried out on the tissue, in addition to surface assessment.
  • An optical coupler such as a curved or focusing mirror or a lens may be used to optically couple the proximal end of the collection fiber to the spectrometer.
  • the spectrometer is used to select one or more wavelengths which are transmitted to a detector, such as a detector array.
  • the collection end of the fiber is preferably adapted to collect light radiating or reflecting in a radial direction with respect to the longitudinal axis of the fiber.
  • the probe device preferably includes means proximate the collection end to orient the collection end in a radial direction with respect to a longitudinal axis of the fiber core. This may be accomplished, for example, by a bend in the fiber core.
  • Other means for orienting the collection of infrared light by the fiber, in addition to bends, include mirrors, prisms and crystals.
  • the total diameter of the collection fiber, sheath and balloon are small enough to permit them to be inserted into mammalian blood vessels.
  • the total diameter of the collection fiber, sheath and balloon may have a diameter of less than 4 mm, and more preferably, less than 2 mm when the first balloon is maximally inflated.
  • the balloons may be designed so that they can be used in the lumen of a larger organ, such as intestine.
  • the balloon or balloons may have a diameter greater than l-5cm.
  • the collection fiber may be disposed in a variety of ways with respect to the first balloon during operation of the probe.
  • the collection fiber penetrates the wall of the balloon between the collection end and the proximal end such that the distal collection end lies inside the balloon during operation.
  • the collection end of the collection fiber may be positioned adjacent to the outside of the wall of the balloon.
  • a plurality of collecting fibers may be disposed in the sheath and used to collect radiation.
  • the fibers may surround the balloon, or the collection ends may be disposed inside the balloon during operation.
  • the balloon and the liquid or gas used to inflate the balloon are preferably infrared lucent.
  • the probe device may alternately include a second anchoring balloon disposed on a portion of the sheath that extends distally past the location of the collection end of the collection fiber during operation (i.e., it extends in a direction opposite the proximal end of the probe device).
  • the first balloon is disposed on the sheath between the location of the proximal end and the location of the collection end of the collection fiber during operation
  • the second balloon is disposed on the distal portion of the sheath.
  • An opening may be disposed in the sheath between the first and the second balloons.
  • the balloons When this probe device is disposed in a lumen, the balloons may be inflated, and a fluid, preferably an infrared transparent or lucent fluid, is infused through the opening in the sheath to fill the void defined by the first and second balloons and the wall of the lumen.
  • a fluid preferably an infrared transparent or lucent fluid
  • a passage may be provided through the balloon to allow fluid communication between the proximate end and the distal end of the balloon.
  • Another embodiment of the present invention is directed to a probe device having an imaging collection fiber bundle comprising a plurality of collection fibers, each of the plurality of collection fibers comprising a proximal end, a distal collection end opposite the proximal end, and a conductive core located between the proximal end and the collection end.
  • a first anchoring balloon is disposed on the fiber bundle.
  • the probe device may further comprise a spectrometer and a detector, such as a detector array, responsive to the proximal end of the plurality of collection fibers to acquire an image.
  • the collection fibers preferably conduct infrared light, but other fibers may be used which conduct other wavelengths of light such as visible, UV and/or near infrared light.
  • the probe device may include an illumination fiber having a distal illumination end disposed adjacent the location of collection ends of the collecting fibers during operation (i.e., during excitation and collection).
  • an illumination fiber having a distal illumination end disposed adjacent the location of collection ends of the collecting fibers during operation (i.e., during excitation and collection).
  • six collection fibers may be placed circumferentially around a center illumination fiber in a hexagonal configuration, and may be oriented to efficiently collect the light.
  • a multi-fiber probe may comprise a plurality of collection fibers and a plurality of illumination or excitation fibers; in this embodiment each of the collection fibers may be associated with or disposed adjacent to its respective excitation fiber.
  • the light or data collected by each fiber may provide a single pixel of information for incorporation into an image or other display.
  • the image is preferably optimized to facilitate interpretation.
  • a two dimensional planar image may be produced from circumferential data.
  • a novel feature of balloon probes according to various embodiments of the invention relates to the incorporation of the balloon into the actual optical path.
  • the distal collection ends are disposed inside the wall of the balloon during operation.
  • This balloon is made of an infrared lucent material (or is virtually infrared lucent due to its thickness when inflated) and filled with an infrared lucent fluid to form a part of the optical path in a single fiber probe.
  • this balloon may be compartmentalized.
  • the balloon may be partitioned into a plurality of different or separate sacs or compartments.
  • the collection ends of the collection fibers are each disposed in a separate compartment.
  • the first balloon may be disposed between the location of the proximal ends and the location of the distal collection ends of the collection fibers during operation.
  • a conduit may be provided, which passes through a first anchoring balloon, and has a portion which extends distally past the location of the distal collection end of the plurality of collection fibers during operation.
  • This embodiment has a second anchoring balloon attached to the portion of the conduit that extends distally past the location of the distal collection end of the plurality of collection fibers during operation.
  • An opening may be provided in the conduit between the first and second balloons allowing fluid communication with the space between the first and second balloons.
  • the plurality of collection fibers in the fiber bundle may be positioned adjacent to the outside of the wall of the balloon, and may form a bundle that surrounds the balloon.
  • the distal collection ends of the plurality of fibers may be disposed inside the wall of the balloon during operation, and the balloon may serve as part of the coupler and collection device. In this embodiment, the collection ends are preferably close to or contact the balloon wall during operation.
  • the balloon may be partitioned into a plurality of separate compartments with the collection ends each disposed in a separate compartment.
  • the fiber bundle may be flexible, and may include means proximate the collection end of each fiber to orient the collection ends in a radial direction with respect to the axis of the core of the fibers, such as bends in the fiber cores.
  • Mirrors, prisms and crystals may also be used as a means for orienting collection of light.
  • the bends in the fiber cores orient the plurality of collection fibers in at least two different directions.
  • the detector may comprise a focal plane array such as a mercury cadmium telluride plane array or a microbolometer array.
  • the device may further comprise ah optical multiplexer such as a digital micro mirror array.
  • Instruments according to the present invention may also include imaging optic means within the probe, a spectral separator optically responsive to the imaging optic means, and an imaging sensor optically responsive to the spectral separator.
  • the spectral separator may be a tunable filter and the imaging sensor may be a two- dimensional imaging array, such as a focal plane array.
  • the instrument may optionally comprise a diagnostic processor having an image acquisition interface responsive to the imaging sensor.
  • the diagnostic processor may also have a filter control interface to which the spectral separator is responsive.
  • the diagnostic processor may also include a general-purpose processing module and diagnostic protocol modules, which may each include filter transfer functions and an image processing protocol.
  • the general-purpose processing module may be operative to instruct the filter to successively apply the filter transfer functions to light collected from the patient, to acquire from the imaging sensor a number of images of the collected light each obtained after one of the filter transfer functions is applied, and to process the acquired images according to the image processing protocol to obtain a processed display image.
  • the general-purpose processor may be a real-time processor operative to generate a processed display image within a time period on the order of the persistence of human vision. It may also be operative to acquire some images more slowly depending on the number of wavelengths and complexity of diagnostic processing protocol.
  • the sensor and filter may be operative in the visible, infra-red, and UV regions.
  • light from each fiber may be processed to generate an individual pixel for that fiber.
  • the pixels may then be arranged so that they form an image or display which can be readily interpreted or read by the user.
  • Another embodiment of the invention is directed to an endoscopic balloon probe having an infrared light source.
  • This embodiment includes a collection fiber, the collection fiber comprising a proximal end, a distal collection end opposite the proximal end adapted to collect infrared light, and a conductive core located between the proximal end and the distal collection end, an illumination fiber having a distal illumination end disposed adjacent the distal collection end of the collection fiber during operation, and a proximate end coupled to an infrared illumination source such as globar or other means to orient image collection.
  • An anchoring balloon is disposed on the probe such that the distal collection end of the collection fiber and the distal illumination end of the illumination fiber are disposed inside the balloon during operation (i.e., collection and excitation).
  • the balloon is infrared lucent.
  • a sheath may surround a portion of the collection fiber and a portion of the illumination fiber during operation.
  • the collection fiber and illumination fibers may be moveably disposed in the sheath.
  • the collection fiber may have a bend to orient the collection end in a radial direction with respect to the axis of the conductive core, or may use other means to orient image collection.
  • the present invention is also directed to novel methods for analyzing or obtaining information about the properties of a tissue or other surface of interest.
  • One such method for obtaining information about a surface of interest comprises the steps of positioning a probe adjacent to the surface of interest, collecting infrared light using the probe, transmitting the infrared light from the surface to analyzing means, and analyzing the light to determine one or more properties of the surface.
  • the probe preferably comprises a collection fiber, the collection fiber comprising a proximal end, a distal collection end opposite the proximal end adapted to collect infrared light, and an infrared conductive core located between the proximal end and the distal collection end, and a first anchoring balloon disposed on the probe.
  • the step of collecting infrared light preferably comprises collecting infrared light in the vicinity of the collection end of the probe that shines or radiates in a direction generally or substantially perpendicular to the longitudinal axis of the probe
  • the step of analyzing preferably comprises spectroscopic analysis. More preferably, the step of analyzing comprises imaging spectroscopy.
  • the distal collection end of the probe lies inside the balloon during operation, and the balloon protects the collection end of the probe from moisture and fouling.
  • the probe further comprises a sheath which surrounds a portion of the collection fiber during operation.
  • a first anchoring balloon is disposed on the sheath between the location of the proximal end and the location of the distal collection end of the collection fiber during operation.
  • the sheath has a portion that extends distally past the location of the collection end of the collection fiber during operation, and the probe further comprises a second anchoring balloon disposed on the portion of the sheath distal to the location of the collection end during operation.
  • the method may further comprise the steps of inflating the first balloon and the second balloon to create an enclosed volume defined by the first balloon, the second balloon and the lumen, and completely or partially filling the volume with a fluid, such as dry nitrogen gas.
  • a fluid such as dry nitrogen gas.
  • the balloons may be inflated sequentially to facilitate this process. For example, when the probe is inserted in a blood vessel, the upstream balloon may be inflated first, followed by the downstream balloon. The upstream balloon may be the first or the second balloon, depending on whether the probe is inserted antegrade or retrograde into the vessel.
  • the fluid used to fill the volume may be an infrared lucent gas or liquid, including optical coupling fluids such as dry nitrogen gas.
  • the distal collection end of the collection fiber is inserted into the enclosed volume after the balloons are inflated and the volume is filled with liquid.
  • Another embodiment is directed to a method for obtaining information about a surface of interest comprising the steps of positioning a probe adjacent to the surface of interest, collecting light using the probe, transmitting the light from the surface to analyzing means, and analyzing the light to determine one or more properties of the surface.
  • the probe comprises a light collection fiber bundle comprising a plurality of collection fibers adapted to collect infrared light, each of the plurality of collection fibers comprising a proximal end, a distal collection end opposite the proximal end, and a conductive core located between the proximal end and the distal collection end.
  • the probe is preferably adapted to collect infrared light.
  • the step of collecting light preferably comprises collecting light in the vicinity of the collection end of the probe that radiates or shines in a direction generally or substantially perpendicular to the longitudinal axis of the probe.
  • the step of analyzing preferably comprises spectroscopic analysis, such as imaging spectroscopy, standard or otherwise.
  • an anchoring balloon is disposed on the probe such that the distal collection ends are disposed inside the wall of the balloon during operation.
  • the probe may further comprise a sheath disposed around the fiber bundle, a first anchoring balloon disposed on the sheath between the location of the proximal ends and collection ends of the plurality of fibers during operation, and a second anchoring balloon disposed on the sheath distal to the location of the collection ends of the plurality of fibers during operation.
  • the method may further comprise the steps of inflating the first balloon and the second balloon to create an enclosed volume defined by the first balloon, the second balloon and the lumen, and emptying the volume or filling the volume with a fluid.
  • the fluid is preferably infrared lucent.
  • the distal collection ends are inserted into the enclosed volume after the balloons are inflated and the volume is filled with the fluid.
  • Another embodiment of the invention is directed to a probe in which the distal collection end of one or more collection fibers is disposed in the central hole of a toroidally-shaped anchoring balloon during operation.
  • This embodiment may optionally comprise one or more illumination or excitation fibers disposed so that the distal illumination end of the fiber or fibers are also disposed in the central hole of the balloon during operation.
  • excitation light from the distal illumination end of the illumination fiber passes through the inner wall of the balloon, the coupling fluid and the outer wall of the balloon to reach the tissue surface.
  • light coming from the tissue surface passes through the outer wall of the balloon, the coupling fluid and the inner wall of the balloon to reach the distal collection end of the probe.
  • Another embodiment of the present invention is directed to a method for obtaining information about a tissue surface, comprising the steps of collecting infrared radiation from the tissue surface using a probe placed proximate to the tissue surface, the probe having a longitudinal axis, transmitting the infrared radiation from the tissue surface to a remote analyzer, and analyzing the infrared information to determine properties of the tissue surface.
  • the step of analyzing may comprise spectroscopic analysis, such as imaging spectroscopy, standard or otherwise.
  • the step of collecting and transmitting may be performed using multiple fibers in the probe.
  • the step of collecting infrared radiation may comprise collecting infrared light in the vicinity of a collection end of the probe that radiates or shines in a direction generally or substantially perpendicular to the longitudinal axis of the probe.
  • the probe has means for optically coupling the collection end of the probe to the tissue surface.
  • Such means include all of the various balloon configurations previously described.
  • the means for optically coupling may comprise an anchoring balloon disposed around a collection end of said probe.
  • the means may comprise a first anchoring balloon and a second anchoring balloon disposed on said probe such that a collection end of said probe is positioned between said first and said second anchoring balloons.
  • the two balloons may be inflated as previously described, thereby removing or minimizing the presence of infrared opaque substances between the tissue surface and probe tip.
  • the method further comprises the step of providing a source of infrared radiation adjacent to the opposing surface of the tissue surface being analyzed, and the step of collecting comprises collecting the radiation transmitted through the tissue to the probe.
  • a source of infrared radiation adjacent to the opposing surface of the tissue surface being analyzed
  • the step of collecting comprises collecting the radiation transmitted through the tissue to the probe.

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Physics & Mathematics (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Molecular Biology (AREA)
  • Pathology (AREA)
  • Engineering & Computer Science (AREA)
  • Biomedical Technology (AREA)
  • Veterinary Medicine (AREA)
  • Medical Informatics (AREA)
  • Biophysics (AREA)
  • Surgery (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Investigating Or Analysing Materials By Optical Means (AREA)

Abstract

L'invention concerne des sondes à ballonnet conçues pour être utilisées dans l'endoscopie et d'autres procédures médicales. Lesdites sondes sont utiles pour l'obtention d'informations spectroscopiques réfléchies ou émises par un tissu à analyser, dans la zone spectrale de l'infrarouge. Les informations recueillies par la sonde sont utiles dans le diagnostic et le traitement de maladies. L'invention porte également sur des procédés dans lesquels ces sondes sont utilisées pour l'analyse d'une surface particulière, de la manière la moins invasive possible, en vue du diagnostic et du traitement d'une maladie.
PCT/US1999/020321 1998-09-03 1999-09-02 Sondes a ballonnet pour endoscope a infrarouge WO2000013578A1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AU59086/99A AU5908699A (en) 1998-09-03 1999-09-02 Infrared endoscopic balloon probes

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US9895798P 1998-09-03 1998-09-03
US60/098,957 1998-09-03

Publications (1)

Publication Number Publication Date
WO2000013578A1 true WO2000013578A1 (fr) 2000-03-16

Family

ID=22271733

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US1999/020321 WO2000013578A1 (fr) 1998-09-03 1999-09-02 Sondes a ballonnet pour endoscope a infrarouge

Country Status (2)

Country Link
AU (1) AU5908699A (fr)
WO (1) WO2000013578A1 (fr)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001001854A2 (fr) 1999-07-02 2001-01-11 Hypermed Imaging, Inc. Dispositif d'imagerie a modalite integree
EP1305768A2 (fr) * 2000-06-27 2003-05-02 Electro-Optical Sciences, Inc. Imagerie multispectrale et caracterisation de tissus biologiques internes
US6652452B1 (en) 1999-10-25 2003-11-25 Advanced Medical Electronics Corporation Infrared endoscope with sensor array at the distal tip
EP1558127A1 (fr) * 2002-11-07 2005-08-03 Infraredx, Inc. Spectroscope possedant un champ de vision modifie
EP2548606A1 (fr) * 2011-07-20 2013-01-23 Florian Netzer Cathéter pour créer une section de paroi spatialement séparée
US9274046B2 (en) 2010-04-30 2016-03-01 Chemimage Corporation System and method for gross anatomic pathology using hyperspectral imaging
US11478151B2 (en) 2011-12-14 2022-10-25 The Trustees Of The University Of Pennsylvania Fiber optic flow and oxygenation monitoring using diffuse correlation and reflectance

Citations (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4445892A (en) * 1982-05-06 1984-05-01 Laserscope, Inc. Dual balloon catheter device
US4875897A (en) * 1981-06-12 1989-10-24 Regents Of University Of California Catheter assembly
US5125404A (en) 1985-03-22 1992-06-30 Massachusetts Institute Of Technology Apparatus and method for obtaining spectrally resolved spatial images of tissue
EP0590268A1 (fr) * 1985-03-22 1994-04-06 Massachusetts Institute Of Technology Cathéter destiné à la chirurgie vasculaire par rayonnement laser
US5318024A (en) 1985-03-22 1994-06-07 Massachusetts Institute Of Technology Laser endoscope for spectroscopic imaging
US5353790A (en) 1992-01-17 1994-10-11 Board Of Regents, The University Of Texas System Method and apparatus for optical measurement of bilirubin in tissue
US5421337A (en) 1989-04-14 1995-06-06 Massachusetts Institute Of Technology Spectral diagnosis of diseased tissue
US5456252A (en) 1993-09-30 1995-10-10 Cedars-Sinai Medical Center Induced fluorescence spectroscopy blood perfusion and pH monitor and method
WO1996020638A1 (fr) * 1995-01-03 1996-07-11 Non-Invasive Technology, Inc. Coupleur optique pour un examen in vivo de tissus biologiques
US5590660A (en) 1994-03-28 1997-01-07 Xillix Technologies Corp. Apparatus and method for imaging diseased tissue using integrated autofluorescence
US5647368A (en) 1996-02-28 1997-07-15 Xillix Technologies Corp. Imaging system for detecting diseased tissue using native fluorsecence in the gastrointestinal and respiratory tract

Patent Citations (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4875897A (en) * 1981-06-12 1989-10-24 Regents Of University Of California Catheter assembly
US4445892A (en) * 1982-05-06 1984-05-01 Laserscope, Inc. Dual balloon catheter device
US5125404A (en) 1985-03-22 1992-06-30 Massachusetts Institute Of Technology Apparatus and method for obtaining spectrally resolved spatial images of tissue
EP0590268A1 (fr) * 1985-03-22 1994-04-06 Massachusetts Institute Of Technology Cathéter destiné à la chirurgie vasculaire par rayonnement laser
US5318024A (en) 1985-03-22 1994-06-07 Massachusetts Institute Of Technology Laser endoscope for spectroscopic imaging
US5421337A (en) 1989-04-14 1995-06-06 Massachusetts Institute Of Technology Spectral diagnosis of diseased tissue
US5353790A (en) 1992-01-17 1994-10-11 Board Of Regents, The University Of Texas System Method and apparatus for optical measurement of bilirubin in tissue
US5456252A (en) 1993-09-30 1995-10-10 Cedars-Sinai Medical Center Induced fluorescence spectroscopy blood perfusion and pH monitor and method
US5590660A (en) 1994-03-28 1997-01-07 Xillix Technologies Corp. Apparatus and method for imaging diseased tissue using integrated autofluorescence
WO1996020638A1 (fr) * 1995-01-03 1996-07-11 Non-Invasive Technology, Inc. Coupleur optique pour un examen in vivo de tissus biologiques
US5647368A (en) 1996-02-28 1997-07-15 Xillix Technologies Corp. Imaging system for detecting diseased tissue using native fluorsecence in the gastrointestinal and respiratory tract

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001001854A2 (fr) 1999-07-02 2001-01-11 Hypermed Imaging, Inc. Dispositif d'imagerie a modalite integree
US6652452B1 (en) 1999-10-25 2003-11-25 Advanced Medical Electronics Corporation Infrared endoscope with sensor array at the distal tip
EP1305768A2 (fr) * 2000-06-27 2003-05-02 Electro-Optical Sciences, Inc. Imagerie multispectrale et caracterisation de tissus biologiques internes
EP1305768A4 (fr) * 2000-06-27 2005-05-11 Electro Optical Sciences Inc Imagerie multispectrale et caracterisation de tissus biologiques internes
EP1558127A1 (fr) * 2002-11-07 2005-08-03 Infraredx, Inc. Spectroscope possedant un champ de vision modifie
EP1558127A4 (fr) * 2002-11-07 2008-11-26 Infraredx Inc Spectroscope possedant un champ de vision modifie
US7873406B2 (en) 2002-11-07 2011-01-18 Infraredx, Inc. Spectroscope for recovering light from re-entrant zone of arterial wall
US9274046B2 (en) 2010-04-30 2016-03-01 Chemimage Corporation System and method for gross anatomic pathology using hyperspectral imaging
EP2548606A1 (fr) * 2011-07-20 2013-01-23 Florian Netzer Cathéter pour créer une section de paroi spatialement séparée
US11478151B2 (en) 2011-12-14 2022-10-25 The Trustees Of The University Of Pennsylvania Fiber optic flow and oxygenation monitoring using diffuse correlation and reflectance

Also Published As

Publication number Publication date
AU5908699A (en) 2000-03-27

Similar Documents

Publication Publication Date Title
US8024027B2 (en) Infrared endoscopic balloon probes
US6741884B1 (en) Infrared endoscopic balloon probes
US5280788A (en) Devices and methods for optical diagnosis of tissue
US6826422B1 (en) Spectral volume microprobe arrays
AU763413B2 (en) Spectral volume microprobe arrays
JP4474050B2 (ja) マルチモード光学組織診断システム
US6870620B2 (en) Apparatus and method for determining tissue characteristics
US6110106A (en) Endoscopes and methods relating to direct viewing of a target tissue
US6507747B1 (en) Method and apparatus for concomitant structural and biochemical characterization of tissue
EP2057936B1 (fr) Procédé et système pour la caractérisation et la cartographie des lésions de tissu
EP0955863B1 (fr) Appareil pour detecter la metaplasie de barrett de l' oesophage
US20060052709A1 (en) Analysis of volume elements for tissue characterization
US20030167007A1 (en) Apparatus and method for spectroscopic examination of the colon
US20120232408A1 (en) Method and Apparatus for Cervical Cancer Screening
JPH11510254A (ja) 光学的微細プローベ及び材料のスペクトル分析方法
US11660378B2 (en) Endoscopic raman spectroscopy device
US20210244346A1 (en) Cell-collecting falloposcope and method for ovarian cancer detection
WO2000013578A1 (fr) Sondes a ballonnet pour endoscope a infrarouge
US20220330792A1 (en) Cell-collecting falloposcope and method for ovarian cancer detection
CN116763239A (zh) 宽谱荧光内窥镜装置
CA2389177C (fr) Systeme multimodal optique de diagnostic tissulaire
AU2003254731B2 (en) Spectral volume microprobe arrays

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A1

Designated state(s): AE AL AM AT AU AZ BA BB BG BR BY CA CH CN CU CZ DE DK EE ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MD MG MK MN MW MX NO NZ PL PT RO RU SD SE SG SI SK SL TJ TM TR TT UA UG UZ VN YU ZA ZW

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): GH GM KE LS MW SD SL SZ UG ZW AM AZ BY KG KZ MD RU TJ TM AT BE CH CY DE DK ES FI FR GB GR IE IT LU MC NL PT SE BF BJ CF CG CI CM GA GN GW ML MR NE SN TD TG

121 Ep: the epo has been informed by wipo that ep was designated in this application
DFPE Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101)
REG Reference to national code

Ref country code: DE

Ref legal event code: 8642

122 Ep: pct application non-entry in european phase