EP3559723A1 - Sources d'éclairement d'endoscopes à fibres multicoers - Google Patents

Sources d'éclairement d'endoscopes à fibres multicoers

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Publication number
EP3559723A1
EP3559723A1 EP17883995.7A EP17883995A EP3559723A1 EP 3559723 A1 EP3559723 A1 EP 3559723A1 EP 17883995 A EP17883995 A EP 17883995A EP 3559723 A1 EP3559723 A1 EP 3559723A1
Authority
EP
European Patent Office
Prior art keywords
endoscope
fiber
illumination
cores
imaging
Prior art date
Legal status (The legal status 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 status listed.)
Withdrawn
Application number
EP17883995.7A
Other languages
German (de)
English (en)
Other versions
EP3559723A4 (fr
Inventor
Asaf SHAHMOON
Zeev Zalevsky
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Zsquare Ltd
Original Assignee
Z Square Ltd
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
Priority claimed from US15/387,805 external-priority patent/US10398294B2/en
Application filed by Z Square Ltd filed Critical Z Square Ltd
Publication of EP3559723A1 publication Critical patent/EP3559723A1/fr
Publication of EP3559723A4 publication Critical patent/EP3559723A4/fr
Withdrawn legal-status Critical Current

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Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B1/00—Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor
    • A61B1/00163—Optical arrangements
    • A61B1/00165—Optical arrangements with light-conductive means, e.g. fibre optics
    • A61B1/00167—Details of optical fibre bundles, e.g. shape or fibre distribution
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B1/00—Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor
    • A61B1/00002—Operational features of endoscopes
    • A61B1/00004—Operational features of endoscopes characterised by electronic signal processing
    • A61B1/00006—Operational features of endoscopes characterised by electronic signal processing of control signals
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B1/00—Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor
    • A61B1/00002—Operational features of endoscopes
    • A61B1/00004—Operational features of endoscopes characterised by electronic signal processing
    • A61B1/00009—Operational features of endoscopes characterised by electronic signal processing of image signals during a use of endoscope
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B1/00—Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor
    • A61B1/00163—Optical arrangements
    • A61B1/00172—Optical arrangements with means for scanning
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B1/00—Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor
    • A61B1/00163—Optical arrangements
    • A61B1/00194—Optical arrangements adapted for three-dimensional imaging
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B1/00—Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor
    • A61B1/06—Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor with illuminating arrangements
    • A61B1/063—Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor with illuminating arrangements for monochromatic or narrow-band illumination
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B1/00—Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor
    • A61B1/06—Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor with illuminating arrangements
    • A61B1/0638—Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor with illuminating arrangements providing two or more wavelengths
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B1/00—Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor
    • A61B1/06—Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor with illuminating arrangements
    • A61B1/0655—Control therefor
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B1/00—Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor
    • A61B1/06—Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor with illuminating arrangements
    • A61B1/07—Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor with illuminating arrangements using light-conductive means, e.g. optical fibres
    • G—PHYSICS
    • G02—OPTICS
    • G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B23/00—Telescopes, e.g. binoculars; Periscopes; Instruments for viewing the inside of hollow bodies; Viewfinders; Optical aiming or sighting devices
    • G02B23/24—Instruments or systems for viewing the inside of hollow bodies, e.g. fibrescopes
    • G02B23/2407—Optical details
    • G02B23/2423—Optical details of the distal end
    • G—PHYSICS
    • G02—OPTICS
    • G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B23/00—Telescopes, e.g. binoculars; Periscopes; Instruments for viewing the inside of hollow bodies; Viewfinders; Optical aiming or sighting devices
    • G02B23/24—Instruments or systems for viewing the inside of hollow bodies, e.g. fibrescopes
    • G02B23/2407—Optical details
    • G02B23/2461—Illumination
    • G02B23/2469—Illumination using optical fibres
    • G—PHYSICS
    • G02—OPTICS
    • G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B23/00—Telescopes, e.g. binoculars; Periscopes; Instruments for viewing the inside of hollow bodies; Viewfinders; Optical aiming or sighting devices
    • G02B23/24—Instruments or systems for viewing the inside of hollow bodies, e.g. fibrescopes
    • G02B23/26—Instruments or systems for viewing the inside of hollow bodies, e.g. fibrescopes using light guides
    • G—PHYSICS
    • G02—OPTICS
    • G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B27/00—Optical systems or apparatus not provided for by any of the groups G02B1/00 - G02B26/00, G02B30/00
    • G02B27/48—Laser speckle optics
    • G—PHYSICS
    • G02—OPTICS
    • G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B6/00—Light guides; Structural details of arrangements comprising light guides and other optical elements, e.g. couplings
    • G02B6/02—Optical fibres with cladding with or without a coating
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B1/00—Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor
    • A61B1/00064—Constructional details of the endoscope body
    • A61B1/00071—Insertion part of the endoscope body
    • A61B1/0008—Insertion part of the endoscope body characterised by distal tip features
    • A61B1/00094—Suction openings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B1/00—Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor
    • A61B1/12—Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor with cooling or rinsing arrangements
    • A61B1/127—Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor with cooling or rinsing arrangements with means for preventing fogging
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B1/00—Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor
    • A61B1/12—Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor with cooling or rinsing arrangements
    • A61B1/128—Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor with cooling or rinsing arrangements provided with means for regulating temperature
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61N—ELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
    • A61N5/00—Radiation therapy
    • A61N5/06—Radiation therapy using light
    • A61N2005/063—Radiation therapy using light comprising light transmitting means, e.g. optical fibres
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61N—ELECTROTHERAPY; MAGNETOTHERAPY; RADIATION THERAPY; ULTRASOUND THERAPY
    • A61N5/00—Radiation therapy
    • A61N5/06—Radiation therapy using light
    • A61N5/0601—Apparatus for use inside the body

Definitions

  • the present invention relates to the field of endoscopy, and more particularly, to multicore fiber endoscopes.
  • Endoscopes in various configurations allow efficient treatment of a range of medical problems, as well as means for manipulating different situations with limited access. Endoscope operations are challenging in that illumination, detection and treatment are confined to long and narrow operations modes. Fiber optics technology is a central enabler for such techniques, and fiber-based endoscope experience continuous improvements.
  • One aspect of the present invention provides an endoscope having a distal tip and a proximal tip, the endoscope comprising at least one multicore fiber module comprising at least one hundred cores distributed at a fill factor smaller than 1/4, an illumination source coupled to the at least one multicore fiber module and configured to deliver illumination thereto, at least one optical element, in optical communication with the cores, at the distal tip, a detector, in optical communication with the cores, at the proximal tip, and a processor configured to receive images from the detector; wherein the endoscope is configured to implement super-resolved imaging by micro scanning over a pitch distance between the cores, and wherein the endoscope is configured to implement three dimensional sensing by handling the cores group-wise with respect to radiation delivered therethrough, and to at least one of: enhance, by configuring the at least one optical element, a field of view of the endoscope beyond a region facing the cores at the distal tip, and enhance, by configuring the at least one optical element, a depth
  • Figures 1A-1E are high level schematic illustrations of endoscope configurations according to some embodiments of the invention.
  • Figures 2A-2C are high level schematic illustrations of fiber cross sections having a large number of cores in their electromagnetic propagation region(s), according to some embodiments of the invention.
  • FIGS 2D and 2E are high level schematic illustrations of fiber production by packing fiber modules, according to some embodiments of the invention.
  • Figures 3A-3C are high level schematic cross section illustrations of fibers having working channels and additional channel positions for treatment or illumination fibers, according to some embodiments of the invention.
  • Figure 3D is a high level schematic illustration of a fiber with an assembled front lens, according to some embodiments of the invention.
  • FIGS 3E-3G are high level schematic illustrations of a defogging mechanism and its effects, according to some embodiments of the invention.
  • Figures 4A-4D are high level schematic illustrations of hollow endoscope fibers having optical elements at the distal tip which compensate for the central void, according to some embodiments of the invention.
  • Figures 5A-5C are high level schematic illustrations of optical elements, according to some embodiments of the invention.
  • Figures 6A and 6B are high level schematic illustration of fiber cross sections with different configurations of the cores, according to some embodiments of the invention.
  • Figure 6C illustrates comparative experimental results of full core and hollow core fibers, according to some embodiments of the invention.
  • Figure 7 is a high level schematic flowchart illustrating a method, according to some embodiments of the invention.
  • Figures 8A-8E are high level schematic illustrations of experimental imaging results for bundled fibers, according to some embodiments of the invention.
  • Figures 9A-9D are images that provide examples for performance of the endoscope, according to some embodiments of the invention.
  • distal and proximal refer to the ends of the endoscope.
  • the end and associated parts of the endoscope which are far from the endoscope's interface (detector or eye) and close to the imaged tissue and to its surroundings is termed the distal end, while the end and associated parts of the endoscope which are close to the endoscope's interface and are remote from the imaged tissue, being typically outside the body is termed the proximal end.
  • reflected as used in this application refers to a change in a direction of an illumination wavefront which impacts one or more imaged object or tissue.
  • reflection is understood broadly as any radiation gathered by the fiber, irrespective of the source of the illumination which is reflected by the object(s) and/or tissue(s).
  • near field imaging refers to the formation of an image (of imaged objects, tissues and/or their surroundings) at the distal end of the endoscope fiber, typically at the fiber's tip. The imaged is then typically transferred through the fiber to the detector, possibly through proximal optical elements.
  • near field imaging may relate to different types of optical systems, including direct imaging without any optical elements between the imaged object or tissue and the fiber tip as well as to imaging through optical element(s) such as lenses.
  • far field imaging refers to the formation of a Fourier transform of imaged objects, tissues and/or their surroundings at the distal end of the endoscope fiber (e.g., the distal end of the endoscope fiber is at the aperture or pupil plane of the optical system), typically at the fiber's tip.
  • the image of the imaged objects, tissues and/or their surroundings may be formed at the proximal end of the endoscope fiber, typically at the fiber' s proximal tip or directly on the detector, possibly through proximal optical elements.
  • far field imaging may relate to different types of optical systems.
  • far field imaging may be direct in the sense that no optical elements are used between the imaged object or tissue and the distal fiber tip, which delivers radiation entering the fiber along the fiber to the detector at the proximal end of the fiber.
  • far field imaging may be carried out with optical elements positioned between the imaged object or tissue and the distal fiber tip, with the distal fiber tip being at least approximately at the Fourier plane (also termed aperture plane and pupil plane in different contexts) of the optical elements.
  • the fibers may have hundreds or thousands of cores and possibly incorporate working channel(s) and additional fibers.
  • the fiber may be used at different optical configurations to capture images of tissue and objects at the distal tip and to enhance a wide range of optical characteristics of the images such as resolution, field of view, depth of field, wavelength ranges etc.
  • Near-field imaging as well as far-field imaging may be implemented in the endoscopes and the respective optical features may be utilized to optimize imaging.
  • Optical elements may be used at the distal fiber tip, or the distal fiber tip may be lens-less. Diagnostics and optical treatment feedback loops may be implemented and illumination may be adapted to yield full color images, depth estimation, enhanced field of view and/or depth of field and additional diagnostic data, as disclosed below.
  • multicore endoscope fibers are disclosed.
  • the described embodiments are roughly and not exclusively described in groups relating to the following traits.
  • Certain endoscope embodiments may implement far field imaging (see Figure 1A below), e.g., have the image formed at the proximal end of the endoscope fiber, while certain endoscope embodiments may implement near field imaging (see Figure IB below), e.g., have the image formed at the distal end of the endoscope fiber.
  • Both far field and near field implementations may have distal optical elements between the imaged objects or tissues and the distal fiber tip (see Figure 1C below), or may operate without such distal optical elements (see Figure ID below).
  • each of the four combinations has different features, advantages and disadvantages as exemplified in Table 1, and may be selected according to specific implementation scenarios. Alternation of the combination may be carried out between applications or in real time, to combine advantages of different configuration types. It is further noted that endoscopes may be designed to have several combinations, e.g., a part of the fiber face (or certain fiber modules) having distal optics for imaging far objects and another part of the fiber face (or other fiber modules) lacking distal optics for microscopic imaging.
  • Certain embodiments comprise lens-less embodiments in which the distal fiber tip lacks optical elements.
  • Lens-less embodiments may implement either far-field or near- field imaging, and may utilize structural features to enhance optical resolution, apply super-resolution methods and retrieve wavefront information while reducing crosstalk between the cores.
  • Endoscope embodiments may have full tip cross sections or have working channel(s) within the imaging fiber characterized by different configurations and uses, integrating additional fibers etc., in which case the cores and optical elements may be configured to overcome the reduction of the field of view due to the incorporation of the working channel.
  • the disclosed endoscopes may serve different purposes, e.g., may be designed as a laparoscope or an ureteroscope. It is noted that elements disclosed in the context of some of the embodiments are not necessarily limited to these embodiments but may be implemented within other embodiments as well.
  • FIGS 1A-1E are high level schematic illustrations of endoscope configurations according to some embodiments of the invention.
  • Proposed micro endoscope 105 is constructed from large plurality of cores (e.g.. one hundred cores or more, hundreds of cores, thousands of cores, in certain embodiments tens or hundreds of thousand cores per fiber or fiber module, reaching over a million cores in certain fiber endoscopes), each responsible for transferring a single or a large number of spatial degrees of freedom out of which at the output, proximal end (the one external to the patient body), a high resolution color image may be constructed.
  • cores e.g.. one hundred cores or more, hundreds of cores, thousands of cores, in certain embodiments tens or hundreds of thousand cores per fiber or fiber module, reaching over a million cores in certain fiber endoscopes
  • a high resolution color image may be constructed.
  • Multi-core fiber 100 exhibits a high degree of flexibility in its optical design, as exemplified below, which may be utilized and adapted for specific applications, for example for ureteroscopes with a large working channel and a small external diameter or for laparoscopes with a very high resolution obtained at a small external diameter.
  • Endoscope 105 may be configured to carry out far-field imaging, near-field imaging or a combination of far-field imaging and near-field imaging. Irrespectively of the imaging mode, endoscope 105 may be configured to have one or more optical elements 140 at a distal tip 101 of fiber 100 or have no optical elements between tip 101 and imaged tissue(s) or object(s) 70. Certain embodiments may comprise removable or reconfigurable optical elements 140 at tip 101 and/or optical elements 140 affecting only parts of the surface of distal tip 101 (e.g., sub-group(s) of the cores).
  • Certain embodiments comprise endoscopes 105 having a plurality of fibers 100, grouped together, each having at least one hundred cores distributed at a fill factor smaller than 1 ⁇ 4, or even smaller than 1/9, at least one photonic illumination fiber, and at least one optical element at a distal tip of fibers 100, which may be configured to enhance a field of view and/or a depth of field of endoscope 105 beyond a region facing a tip of fibers 100 and congruent thereto (see details below).
  • Endoscope 105 may be further configured to implement three dimensional sensing by handling the cores group-wise with respect to radiation delivered therethrough (see details below).
  • Endoscope 105 may be further configured to super-resolved imaging by micro scanning over a pitch distance between the cores (see details below).
  • Endoscope 105 may be configured to comprise a LED (light emitting diode) light source located at distal tip 101 as the illumination source.
  • LED light emitting diode
  • FIG. 1A schematically illustrates far-field imaging, in which an image 73 (indicating any kind of electromagnetic signal reflected from tissue or object 70) is delivered through tip 101 and fiber 100 to yield image 75 on detector 91.
  • Tip 101 may be a Fourier plane (also termed aperture plane or pupil plane) at which the Fourier transform 74 of image 73 enters fiber 100. It is noted that the Fourier plane may be located anywhere along fiber 100 as well as distally or proximally to fiber 100, in different embodiments of the invention, and be optically transformed to image 75 on detector 91. Alternatively or complementary, Fourier image 74 or derivatives thereof may be measured at detector 91, and/or manipulated to enhance imaging parameters such as resolution, field of view and depth of focus, as non-limiting examples. Optical elements may be introduced distally or proximally to fiber 100 to modify or manipulate the radiation entering tip 101 and the radiation falling on detector 91, respectively.
  • Figure IB schematically illustrates near-field imaging, in which image 73 yields image 75 at fiber tip 101.
  • Image 75 is then delivered, possibly through optical elements, to detector 91 through fiber 100. It is noted that image 75 may be formed within fiber 100 and not necessarily exactly at tip 101. Image 75 delivered via fiber 100 may be measured at detector 91, and/or manipulated to enhance imaging parameters such as resolution, field of view and depth of focus, as non-limiting examples.
  • Optical elements may be introduced distally or proximally to fiber 100 to modify or manipulate the radiation entering tip 101 and the radiation falling on detector 91, respectively.
  • Figure 1C schematically illustrates optical configurations having one or more optical element(s) 140 at the distal end of fiber 100, at proximity to imaged tissue 70.
  • Optical element(s) 140 may be attached to tip 101 or may be somewhat distally removed from tip 101 (e.g., held by spacers at a distance therefrom).
  • Each optical element 140 may be in optical communication with a respective core or a respective group of cores.
  • illumination 85 is delivered to fiber 100 by an illumination source 160, and reflected illumination (e.g., in far-field, in near-field or in an intermediate plane) is directed from the cores to a detector 91, e.g., via a beam splitter 90.
  • Proximal optical elements may be set and used to manipulate illumination 85 and the reflected illumination, as symbolized below ( Figure ID) by lenses 84, 94 respectively.
  • One or more processor(s) 170 may be configured to control the illumination and/or process the detected illumination, as well as control illumination and image beams in case there are controllable elements in the optical path.
  • Figure ID schematically illustrates optical configurations having no optical element(s) (also termed below “lens-less” configurations) at the distal end of fiber 100, so that fiber tip 101 is used directly to deliver and receive illumination to and from imaged tissue 70.
  • Illumination 85 is delivered to fiber 100 proximally, e.g., via an optical element 84 such as a lens, and reflected illumination is directed to detector 91 via another optical element 94, e.g., a lens.
  • One or more processor(s) 170 may be configured to control the illumination and/or process the detected illumination, as well as control illumination and image beams in case there are controllable elements in the optical path.
  • lens-less configurations may be configured to generate image at "contact mode", e.g., with close proximity of the fiber tip to the examined tissue, to yield microscopic resolution determined by the sizes of the cores.
  • proximal optical elements 94 may be variable and be used to adjust the plane and depth of focus of captured images in far-field imaging configurations, especially in lens-less configurations.
  • Figure IE is a high level schematic block diagram illustrating endoscope configurations according to some embodiments of the invention. Various embodiments are illustrated, which may be stand-alone embodiments or be implemented in any combination thereof. In particular, various embodiments of illumination source 160 and of configurations of processor 170 are presented, which may be used to improve the spatial resolution, in particular when using super resolution algorithms, improve the beam quality and/or enhance the functionality of endoscope 105 with respect to its medical uses and image quality. Embodiments illustrated in Figure IE may be applied to any embodiment of endoscope 105 described herein. It is noted that illumination source 160 may be configured to deliver illumination 85 through one or more dedicated illumination fiber(s) 102 and/or through multicore fiber 100.
  • illumination fiber(s) 102 may be multimode fiber(s), possibly made of glass fiber, which are associated with multicore fiber 100, e.g., attached thereto or positioned in a cavity in multicore fiber 100.
  • illumination fiber(s) 102 may be positioned to illuminate tissue 70 in any other spatial relation to multicore fiber 100, possibly in no mechanical association therewith.
  • one or more of illumination fiber(s) 102 may be single mode fibers. It is noted that the spatial relation between illumination fiber(s) 102 and multicore fiber 100 may be configured to have multicore fiber 100 receive radiation (illuminated by illumination fiber(s) 102) which is reflected off tissue 70 and/or transmitted through tissue 70, depending on specific use conditions.
  • illumination source 160 may comprise a coherence modulator 162 configured to enable processor 170 to implement algorithms for improving super resolution results 172.
  • coherence modulator 162 may be configured to use a coherence modulation of illumination 85 that reduces speckle patterns by modulating the coherence using Barker codes rather than random prior art modulation.
  • using Barker codes may reduce the required number of modulation steps for a given reduction of speckle patterns due to the orthogonality between the Barker codes and other characteristics of their definition. Specific Barker codes may be selected to optimize their application.
  • illumination source 160 may comprise multiple narrowband wavelengths 62 (e.g., narrowband spectral ranges around specified wavelengths) which may be used in processors 170 configured to provide diagnostics using one or more wavelength combinations 174, discussed below in more detail, and/or configured to implement wavelength multiplexing super resolution 176 by changing the ratios between specific wavelengths (e.g., between narrowband red, green and blue sources 62) - to achieve improved super resolution results 180.
  • narrowband wavelengths 62 e.g., narrowband spectral ranges around specified wavelengths
  • processors 170 configured to provide diagnostics using one or more wavelength combinations 174, discussed below in more detail, and/or configured to implement wavelength multiplexing super resolution 176 by changing the ratios between specific wavelengths (e.g., between narrowband red, green and blue sources 62) - to achieve improved super resolution results 180.
  • illumination source 160 may comprise one or more photonic crystal fiber (PCF) 164 configured to deliver wideband white spectrum 177 into dedicated illumination fiber(s) 120 and/or multicore fiber 100, e.g., utilizing supercontinuum effects (bandwidth broadening due to nonlinear effects) to provide white illumination of tissues that is closer to natural wideband illumination than illumination with narrowband red, green and blue sources 62 which are delivered to PCF 164.
  • PCF 164 may be coupled to one or more narrowband sources 62 and designed to have zero dispersion point(s) at the wavelengths of source(s) 62 to yield spectral broadening.
  • Using several multiple narrowband wavelengths 62 may provide wideband white spectrum 177 through a combination and merging of the broadened spectra of source(s) 62.
  • Improved white spectrum 177 may be advantageous to provide truer imaging colors be endoscope 105.
  • illumination source 160 may comprise structured light patterned illumination 168, which may be used in processor 170 configured to provide 3D sensing 178 by analyzing the illuminated patterns on the tissue and/or improved super resolution results 180 by utilizing the parameters of the temporally changing spatially projected patterns of illumination 168 to implement temporal multiplexing super resolution 179.
  • illumination source 160 may comprise one or more laser source(s) 64 (possibly narrowband sources 62) in illumination source 160 and at least one beam shaping element 182 at the distal end of multicore fiber 100 which is configured to generate an optimized beam profile 184 to improve illumination 85.
  • beam profile 184 may comprise a uniform illumination distribution in space or a rectangular uniform profile (top hat illumination distribution), which are advantageous with respect to prior art Gaussian illumination distribution with respect to various parameters of the resulting images.
  • the coherence of laser source(s) 64 may be used to shape illumination beam 85 efficiently by beam shaping element 182.
  • at least one beam shaping element 182 may be set at the proximal end of multicore fiber 100.
  • illumination source 160 may comprise one or more laser treatment source(s) 66 which are configured to apply a specified treatment 67 by endoscope 105, e.g., to a tissue.
  • treatment 67 may be applied to kidney stones in endoscope 105 designed as an ureteroscope, as described below in more details.
  • FIGS 2A-2C are high level schematic illustrations of fiber cross sections having a large number of cores 115 in their electromagnetic propagation region(s) 110, according to some embodiments of the invention.
  • Fiber(s) 100 may comprise central or eccentric optical cores (110) and/or may have hollow, central or eccentric region(s) (112) that may be used for treatment such as energy delivery, suction, illumination, drug delivery etc.
  • Illumination means (such as dedicated illumination fiber(s) 102), may be integrated in various ways within the multicore fibers 100.
  • Fiber 100 illustrated in Figure 2A may have any form of cross section, e.g., square as illustrated in a non-limiting manner, round, hexagonal, elliptic etc.
  • Figure 2A illustrates a solid cross section of fiber 100
  • Figure 2B illustrates hollow endoscope having a void 112 within fiber 100 that may be used for different purposes as disclosed below (e.g., as a working channel for inserting a tool or carrying out suction, for incorporating additional fibers etc.).
  • Fibers 100 may be square, round or have any other form, and void 112 may too have any shape and any position within fiber 100, void(s) 112 and fiber 100 may have any dimensions (Ri, R 0 , D, W etc.), and voids may also be multiple (e.g., fiber 100 may enclose two or more voids), all designed according to requirements from the endoscope.
  • Figure 2C schematically illustrates multicore fiber 100 with cores 115 grouped into "super core" groups 116 that may be configured to sense wavefronts in lens-less configurations, as explained below.
  • Multicore fiber 100 may be made of biocompatible materials in case of medical uses, e.g., polymers such as PMMA (poly-methyl methacrylate) and PS (polystyrene) and may be flexible. Fiber 100 may also be made of non-compatible materials and be flexible or rigid in case of industrial uses. Fiber 100 may be configured to have a flexibility characterized by a Young's modulus smaller than 10 GPa and to be disposable. Fiber 100 may thus be more flexible than glass fiber (having a Young's modulus of about 65 GPa), and may reach PMMA flexibility (Young's modulus between 1.8 and 3.1 GPa) or higher flexibility.
  • PMMA poly-methyl methacrylate
  • PS polystyrene
  • Fiber 100 may be configured to have a flexibility characterized by a Young's modulus smaller than 10 GPa and to be disposable. Fiber 100 may thus be more flexible than glass fiber (having a Young's modulus of about 65 GPa), and may reach PMMA flexibility (Young's modul
  • Various embodiments compensate for the reduced transparency of polymer fibers with respect to glass fibers, using means such as fiber materials, configuration of cores and interspaces, number and sizes of cores, material modifications of different fiber parts, control over the number of propagation modes in cores 115, optical means such as lenses or prisms at either side of fiber 100 and their configuration, design and application of different types of illumination and algorithmic solutions, all of which are exemplified below in a non-limiting manner.
  • the following disclosure also addresses ways to control cross talk between cores 115 (e.g., interaction effects between radiation propagating in adjacent cores 115) and ways to improve the information content and to enhance treatment-relevant information of the detected images.
  • Illumination may comprise coherent light or incoherent light, any spectral pattern (broad or narrow wavelength ranges, continuous or discrete ranged), polarized (in various patterns) or non-polarized light and different ranges in the visual or infrared ranges.
  • Material differences between cores, interspaces and outer cladding may comprise different materials, using air cores or air interspaces, and doping any of the fiber regions to influence their refractive indices, as explained in more details below. It is noted that any of the embodiments presented below may be used in any of the other embodiments described herein, as long as they are compatible. Particularly, computational methods optical methods and fiber design considerations described in the context of any embodiment may be applied to other embodiments as well.
  • Multi-core fibers 100 may be produced using fiber modules or units 117.
  • Each fiber module 117 is itself a multicore fiber, possibly configured to have uniform dimensions.
  • Such embodiments are referred to as bundled fibers, and may bundle any number of fiber modules 117 in any configuration (e.g., 2x2 modules, 3x3 modules etc.).
  • Fiber module 117 may have any form, such as square, rectangular, round or elliptic, and may be packed into fibers 100 having a wide range of forms and configurations, Introducing fiber modules 117 having an intermediate dimension between cores or core groups and whole fiber 100 (each module 117 may have e.g.
  • rectangular fiber 100 may be assembled from rectangularly arranged square fiber modules 117, e.g., using a package support 118A and a respective attachable cover 118B. Fiber modules 117 may simply be mechanically held by package support 118A and cover 118B at certain regions along fiber 100 and/or fiber modules 117 may be glued together or otherwise attached at least at certain regions.
  • fiber modules 117A, 117B may be arranged around void 112.
  • fiber modules 117A, 117B may be arranged to differ in their observation angles and/or in optical elements 140 attached at fiber tip 110 (see e.g., below, Figures 4A-4D).
  • fiber units 117A may be configured to cover a field of view in front of void 112 (e.g., be inclined inwards or have respective optical elements) while fiber units 117B may be configured to cover a field of view laterally beyond tip 101 (e.g., be inclined outwards or have respective optical elements).
  • non-limiting inclination angles may be 5-20° inwards and 10-50° outwards.
  • Respective packaging or attachment configurations may be applied to fixate fiber modules 117A, 117B in their respective positions and angles.
  • the annular arrangement of fiber modules 117A, 117B may be at the fiber's distal end, while fiber modules 117A, 117B may be separated and re-arranged differently at the fiber's proximal end, e.g., into a rectangular form to cover a face of a single rectangular detector.
  • FIGS 3A-3C are high level schematic cross section illustrations of fiber 100 having working channel 112 and channel positions 120 for treatment or illumination fibers 102, according to some embodiments of the invention.
  • Working channel 112 depicted as void 112 within fiber 100, is surrounded by electromagnetic propagation multicore fiber region 110.
  • Treatment and/or illumination fiber(s) 102 may be integrated into fiber 100 of the endoscope in a way that allows combined imaging and treatment using one fiber, immediate image feedback of the treatment etc. Such combination may be used e.g., as ureteroscope or as any other type of endoscope.
  • positioning additional fibers in channels 120 near working channel 112 may be configured to cool down the fibers (e.g., treatment fibers) by the liquids flowing through working channel 112.
  • treatment or illumination fibers 102 may be inserted at indicated positions 120 (e.g., grooves, or channels), e.g., at an inner wall of multi-core imaging region 110 in fluid communication with working channel 112, e.g., on the periphery of voids 112 ( Figure 3A, channel diameter e.g., ca. 250 ⁇ ), at an outer wall of multi-core imaging region 110 in fluid communication with the surroundings of fiber 100, e.g., on the periphery of fiber 100 ( Figure 3B, channel diameter e.g., ca. 250 ⁇ ), within multi-core imaging region 110 ( Figure 3C, channel diameter e.g., ca. 200 ⁇ ), or combinations of these possibilities. Integration of the treatment or illumination fibers 102 may be carried out before, during or after production of fiber 100. In certain embodiments, glass treatment or illumination fibers 102 may be inserted into grooves 120 after pulling polymer fiber 100.
  • Figure 3A channel diameter e.g., ca. 250 ⁇
  • Figure 3B channel diameter e.g.
  • treatment or illumination fibers may be configured and controlled to operate collectively, simultaneously or sequentially, to achieve a desired illumination and/or treatment.
  • the treatment channel may be split into several low power channels 120 to have thinner channels and lower power delivery through each channel.
  • Such configuration may enable increasing the mechanical flexibility of the endoscope, which is very important, e.g., in the field of ureteroscopy.
  • the usage of hollow channels 120 for inserting the external illumination or treatment fibers provides a device configuration exhibiting self-alignment.
  • Figure 3D is a high level schematic illustration of fiber 100 with an assembled lens 119, according to some embodiments of the invention.
  • a modular construction of fiber 100 may be used to modify some of fiber modules 117 to incorporate features into fiber 100 in a simpler manner than incorporating these features into a uniform fiber, fiber modules 117D may be configured in a modular, building block style manner to form various cross sectional organizations with respect to form and functionality of the endoscope.
  • two non-adjacent fiber modules 117D may be coated with a conductor (e.g., a metal) while the rest of fiber modules 117C may be uncoated (and insulating).
  • Such configurations may be used to deliver electricity to fiber tip 101.
  • electromagnetic signals or electromagnetic radiation may be delivered via fiber modules 117D to adjacent tissues or to associated devices or components (e.g., checking equipment or endoscope instrumentation).
  • electromagnetic energy may be delivered to distal lens 119 for heating it to prevent fogging upon entry to the body.
  • an antenna structure (not shown) may be designed upon lens 119, which receives electromagnetic radiation to heat lens 119 without using contacts.
  • radiofrequency (RF) treatment may be applied to tissue or objects surrounding fiber tip 101 via the conductive coating of fiber modules 117D.
  • Figures 3E-3F are additional high level schematic illustrations of a defogging mechanism 121 and its effects, according to some embodiments of the invention.
  • Figure 3E illustrates lens 119 coated by a conductive coating 122 connected to an electric circuit 123 configured to heat lens 119 via coating 122, to prevent fog and to defog lens 119 when required.
  • Figure 3F exemplifies image deterioration by fog accumulation - the top image (A) taken a short time after the beginning of fog accumulation, the bottom image (B) taken later, with the object, marked by an arrow, barely visible.
  • Figure 3G illustrates the image after defogging - both object and illumination spot are clear again.
  • endoscope 105 may be designed to be very thin (e.g., 0.5mm in diameter) while providing high resolution images, and distal lens 119 may also be ultra- thin.
  • the disclosed defogging mechanism provides effective control of the temperature of lens 119 using a small amount of electrical power, to prevent fogging and overcome an important prior art limitation.
  • endoscope 105 may be operated in the far field ( Figure 1A) or in the near field ( Figure IB) by properly adapting the focal length of the external optics (the one outside the patient's body, e.g., optical elements 84, 94) to the working distance of treated tissue 70 from the distal tip of the endoscope.
  • Fiber 100 may be configured to deliver full images even with working channel 112 in the middle of the imaging surface by employing far field imaging, e.g., using imaging lens 94 adapted to have a central blocked aperture.
  • obtained images may have a number of pixels that is not related to the number of cores 115, enhancing the image resolution with respect to near field embodiments.
  • certain embodiments comprise using as detector 91 an integral imaging sensor capable of sensing wavefront or the 3D topography of inspected tissue 70.
  • cores 115 may be configured to have a small number of possible spatial modes, resembling the Shack-Hartmann interferometer or a wavefront sensor.
  • cores 115 may be grouped into "super-cores" 116 (see Figure 2C), each comprising a group of adjacent cores 115.
  • Each "super-core” 116 may be handled as a single wavefront sensing element which delivers information about the wavefront by comparing radiation propagating through individual core members 115 within each "super-core” 116 (or light field sensing, e.g., comparing light directions at different cores operating in near field and multi-mode).
  • the grouping of cores 115 into “super-cores” 116 may be uniform across the face of fiber 100 or be variable, some core groups being larger than others, see e.g., the larger central core group in Figure 2C).
  • the grouping of cores 115 may be changed in time according to imaging performance preferences, based e.g., on an even (or uneven) distribution of cores 115 across fiber 110. It is noted that in such configurations a tradeoff exists between depth measurements and resolution. A larger number of cores 115 in each "super-core" 116 provides more details about the three dimensional structure of the imaged region by using more detailed wavefronts, while smaller numbers of cores 115 per group 116 and no grouping at all provide higher resolution. The grouping of cores 115 may hence be designed or modified according to spatially and temporally changing imaging requirements.
  • cores 115 may be handled by processor 170 group-wise with respect to the radiation delivered therethrough, to implement each group 116 as a wavefront sensor.
  • the allocation of cores 115 to core groups 116 may be carried out dynamically, e.g., by processor 170. Additionally, grouping considerations may accompany other considerations regarding imaging performance such as suggested techniques for enhancing resolution and/or depth measurements.
  • near field implementations may comprise sensing the light field between the cores (operating in multi-mode), e.g., measuring directional components of the radiation to yield 3D imaging.
  • Light field sensing may be carried out groupwise with respect to the core grouping.
  • endoscope fiber 100 may comprise multiple cores 115 that are not positioned at equal distances but interspaced unevenly (see Figure 2A for a schematic illustration).
  • Uneven (irregular) distribution of cores 115 e.g., a spatial distribution that does not coincide with the spatial distribution of pixels on detector 91
  • the distribution of cores 115 and the interspaces across fiber 100 may be designed to optimize resolution enhancement using algorithmic and optical techniques. Indeed, increasing the distances between cores 115 may provide larger benefits from micro-scanning and application of other super resolution techniques.
  • the optical design of fiber tip 101 may be configured to have working channel 112 positioned asymmetrically and not centrally within the cross section of the tip (not concentric to the imaging channel).
  • the shape of working channel 112 may be configured to different than circular (e.g., elliptic, elongated, polygonal etc.) in order to better encode the optical transfer function (OTF).
  • OTF optical transfer function
  • the working channel shape may be configured to improve inversing the OTF and the algorithmic correcting of the image via the image post processing to yield a super resolved image.
  • an increased depth of focus may be achieved in lens-less embodiments by selecting the best focal positions that can provide the sharpest contrast per each pixel in the generated image, from images captured at different tip positions with respect to tissue 70.
  • the best focus for each pixel may be selected from a plurality of images captured at different tip positions.
  • optical elements 140 may be attached to or produced at distal fiber tip 100 (facing tissue 70). Optical elements 140 may be used to enhance imaging in both far-field imaging and near-field imaging. For example, optical elements 140 may be used to control the field of view, increasing it beyond the edges of tip 101 outwards and/or inwards (in case of a designed working channel void 112).
  • FIGS 4A-4D are high level schematic illustrations of hollow endoscope fiber 100 having optical elements 140 at distal tip 101 which compensate for the central void, according to some embodiments of the invention.
  • void(s) 112 at the cross section of fiber 100 at tip 101
  • various solutions are presented below for imaging a void-facing area 72 in addition to (or in place of) region 71 facing cores 115.
  • any type of target 70 may be imaged, e.g., tissue, specific anatomical members, bodily fluids, various stones or obstructions, tumors, foreign bodies etc.
  • illumination source 160 of endoscope 105 and at least some of the optical elements may be configured to image at least a part of the area facing void(s) 112 (e.g., void- facing area 72) differently than a rest of the region facing tip 101 (e.g., core-facing region 71).
  • the difference in the imaging may lie in any of polarization, wavelength, wavelength range and/or timing of the illumination. Non-limiting examples are presented in the following.
  • Multiple cores 115 may be used to generate a full image, overcoming the lack of cores in hollow region 112 and providing imaging (and illumination) of tissue 70 directly opposite to working channel 112 (void- facing area 72).
  • endoscope 105 may be configured to provide a 90° field of view of fiber 100.
  • Figure 4A schematically illustrates in a non-limiting manner an annular multicore region 110 (with an inner radius Ri and an outer radius R 0 ) having annularly arranged optical elements 140. Similar principles may be applied to any geometric configuration of fiber tip 100, e.g., any form thereof, any position and form of void(s) 112, etc.
  • optical elements 140 may comprise gradient index (GRIN) lenses cut at specified angles and glued at tip 101 of micro endoscope 105.
  • Each cut GRIN 140 may be cut and positioned to face a different direction in order to enhance the fiber's field of view (FOV) to equal the number of GRINs 140 multiplied by the FOV of each GRIN 140 (or, complementarily or alternatively, enhance the depth of field by configuring some of GRINs 140 to deliver radiation from different depths of field).
  • the cut of the edge of GRIN lenses 140 may realize a prism coupling light into that specific GRIN from different predefined sectors of the field of view.
  • Aspheric lenses may be used as alternative to GRIN lenses as optical elements 140.
  • FIGS 4B-4D schematically illustrates three possible configurations, according to some embodiments of the invention.
  • the large circle schematically represents the periphery of the total FOV of fiber tip 101, which is the boundary of the imaged region facing the cores (71), while the small circles represent the fields of view of individual optical elements 140, 141, taken in a non-limiting illustrative case to be equal.
  • tip FOV region 71 plus void-facing area 72
  • optical elements 140 may be covered by equally spaced (in Figure 4B eight) optical elements 140 each imaging a peripheral region 145, and an additional optical element 141 may be configured to image a central region 146.
  • Void- facing area 72 is thus covered centrally by region 146 and its periphery is covered by regions 145.
  • a larger number (in Figure 4C twenty one) of optical elements 140 may be configured to have angles covering tip FOV in several concentric circular sets of imaging regions - in the illustrated example twelve peripheral regions 145, eight intermediate regions 146 and one central region.
  • annularly arranged optical elements 140 in Figure 4D twenty five may be configured to have angles covering the tip FOV in a grid-like manner individual regions 145 partly overlapping and covering tip FOV and possible extending into a larger area. This disclosed method provides high flexibility in adapting fiber tip optical elements 140 to yield a required field of view.
  • optical element 140 may comprise an annular lens coupled to an annular prism that directs light from the whole FOV into the annular lens.
  • the center of FOV may be imaged using selective illumination. Illumination may be directed to the center of FOV and not to its periphery, and accompanying algorithms may be configured to process the detected signals to derive images of the FOV center (e.g., by processor 170).
  • illumination having different polarizations may be used for the central FOV (e.g., void-facing area 72) and for the periphery of FOV (e.g., cores- facing region 71), so that the detected signal is spatially encoded by the difference in polarization, and may be decoded to create images of the whole FOV (see more elaborate explanation below).
  • Optical elements 140 may be birefringent to directly differently polarized illumination to different geometric areas.
  • void 112 may be eccentric or divided into eccentric voids, leaving rooms for ventral cores to image the center of the FOV directly.
  • cores 115 may unequally or non-uniformly spaced within fiber 100, e.g., such that the positions of cores 115 do not coincide with the uniform spatial sampling matrix of the pixels of detector 91 positioned outside the body. The lack of coinciding between the two grids may be utilized to apply geometric super resolving algorithms to improve the quality of the captured image (resembling in a sense the micro- scanning technique).
  • fiber 100 may exhibit multicore designs having a low fill factor (the fill factor is the ratio between the core area and the square of the distance between cores, the latter termed pitch).
  • the core diameter may range between 0.4-2.5 ⁇ and the pitch may range between 2-10 ⁇ to yield a range of low fill factors (1 /(pitch/core diameter) 2 ), e.g., fill factors between 1 ⁇ 4 and 1/16.
  • the fill factor is low (e.g., below 1 ⁇ 4, below 1/9, e.g., 1/16)
  • simple movement of tip 101 of the micro endoscope e.g., movement amplitude may equal at least the pitch, e.g.
  • micro-scanning concept enable implementation of the micro-scanning concept to significantly increase the geometric resolution of the device.
  • the micro scanning procedure cannot increase the geometric resolution of the image but rather only to perform over-sampling of the image - because the point spread function (PSF) of the sampling pixel/core itself limits as a spatial low pass the obtainable resolution.
  • PSF point spread function
  • spatial scanning methods and temporal scanning methods according to the present disclosure may be combined and adapted to imaging requirements.
  • illumination channel 85 may have time-varying optics which realizes a spatial scanning of the illumination spot.
  • the spatial illumination scanning may be used to construct a wide field image having large field of view which is not affected by the working channel positioned in the center of the tip even if the tip is in near field with respect to the inspected tissue.
  • processor 170 may be configured to process into images radiation delivered from the imaging region through cores 115 to detector 91 and possibly to implement super-resolution algorithms on the detected radiation.
  • inspected tissue 70 may be illuminated by a tunable laser (e.g., as laser source 64) as illumination source 160.
  • a set of spatial images of tissue 70 may be captured, each image corresponding to a different wavelength.
  • the resulting is hyperspectral image may be used for identification of specific types of tissues (e.g., cancerous tissue) to enhance the imaging.
  • fiber endoscope 105 may provide diagnostic possibilities carried out using different wavelengths (in a specified diagnostic wavelength range, such as infrared wavelengths used to measure hemoglobin oxygenation) that are used for specific purposes and not necessarily for the imaging illumination.
  • multiple narrowband wavelengths 62 may be used to provide diagnostics with one or more wavelength combinations 174 by processor 170.
  • Such combinations may be achieved by using sources with fixed spectral ranges and/or tunable source(s) to change temporally the spectral composition of illumination 85.
  • Examples for diagnostics which may be achieved by wavelength combinations 174 include biopsy (diagnostics of removed tissue) and characterization of biological tissues in situ e.g., by measuring reflectance at different and very specific wavelengths.
  • a non-limiting example includes pulse oximetry which may be extracted by measuring a ratio of absorption at wavelengths of 600-750nm (e.g., at 660nm) and 850-1000nm (e.g., at 910nm), e.g., as two distinct wavelength (ranges) 62, utilizing the different spectral absorption curves of Hb0 2 and Hb.
  • wavelengths and wavelength bands may be changed during the procedure, manually or automatically, to adapt to different stages in the procedure and different imaging requirements with respect e.g., to spatial or temporal parameters, encountered site and tissue, etc.
  • single wavelength bands may be illuminated and analyzed separately, to enhance the derived information.
  • Given wavelength bands may be used to illuminate the target from different directions to yield more detailed spatial information.
  • working channel 112 of endoscope 105 configured as an ureteroscope may be used to suck out large kidney stones and attach the stones by suction to tip 101 of the endoscope.
  • Treatment laser possibly incorporated in fiber 100, see Figures 3A-3C
  • Suction may be applied through working channel 112, and the imaging may be used to provide feedback regarding the efficiency of the suction and the treatment. For example, intensive treatment may tend to overcome the suction and release the attached stone.
  • the imaging may be used to detect the development of stone disengagement from fiber tip 101 and to adjust suction and/or applied energy respectively.
  • splitting of energy application into several fibers as described above may provide more uniform treatment of the stone that employs lower energy concentration at any one point of the stone. Energy application intensity may be regulated at each of the energy sources to avoid stone disengagement from the suction.
  • working channel 112 of the ureteroscope may be used to inject liquid and to slightly change the optical conditions of fiber 100 such that effectively the focal length of lens 140 at tip 101 is changed and focal scanning can be realized to produce the sharpest possible image per each pixel in the image.
  • Endoscope 105 may be configured as any type of endoscope and be used to handle any type of bodily stones or other obstructions, for example, by laser treatment source 66.
  • Figures 5A-5C are high level schematic illustrations of optical elements 140, according to some embodiments of the invention.
  • a polarizing optical element 150 e.g., a Glan Thompson prism
  • Polarizing optical element 150 may be configured to increase FOV by polarization multiplexing beyond the limitations of optical element(s) 140.
  • Different fields of view 130A, 130B may be polarization- encoded, folded into endoscope fiber 100 and separated at the output (e.g., using a polarized beam splitter (PBS) 93 before reaching detectors 91, 92).
  • Polarization-encoding may be carried out using different linear polarization directions (e.g. with 45° therebetween), circular polarization etc.
  • Polarization multiplexing may be used to increase the imaged area either laterally or centrally (see above), depending on the configurations of fiber 100 and the optics.
  • Polarization multiplexing may be combined with temporal scanning of the field of view. Polarization multiplexing may be used to enhance three dimensional depth imaging in place or in addition to enlarging the field of view.
  • Illumination source 160 for polarization multiplexing may be non-polarized (with separation to polarization component being carried out optically), or polarized and have both components.
  • Figures 5B and 5C schematically illustrate embodiments for optical elements 140, 150 at fiber tip 101, namely an angle deflecting element 150 (e.g., a prism) and an imaging optical element 140 (Figure 5B) and a combined configuration with a faceted GRIN lens 140 ( Figure 5C).
  • an angle deflecting element 150 e.g., a prism
  • an imaging optical element 140 Figure 5B
  • Figure 5C Figure 5C
  • certain parts of FOV may be imaged by different optical elements 140 (and respective cores 115) to enable optical triangulation, e.g., distance measurement from tip 101 and the tissue region.
  • Such embodiments allow to trade-off FOV with depth information and thus dynamically allocate imaging resources (e.g., FOV - Field of View, DOF - Depth of Field) according to situation dependent needs.
  • different polarizations may be used by different optical elements 140 imaging the same region, so that using polarization enhances depth information instead or in addition to extending the FOV (as explained above). Dynamic variation of polarization may be used to modify the optical performance of fiber 100 during operation.
  • different wavelengths may be used by different optical elements 140 imaging the same region, so that using wavelength multiplexing (e.g., using a tunable laser as explained above) enhances depth information instead or in addition to extending the FOV (as explained above).
  • wavelength multiplexing e.g., using a tunable laser as explained above
  • Dynamic variation of color allocation may be used to modify the optical performance of fiber 100 during operation.
  • multiple laser sources having different wavelengths e.g., with multiple narrowband wavelengths 62
  • illumination source 160 e.g., four channels, three of which used to yield color imaging and the forth used to derive image depth information via triangulation computation.
  • the wavelength used for the fourth channel may be identical to the wavelength used in one of the other three channels to facilitate or simplify the triangulation computation.
  • endoscope 105 may be configured to use at least one non-imaged wavelength range, selected to provide additional depth of field or field of view information.
  • polarization, wavelength or spatial multiplexing may be used to image a tissue region from different directions, to enable stereoscopic vision of the tissue region.
  • Processor 170 may be configured to derive and provide stereo-imaging.
  • illumination 85 may be improved in quality in different respects, such as its white light spectrum 177 and beam profile 184, as disclosed above.
  • endoscope 105 may be configured to provide two or more levels of resolution, allow balancing field of view information and depth of field information, or allow balance between any other image parameters by adapting the illumination and/or the image processing procedure disclosed herein.
  • Figures 6A and 6B are high level schematic illustration of fiber cross sections with different configurations of the cores, according to some embodiments of the invention.
  • Figure 6C illustrates comparative experimental results of full core and hollow core fibers, according to some embodiments of the invention.
  • the configuration of the cores may be designed to reduce crosstalk between cores 115 and to be less affected by its banding.
  • crosstalk reduction may be achieved in the fabrication process by generating physical barriers between the cores or by using anti-crosstalk layer(s).
  • Core spacing may be selected to reduce crosstalk between adjacent cores 115 below a specified threshold.
  • crosstalk may be reduced by spacing the cores (e.g., by at least 4 ⁇ between cores) and by increasing the refraction index difference between the cores and the cladding.
  • the cores may be interspaced by structures such as air holes or doped polymer material (e.g., with incorporated nanoparticles).
  • Cores 115 may be hollow, made of polymer material and/or include nanoparticles to control the refractive index. In certain embodiments, contrast may be enhanced by placing the hardware with the external holes array.
  • an optical element e.g., optical element 94
  • the optical element may comprise an intensity mask having a value of one for all core locations and a value of zero for all cladding locations to make all and only information from the cores to propagate to detector 91.
  • the difference in the refraction index between cores 115 and cladding 113 may be designed to be large enough, and/or intermediate elements 111 may be introduced to reduce interaction between radiation propagating in different cores 115.
  • Core 115 and/or cladding 113 and/or elements 111 may comprise polymer with incorporated nanoparticles. Due to plasmonic resonance of the nanoparticles at specific wavelengths an effective increased refraction index may be obtained for the doped material.
  • the specific wavelengths may be selected to be close to wavelength bands (e.g., within a few nm, e.g., ⁇ 5nm at most) of illumination source 160 (e.g., three or four color lasers 62 and/or 64). It is noted that as both the plasmonic resonance and the bandwidth of illumination lasers are narrow, they may be matched to yield an effectively increased refractive index by the nanoparticles at the illumination wavelengths.
  • hollow cores through which no light coupling is obtained may be interlaced as intermediate elements 111 between cores 115 (see Figure 6A). Hollow cores 111 may be used to reduce the effective refraction index difference between light conducting solid cores 115 and their surrounding medium 113.
  • cores 115 may be hollow (Figure 6B) and be isolated by doped or non-doped solid polymer. Hollow cores 115 (air holes) were shown to very significantly reduce material losses (Figure 6C) and are thus exceptionally advantageous when using polymer fibers 100 which are characterized by relatively large losses compared to glass fibers.
  • the main advantage of polymer fibers is their flexibility, enable strong bending which is required under certain endoscope applications (e.g., treating kidney stones as presented above).
  • Fiber materials (for cladding 113 and intermediate elements 111 if any) and doping may be selected according to the required refractive indices and mechanical properties of fiber 100, and may comprise various types of biocompatible (or not biocompatible, e.g., in non-medical uses) polymers, possibly doped with nanoparticles to influence the refractive indices. Either or both illumination wavelength ranges and types of nanoparticles may be selected to optimize the changes in the refractive indices to optimize the radiation transfer through the cores.
  • core diameter Di, diameter of intermediate elements D 2 and distance between cores L may be configured to achieve specified optical performance parameters.
  • FIG. 7 is a high level schematic flowchart illustrating a method 200, according to some embodiments of the invention.
  • Data processing stages and control stages may be implemented by respective processors and algorithms may be implemented by respective computer program product(s) comprising a computer usable medium having computer usable program code tangibly embodied thereon, the computer usable program code configured to carry out at least part of the respective stages.
  • Method 200 comprises configuring an endoscope from a fiber with at least several hundred cores (stage 210), e.g., having a multi-core imaging region or a multi- core tip configured to deliver reflected illumination along the fiber for an external detector.
  • Method 200 may comprise implementing near-field imaging (target imaging at the fiber tip) (stage 212) and/or implementing far- field imaging (Fourier plane at the fiber tip) (stage 214).
  • method 200 may comprise configuring an endoscope from a plurality of fibers, grouped together, each having at least one hundred cores distributed at a fill factor smaller than 1 ⁇ 4, or even below 1/9, and at least one photonic illumination fiber, implementing three dimensional sensing by handling the cores group- wise with respect to radiation delivered therethrough, implementing super-resolved imaging by micro scanning over a pitch distance between the cores, and configuring at least one optical element at a distal tip of the fibers to enhance a field of view and/or a depth of field of the endoscope beyond a region facing a tip of the fibers and congruent thereto.
  • Method 200 may comprise at least one of the following stages for reducing losses and/or cross talk between cores: incorporating in the cladding, nanoparticles with plasmonic resonances that are in proximity to illumination (and imaging) wavelengths (stage 220); interspacing cores by intermediate elements (possibly incorporating nanoparticles) having a different refractive index than the cores (stage 230), e.g., by 0.1 ; interspacing cores by air holes (stage 235) and configuring cores as air holes (stage 240), and may comprise reducing crosstalk between adjacent cores by interspacing them (stage 245).
  • method 200 may further comprise incorporating one or more void(s) in the fiber as working channel(s) for treatment, suction and/or illumination (stage 250).
  • method 200 may further comprise splitting treatment and/or illumination into several fibers operating collectively (stage 260) and/or incorporating additional fibers at the periphery of the fiber or of the void(s) (stage 265).
  • Method 200 may comprise cooling incorporated fibers through the working channel (stage 267).
  • method 200 may further comprise controlling treatment and/or suction optically or automatically using optical input during the treatment (stage 270), and treating bodily stones by the endoscope, e.g., kidney stones with an ureteroscope configuration (stage 275).
  • Method 200 may further comprise using lens-less configurations, without any distal optical elements (stage 277) and/or using distal optical elements to control the field of view, the depth of field, implement image multiplexing and/or determine imaging parameters (stage 282), for example by attaching or producing optical element(s) at the fiber tip (stage 280).
  • Method 200 may comprise enhancing the field of view and/or the depth of field of the endoscope beyond a region facing the tip of the fibers and congruent thereto (stage 285).
  • Method 200 may comprise configuring the optical element(s) to image void-facing areas (stage 290), for example, using a lens with blocked aperture (stage 292); using multiple prisms which optically communicate with the cores (stage 295) and configuring the prisms to image void-facing areas (stage 300), e.g., associating each prism with one or more cores (stage 305); imaging void-facing areas using different polarization, wavelength, wavelength range and/or timing of the illumination (stage 310), in the former using birefringent optical elements for polarization multiplexing (stage 315).
  • method 200 may further comprise implementing super- resolution algorithms (on the detected radiation) to enhance resolution, field of view and/or depth of field (stage 320).
  • method 200 may further comprise reducing speckle patterns by using Barker codes for optimizing coherence modulation (stage 317).
  • Method 200 may further comprise deriving 3D data using structured light illumination and processing (stage 319) and possibly enhancing super resolution processing using the patterned illumination (stage 322) as done, e.g., in time multiplexing super resolving concepts.
  • Method 200 may further comprise beam-shaping the illumination at the distal tip (stage 324).
  • method 200 may further comprise any of: distributing the cores irregularly (with respect to detector pixel order) over the tip cross section (stage 332), distributing the cores at a small fill factor (stage 334), and implementing micro- scanning of the region facing the tip (stage 336).
  • method 200 may comprise enhancing images by optimizing pixel focus over different tip positions (stage 338), for example by selecting the best focus for each pixel from a plurality of images captured at different tip positions, and composing an enhanced imaged from the pixels at their selected best focus.
  • method 200 may comprise handling the cores groupwise, possibly with dynamic allocation of cores to groups, to implement wavefront sensing by each group (stage 340).
  • Method 200 may comprise implementing light field sensing, e.g., comparing light directions at different cores operating in near field and multi-mode.
  • method 200 may further comprise using non-imaged wavelengths to provide additional field of view and/or depth of field information (stage 350).
  • Method 200 may comprise collecting diagnostic data using, possibly non-imaged, diagnostic wavelength ranges (stage 360).
  • method 200 may comprise configuring the endoscope as a laparoscope or an ureteroscope (stage 370).
  • method 200 may further comprise configuring the illumination to have multiple narrowband wavelengths (stage 362) and possibly deriving diagnostic data from measurements at different wavelengths (stage 364) and/or enhancing super resolution processing using wavelength multiplexing with respect to the multiple narrowband sources (stage 366).
  • method 200 may further comprise providing wideband white illumination using a PCF with zero dispersion point(s) selected to yield spectral broadening (stage 368).
  • Method 200 may further comprise producing the fiber from standardized fiber modules (stage 380).
  • method 200 comprises packaging the fiber modules into desired fiber cross section forms or configurations (stage 382).
  • Method 200 may comprise modifying the spatial relations of the fiber modules along the fiber (stage 385), e.g., to have a circumferencial arrangement of fiber modules at the distal tip and a compact arrangement of fiber modules at the proximal tip of the fiber.
  • method 200 may further comprise applying conductive coatings to some fiber modules, with other fiber modules as insulators (stage 387), e.g., for delivering electromagnetic energy to the fiber tip via the conductive coating, e.g., for heating the fiber tip (stage 390), elements associated with the fiber tip and/or a surroundings of the fiber tip.
  • Method 200 may further comprise preventing fog upon and defogging the at least one optical element when required via a heated conductive coating thereof.
  • FIGS 8A-8E are high level schematic illustrations of experimental imaging results for bundled fibers, according to some embodiments of the invention.
  • the imaging configuration is illustrated schematically in Figure IB.
  • the presented results represent raw data, prior to the application of the image processing algorithms described above.
  • Figures 8A-8C illustrate the imaging of three different targets using a two by two bundled fiber (as evident in the four sub-images, each received from one fiber module, having a side of 450 ⁇ and ca. 23,000 cores per fiber module).
  • the targets are respectively a resolution target, characters (person and doll) and an anatomy model.
  • Figure 8D illustrates imaging by a single multicore fiber, 1.8mm in diameter having ca. 500,000 cores. Both configurations achieve very high resolution which is unattainable by current fibers.
  • Figure 8E illustrates a result achieved by applying image enhancement algorithms applied on the captured image.
  • Figures 9A-9D are images that provide examples for performance of endoscope 105, according to some embodiments of the invention.
  • Figure 9A illustrates an example for the multicore configuration of fiber 100, in the illustrated non-limiting case, fiber 100 has an external diameter of 0.45mm and includes more than 80,000 cores as well as an integrated illumination channel.
  • the bottom image is a magnified view of the marked section in the top image.
  • Figure 9B illustrates image examples by endoscope 105 of a fingernail (a), a mouth (b), teeth (c) and a fingertip (d). These images were taken using fiber 100 with external diameter of 0.45mm that includes more than 80,000 cores, and were processed as disclosed above.
  • Figures 9C and 9D illustrate examples for processing steps, namely the removal of artifacts and core traces (shown in Figure 9C) and the improvement of resolution and magnification (examples for the quality improvement of the results is shown in Figure 9D).
  • disclosed image processing algorithms provide the cleaned image of Figure 9D at a resolution of 300,000 pixels.
  • the images obtained from multicore fibers 100 are steady and are not influences by fiber bending, outperforming prior art multimode fibers.
  • very thin endoscope 105 provides high resolution medical imaging combined with high maneuverability and compliance with many medical situations.
  • Certain embodiments of the invention may include features from different embodiments disclosed above, and certain embodiments may incorporate elements from other embodiments disclosed above.
  • the disclosure of elements of the invention in the context of a specific embodiment is not to be taken as limiting their used in the specific embodiment alone.

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Abstract

La présente invention concerne des endoscopes, des fibres multicœurs d'endoscopes ainsi que des méthodes de configuration et de mise en œuvre associées. Les fibres peuvent comprendre des centaines ou des milliers de cœurs et éventuellement incorporer un ou plusieurs canaux opérateurs et des fibres supplémentaires. La fibre peut être utilisée dans des configurations optiques différentes pour capturer des images de tissu et d'objets au niveau de la pointe distale et pour améliorer une large gamme de caractéristiques optiques des images telles que la résolution, le champ de vision, la profondeur de champ, les plages de longueurs d'onde, etc. Une imagerie en champ proche ainsi qu'une imagerie en champ lointain peuvent être mises en œuvre dans les endoscopes et les caractéristiques optiques respectives peuvent être utilisées pour optimiser l'imagerie. Des éléments optiques peuvent être utilisés au niveau de la pointe distale de la fibre, ou la pointe distale de la fibre peut être exempte de lentille. Des boucles de rétroaction de diagnostic et de traitement optique peuvent être mises en œuvre et l'éclairement peut être conçu pour produire des images de couleurs pures, une estimation de profondeur, une amélioration de champs de vision et/ou des profondeurs de champ, et des données diagnostiques supplémentaires.
EP17883995.7A 2016-12-22 2017-12-21 Sources d'éclairement d'endoscopes à fibres multicoers Withdrawn EP3559723A4 (fr)

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US15/387,805 US10398294B2 (en) 2014-07-24 2016-12-22 Illumination sources for multicore fiber endoscopes
PCT/IL2017/051372 WO2018116302A1 (fr) 2016-12-22 2017-12-21 Sources d'éclairement d'endoscopes à fibres multicœurs

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JP7080195B2 (ja) * 2019-02-19 2022-06-03 富士フイルム株式会社 内視鏡システム
CN111297309B (zh) * 2020-03-07 2024-01-30 陕西艾诺美瑞申医疗科技有限公司 一种医学影像成像用电子内窥镜
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US6747795B2 (en) * 2000-06-30 2004-06-08 The General Hospital Corporation Fiber-coupled multiplexed confocal microscope
US6747781B2 (en) * 2001-06-25 2004-06-08 Silicon Light Machines, Inc. Method, apparatus, and diffuser for reducing laser speckle
WO2005119328A1 (fr) * 2004-06-03 2005-12-15 University Of Strathclyde Source lumineuse amelioree pour microscope a balayage
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US8471193B2 (en) * 2009-03-05 2013-06-25 Olympus Corporation Photodetection device for detecting low temporal coherence light, photodetection method, microscope and endoscope
WO2012093401A1 (fr) 2011-01-05 2012-07-12 Bar Ilan University Système et procédé d'imagerie utilisant une fibre à plusieurs cœurs
JP6010895B2 (ja) * 2011-11-14 2016-10-19 ソニー株式会社 撮像装置
JP6794352B2 (ja) * 2014-07-24 2020-12-02 ゼット スクエア リミテッド 多芯ファイバー内視鏡
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