US20160357007A1 - Fixed distal optics endoscope employing multicore fiber - Google Patents

Fixed distal optics endoscope employing multicore fiber Download PDF

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US20160357007A1
US20160357007A1 US15/147,775 US201615147775A US2016357007A1 US 20160357007 A1 US20160357007 A1 US 20160357007A1 US 201615147775 A US201615147775 A US 201615147775A US 2016357007 A1 US2016357007 A1 US 2016357007A1
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optical
fiber
endoscope system
receiver
endoscope
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US15/147,775
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Eric Swanson
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Priority to US15/147,775 priority Critical patent/US20160357007A1/en
Publication of US20160357007A1 publication Critical patent/US20160357007A1/en
Priority to US16/704,851 priority patent/US11256080B2/en
Priority to US17/676,129 priority patent/US11852802B2/en
Abandoned legal-status Critical Current

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Definitions

  • This disclosure relates generally to endoscopic devices and in particular to a fixed distal optics endoscope having multicore fiber.
  • NDE/NDT nondestructive evaluation/nondestructive testing
  • An advance in the art is made according to an aspect of the present disclosure directed to endoscopic devices employing multicore optical fiber.
  • devices constructed according to the present disclosure may employ—in addition to multicore optical fiber—employ a variety of measurement techniques including swept-source techniques, employ widely tunable source(s), include multiple functions, and—in some embodiments—critical complex optical functions may be performed by one or more photonic integrated circuit(s).
  • An illustrative endoscopic system and structure includes an optical receiver selected from the group consisting of spectral domain optical coherence tomography (OCT) receiver, time domain OCT receiver, confocal receiver, fluorescence receiver, and Raman receiver; an endoscope body including fixed distal optics; and a multicore optical fiber optically coupling the fixed distal optics to the receiver.
  • OCT spectral domain optical coherence tomography
  • endoscope is used throughout the disclosure to describe structures according to the present disclosure.
  • Those skilled in the art will readily appreciate that the disclosure is not specifically limited to endoscopes. More particularly, the disclosure and underlying principles herein are equally applicable to catheters, laparoscopes, imaging guidewires as well as other medical and non-medical devices and structures. Accordingly, when the term endoscope is used, it is intended that it be interchangeable with any instrument or system used to examine the inside of something—oftentimes a body for medical reasons. Such instruments advantageously permit the interior of an organ or other cavity of the body. Of further advantage, endoscopes are capable of being inserted directly into an organ for subsequent examination.
  • FIG. 1 shows exemplary Prior Art endoscopes
  • FIG. 2(A) , FIG. 2(B) and FIG. 2(C) show a series of exemplary single-mode fiber scanning endoscopes as known in the Prior Art;
  • FIG. 3 shows a schematic diagram of a multi-core fiber endoscope employing an array of swept-source optical coherence tomography (SS-OCT) receivers according to an aspect of the present disclosure
  • FIG. 4 shows a schematic diagram of a multi-core fiber endoscope employing a single SS-OCT receiver and distinct delays according to an aspect of the present disclosure
  • FIG. 5 shows a schematic diagram of another multi-core fiber endoscope employing a single SS-OCT receiver and 1:N switch(es) interconnecting the receiver to the endoscope according to an aspect of the present disclosure
  • FIG. 6 shows a schematic diagram of an illustrative distal portion of a five-core optical fiber endoscope according to an aspect of the present disclosure
  • FIG. 7(A) , FIG. 7(B) , FIG. 7(C) , FIG. 7(D) and FIG. 7(E) show a series of illustrative arrangements as schematic diagrams other illustrative multi-core fiber endoscope employing: FIG. 7(A) a collimating lens, FIG. 7(B) a fiber/lens coupling element including a passive or active beam steering elements, FIG. 7(C) a graduated index (GRIN) lens or section of multimode fiber, FIG. 7(D) a multi-element collimating lens, and FIG. 7(E) a beam deflector element according to aspects of the present disclosure;
  • FIG. 8 shows a schematic diagram of an illustrative multi-core fiber endoscope wherein the multi-core fiber is connected to a photonic integrated circuit (PIC) according to an aspect of the present disclosure
  • PIC photonic integrated circuit
  • FIG. 9 show another schematic diagram illustrating a multi-core fiber endoscope wherein the multi-core fiber is connected to a PIC according to an aspect of the present disclosure
  • FIG. 10 shows yet another schematic diagram illustrating a multi-core fiber endoscope wherein the multi-core fiber is connected to a PIC according to an aspect of the present disclosure
  • FIG. 11 show a schematic diagram illustrating a multi-core fiber endoscope having a pull-back and/or rotational or twisting proximal motor according to an aspect of the present disclosure
  • any element expressed as a means for performing a specified function is intended to encompass any way of performing that function including, for example, a) a combination of circuit elements which performs that function or b) software in any form, including, therefore, firmware, microcode or the like, combined with appropriate circuitry for executing that software to perform the function.
  • the invention as defined by such claims resides in the fact that the functionalities provided by the various recited means are combined and brought together in the manner which the claims call for. Applicant thus regards any means which can provide those functionalities as equivalent as those shown herein.
  • imaging endoscopes such as those employed in optical coherence tomography systems—typically employ single mode optical fiber.
  • Such systems perform scanning and imaging by either: 1) spinning the fiber or 2) employing distal optics—for example, motor(s) and actuator(s)—along with a stationary single mode optical fiber.
  • distal optics for example, motor(s) and actuator(s)—along with a stationary single mode optical fiber.
  • configurations such as 1) and 2), above, provide necessary beam deflection(s) to effect the scanning.
  • FIG. 1 there is shown several illustrations of contemporary optical endoscopes that are known in the art. While not specifically identified in that Figure, such endoscopes may include an eyepiece, a light post, and an objective assembly. Alternative configurations may include—among other things—an access port for instrument(s) and an “umbilical” connection.
  • FIG. 2(A) , FIG. 2(B) and FIG. 2(C) show in schematic form several illustrative examples of single-mode, or multi-mode fiber scanning endoscopes as known in the art.
  • such endoscopes must be capable of delivering, focusing, scanning and collecting a single spatial-mode optical beam.
  • the catheter employed oftentimes is flexible—but not always—and has a sufficiently small diameter to facilitate its entry into internal spaces such as arteries.
  • such endoscopes will include optical control and coupling element(s) at a proximal end, a single-mode fiber running the length of the catheter, and optical focusing and beam directing elements at the distal end.
  • the endoscope is configured to scan the beam in a circumferential pattern such that a cross-section image may be made of structure(s) into which it is positioned such as—for example—an artery.
  • such illustrative examples generally include—at a proximal end—a system 210 which may include light source(s), detector(s) and controlling circuitry and/or operating software(s).
  • a system is optically, mechanically, and electrically coupled to a catheter body 230 by a rotary fiber optical joint 220 which includes a spinning optical fiber 231 which in turn is connected—at a distal end—to one or more lens(es) 240 and prism 241 which in turn produces a spatial mode optical beam 250 .
  • FIG. 2(B) includes—at its proximal end—system 212 , stationary fiber optical joint 213 which is coupled to catheter body 232 and includes a fixed, or stationary, otherwise non spinning single mode optical fiber 233 which in turn is coupled—at the distal end—to one or more lens(es) 242 which in turn is optically coupled to a prism 243 which is spun by distal motor 253 .
  • FIG. 2(C) includes system 214 , stationary fiber optical joint 224 , catheter body 234 including stationary single mode optical fiber 235 optically coupled at a distal end to lens(es) 244 and optical phased array(s) 245 thereby producing scanning beam 256 .
  • spinning optical fibers such as those employed in configurations such as that in FIG. 2(A)
  • Distal motors such as those employed in FIG. 2(B)
  • Distal optical phased arrays such as those employed in FIG. 2(C) —while offering optimistic promise nevertheless exhibit limitations with respect to image quality, efficiency sidelobes, electrical power requirements and size.
  • scanning optical endoscopes exhibiting low cost, small size and acceptable (albeit lower) scanning resolution may be may be constructed according to aspects of the present disclosure. More particularly, and with reference to FIG. 3 , there is shown in schematic an illustrative multi-core fiber endoscope 300 according to an aspect of the present disclosure employing an array of swept-source optical coherence tomography (OCT) receivers. As shown in that figure, a multi-core optical fiber is employed and—in sharp contrast to the prior art—no distal mechanical element(s), controllable phased array(s), and/or spinning fibers are used. Of further advantage, individual optical fibers employed may be single-mode fiber(s) or multi-mode fiber(s).
  • OCT optical coherence tomography
  • a multi-core fiber has multiple cores positioned within a cladding.
  • MCF multi-core fiber
  • Such MCF have been employed in telecommunications applications and shown considerable promise.
  • the number of cores comprising a MCF may differ from application to application—as those individual application needs dictate.
  • a seven core MCF may have one center and six outer cores.
  • the distance between two neighboring cores is known as the core pitch.
  • the core pitch By altering the core pitch—it is known by those skilled in the art—that the amount of crosstalk between neighboring cores may be changed.
  • a swept-source optical coherence tomography system 310 is coupled to a multi-core optical fiber endoscope 330 .
  • either single-mode or multi-mode fibers may be employed however for SS-OCT systems such as the one illustrated single-mode fibers are preferably used.
  • SS-OCT systems such as the one illustrated single-mode fibers are preferably used.
  • any of a variety of measurement system(s) may be employed and remain consistent with one or more aspect(s) of the present disclosure.
  • a swept source laser 312 is split into N different channels through the effect of splitter 313 or other suitable optical structure(s), each of the N channels optically coupled to a multi-core optical fiber 324 via a proximal end connected (shown in Figure as a dotted line).
  • the N channels are conveyed via the multi-core optical fiber to distal optical structure(s) 370 that may focus light through a transparent, protective cover 360 —or transparent windows in a transparent cover—such that output light 380 is conveyed into any external sample, i.e., body tissue(s) or cavities.
  • an endoscope such as the one illustrated 330 may include a protective and/or structural jacket 340 to ensure integrity and/or smooth operation/insertion of the device as it is routed through other instruments or directly into a body lumen or other sample environment.
  • the distal optical structures may advantageously include one or more passive lens assemblies or photonic integrated circuit(s) (PIC).
  • PIC photonic integrated circuit
  • planar lightwave circuits (PLC) comprising those optical structures may advantageously be fabricated from InP or Si photonic materials—among others.
  • contemporary design tools may be employed to design, simulate and manufacture the distal optical structures while producing benefits related to high precision, small size and low-cost.
  • distal optics according to the present disclosure may be fabricated—either in whole or in part—from molded optical materials and components thereby further lowering their cost and manufacturability.
  • the distal optics of the system so described may comprise one or more PICs—so may elements of the SS-OCT portion 310 of the system. More particularly, on one illustrative embodiment according to the present disclosure—the SS-OCT portion of the system 310 shown schematically within the dotted line of FIG. 3 , (excluding any elements/components not suitable for PIC fabrication presently—i.e., computers, etc.) may comprise one or more PICs such that a compact, robust, low-cost structure(s) result. As those skilled in the art will further appreciate and as will become apparent to those skilled in the art, such PIC fabrication methodologies may advantageously be applied to other designs/configurations according to the present disclosure including those described herein.
  • a vertical cavity surface emitting laser (VCSEL) or other laser structure such as verner tuned laser may be integrated into an SS-OCT PIC such that a single PIC includes a VCSEL transmitter, waveguide(s) for beam handling and one or more optical receivers such as a dual-balanced, dual-polarization, I/Q receiver—among other(s).
  • VCSEL vertical cavity surface emitting laser
  • I/Q receiver optical receiver
  • FIG. 4 there is shown a schematic of an illustrative embodiment of a multi-core fiber endoscope system 400 employing a single SS-OCT receiver and distinct delay(s) according to an aspect of the present disclosure.
  • a single receiver 410 is employed and SS-OCT information from each optical fiber comprising the multi-core fiber 425 is extracted through the utilization of distinct delays 414 (D . . . Dn).
  • distinct delays 414 D . . . Dn
  • information about optical properties from each path is transformed into distinct intermediate frequencies (i.f.) at any photodetector(s) used.
  • PS-OCT polarization sensitive OCT
  • DSP unit 417 may process these n distinct if. frequencies as they arrive as different—and substantially non-overlapping—frequency bands.
  • DSP unit 417 may process these n distinct if. frequencies as they arrive as different—and substantially non-overlapping—frequency bands.
  • the receiver 410 is coupled to the endoscope 430 by the multicore optical fiber 425 , wherein each of the individual fibers comprising the multicore optical fiber includes one or more distinct delay elements 414 (D. . . . Dn) which produces a distinct delay for each of the individual fibers.
  • the endoscope 430 generally includes a body—providing a protective and structural jacket 440 to the multicore fiber 425 as well as other elements positioned therein and comprising the overall endoscope 430 .
  • distal optics 470 produce optical scan beams 480 and is generally protected through the effect of cap, 460 .
  • a variety of distal optical configurations are contemplated according to the present disclosure.
  • FIG. 5 shows yet another illustrative embodiment of a multi-core optical endoscope system 500 according to the present disclosure wherein an illustrative SS-OCT sub-system 510 is coupled to a multi-core optical fiber endoscope sub-system 530 through the effect of a 1:N switch 524 .
  • the illustrative sub-system 510 inlcudes a number of circulators 514 along with receiver 516 and DSP 518 for receiving and processing return signals from samples illuminated by beams 580 and under examination by endoscope system 500 .
  • repetition rate of laser 512 may be synchronized to the switching rate of the 1:N switch 524 such that light is transmitted and received substantially during a single frequency sweep (or multiple thereof).
  • repetition rate of laser 512 may be synchronized to the switching rate of the 1:N switch 524 such that light is transmitted and received substantially during a single frequency sweep (or multiple thereof).
  • inefficiencies associated with switching dynamics are incurred during a period when the laser is blanked—at lower power.
  • unused portion(s) of the laser frequency sweep is overlapped in time with unusable portions of the switching during switching transients.
  • FIG. 6 there is shown in schematic form another illustrative embodiment (both side and end view(s)) of a distal end of multi-core fiber endoscope 600 according to an aspect of the present disclosure.
  • the distal end of the endoscope includes a protective cap 670 and distal optics including collimating lens(es) 673 , fold mirrors 672 , and substrate 671 coupled to the multi-core fiber, 625 which in this illustrative embodiment includes 5 (five) single optical fibers shown arranged as a central fiber with four perimeter fibers.
  • the number of individual fibers and number(s) of individual distal optical elements may be changed as specific application needs dictate. Additionally, the arrangement of the individual fiber(s) and distal optical element(s) may change from application to application as well. Shown further in that Figure is the light beam patters 675 which emanate from the distal optics.
  • lens(es) may be graduated index (GRIN) lenses, ball lenses, fiber lenses, and/or lens arrays including multimode, multicore fiber lens that may be affixed or fusion spliced to the distal end of the multi-core fiber.
  • Optional fold mirrors or prisms or other structures
  • one or more center cores may be coupled to optical structures (lenses, etc) that direct light substantially along the endoscope axis.
  • distal optical elements may be made from discrete components, one or more molded components, photonic integrated circuit(s) or combinations therof.
  • a protective cap may be fully or partially transparent or include windows to allow light to traverse from optical fibers and/or optical elements to/from samples under examination while providing a smooth, sufficiently strong, and appropriately shaped character such that it may be presented/inserted/retrieved from anticipated pathways such as the interior of a bodily lumen.
  • the entire distal optics may be assembled and/or fabricated as part of or on top of a substrate.
  • the substrate may allow beam expansion from fiber to lens(es) such that a desired focus, beam waist etc. may be realized.
  • the core size is ⁇ 9 um.
  • to a achieve a ⁇ 20 um beam waist (1/ê2) at a ⁇ 1 mm focal length requires ⁇ 28 um diameter (1/ê2) at a face of a lens (in air).
  • Longer focal lengths require a correspondingly larger beam diameter at the lens face where requires a larger lateral separation between fiber cores in the multicore fiber.
  • it is desirable that light propagating along the fiber cores and up to and out of any lense(s) does not have substantial leakage from one channel to another.
  • alternative illustrative embodiments of the arrangement of FIG. 6 may not necessarily include the lens(es) depicted in that Figure.
  • one or more fold mirrors may be employed to redirect light into/away from the fiber axes—as appropriate.
  • imaging range may be achieved ( ⁇ 0.3 um the Rayleigh range assuming a 1310 nm wavelength and a ⁇ 9 um beam waist at fiber facet). Accordingly—and as will be readily understood by those skilled in the art—there are a variety of other focal length/focal spot size width exit beam diameter design tradeoffs that may be made depending on the desired operating parameters.
  • Such applications include where a precise, continuous profile of an intimal surface of a lumen is not needed but a measurement of 2, 4, or 8 cross sectional dimensions of the lumen opening is sufficient.
  • a nine core optical fiber with one fiber as a central fiber and eight fibers positioned concentrically around the perimeter of that central fiber—each perimeter fiber having a fold mirror associated with it—then four cross-sectional measurements along the 0, 45, 90 and 135 degree axis may be made along with one forward axial measurement.
  • Such measurement(s) may be combined with fiber pull-back mechanism(s) to pull (or push) the endoscope substantially along the axis of the fiber. As will be shown and discussed, it is possible to perform a manual or automated twisting action—back and forth—to sample more of the circumferential area of interest. In this manner four cross-sectional measurements may continuously be made as the endoscope/fiber is pulled back. Such measurement(s) may be useful for a variety of applications including sizing lumens for stents or other therapeutic or interventional procedures.
  • endoscope(s) may be combined with other measurement devices/techniques including optical measurements (fluorescence, NIR, Raman) or non-optical devices (e.g., pressure, temperature, pH, etc.) It is also possible to combine such device(s) with therapeutic devices such as surgical lasers, cryo or RF ablation, mechanical cutting tools, and/or other devices/structures. Of distinct advantage, it is possible to position such devices within the inside of a needle—due to its small size.
  • FIG. 7(A) , FIG. 7(B) , FIG. 7(C) , FIG. 7(D) and FIG. 7(E) show a series of illustrative arrangements as schematic diagrams other illustrative multi-core fiber endoscope employing: FIG. 7(A) a collimating lens, FIG. 7(B) a fiber/lens coupling element including a passive or active beam steering elements, FIG. 7(C) a graduated index (GRIN) lens or section of multimode fiber, FIG. 7(D) a multi-element collimating lens, and FIG. 7(E) a beam deflector element—as part of distal optics all according to certain aspects of the present disclosure.
  • FIG. 7(A) a collimating lens FIG. 7(B) a fiber/lens coupling element including a passive or active beam steering elements
  • FIG. 7(C) a graduated index (GRIN) lens or section of multimode fiber
  • FIG. 7(D) a multi-e
  • FIG. 7(A) shows another illustrative example of a multi-core fiber endoscope 700 according to the present disclosure wherein a single, shared collimating lens 710 is employed to collimate multiple outputs 715 from multi-core optical fiber 730 .
  • the lens may be a single element lens that is coupled to the multi-core fiber 730 via a free-space or solid coupling mechanism(s) 720 including direct fusion splice of a graded index lens constructed of optical fiber or cementing a GRIN lens to the end of the multi-core fiber.
  • the lens so coupled may be a single element or multiple, separate elements.
  • Such lens(es) may be a GRIN lens, ball lens or aspheric molded glass lens—among other types as well.
  • lensing element(s) using fiber gratings within the core or cladding material of the multi-core fiber.
  • a fiber/lens coupling element 720 includes a passive or active beam steering element(s) 721 , i.e., a prism element, to adjust the focus location of light emanating from each of the individual fibers comprising the multi-core fiber (shown emanating onto a collimating lens 710 ) such that the focus location(s) are nearly identical with respect to any sample(s) being examined.
  • a passive or active beam steering element(s) 721 i.e., a prism element
  • N cores in the multi-core fiber there are a number of approaches to this illustrative example.
  • all N cores may be utilized in parallel using receiver structure(s) shown previously.
  • a single fiber for example the center fiber—emits light and the remaining fibers—or a subset of the remaining fibers—may simultaneously be used to collect light reflected from the sample(s).
  • beam waists are in the same—but not necessarily exact same) location and additional information about angular scattering and back reflection of light from the sample may be obtained and used to differentiate tissue structure.
  • using one (or more) of the individual fibers comprising the multi-core optical fiber to illuminate and using other fibers to collect light reflected from the sample(s) may be extended to any of the embodiments contemplated herein or derivatives therof.
  • FIG. 7(C) shows yet another illustrative embodiment of a multi-core optical fiber endoscope 702 according to an aspect of the present disclosure.
  • a lens employed may advantageously be a GRIN lens or a section of multimode fiber exhibiting a property to image facets of the multi-core fiber at an appropriate distal beam focus.
  • the use of a multimode fiber, as is known in the art, is particularly attractive since it may be fusion spliced or otherwise easily secured to the end of the multicore fiber.
  • the beam may enter a beam propagation region 735 .
  • an optional distal beam deflector 740 element can be used to deflect some of the beams 742 substantially away from the axis of the endoscope and allow one or more or no beam to pass through substantially uninterrupted to allow for forward ranging 743 .
  • the endoscope can have transparent windows at appropriate beam exit locations and as noted previously—when smooth—allows for easier insertion into tight spaces.
  • an outer sheath of the endoscope body may be made transparent and constructed from a biocompatible materials.
  • FIG. 7(D) shows yet another illustrative embodiment of a forward imaging multicore fiber endoscope 703 having a multi-element collimating lens and distal beam deflector element 740 .
  • a multi-element fiber/lens coupling element 720 is employed to individually collect light from each of the individual multicore fiber outputs 715 and direct/focus it such that the light may be more particularly directed onto/into a sample (not specifically shown).
  • such multi-element fiber/lens coupling element 720 may comprise a multi-mode, multicore optical fiber that is fusion spliced or otherwise connected to a single mode multi-core fiber.
  • the outside diameter of the multi-mode multicore fiber is substantially the same as the outside diameter of the single-mode multicore fiber.
  • other applications may advantageously utilize configurations in which the outer diameters are not the same—for example, those applications in which a larger exit beam diameter is desired.
  • the multi-mode multi-core fiber is configured with an appropriate GRIN-like profile to achieve appropriate beam parameters for example, focal distance, confocal parameter, etc. for imaging light onto/into the sample (not specifically shown).
  • the illustrative embodiment shown in the FIG. 7(E) includes a beam deflector element, that is configured to direct one or more light beams 742 in a direction substantially away from the endoscope axis 751 such that they may be directed to the sample.
  • FIG. 8 shows yet an additional illustrative example according to the present disclosure in which a multicore fiber 810 is coupled to a photonic integrated circuit (PIC—or Integrated Optical Substrate) 820 .
  • PIC photonic integrated circuit
  • FIG. 8 shows yet an additional illustrative example according to the present disclosure in which a multicore fiber 810 is coupled to a photonic integrated circuit (PIC—or Integrated Optical Substrate) 820 .
  • PIC photonic integrated circuit
  • FIG. 9 there is shown an additional illustrative example of multicore optical fiber endoscope distal end 900 according to yet another aspect of the present disclosure. More particularly and as depicted in that Figure, the multicore optical fiber 930 is shown coupled to a photonic integrated circuit 920 . As depicted therein, light from the multicore fiber (not specifically shown)—which is butt coupled to the integrated substrate of the PIC 920 wherein it propagates via waveguide structures 925 to one or more surface grating coupler(s) 935 .
  • inner grating couplers 935 couple light to/from the waveguides 930 and multicore optical fiber as well as additional waveguides 939 which convey light from inner couplers 935 to/from outer surface grating couplers 937 which emit/receive light to/from sample(s).
  • waveguides For simplicity, only a single waveguide is shown connecting optical fibers to respective inner surface grating couplers and subsequently to outer grating couplers.
  • two or more waveguides may be employed to couple the optical fibers to the inner grating as well as two or more waveguides to couple the inner grating couplers to the outer grating couplers such that one or two polarization modes are conveyed.
  • the number of waveguides connecting the couplers does not have to be the same for each.
  • configurations according to the present disclosure such as that shown in FIG. 9 provide an advantage namely that the radius of the multicore fiber employed may be smaller and still provide a large aperture on emitting surface grating coupler.
  • FIG. 10 shows yet another illustrative example according to the present disclosure of a multicore optical fiber endoscope configuration 1000 wherein the multicore optical fiber 1030 is coupled to a photonic integrated circuit (integrated optical substrate) 1020 .
  • the individual cores 1031 of the multicore fiber 1030 are directly butt coupled to a surface grating coupler(s) 1035 fabricated in/on the circuit substrate 1020 .
  • the surface grating coupler(s) so coupled to the fibers 1031 are further coupled to respective end facet emitter(s) 1037 via respective optical waveguide(s) 1039 .
  • the end facet emitter(s) 1037 emit light substantially orthogonally to the axis of the multicore fiber (except for a center core).
  • end facet (horizontal) couplers there exist a number of end facet (horizontal) couplers that may be used including adiabatic coupling approaches.
  • a number of the illustrative embodiments shown exhibit a central fiber comprising the multicore fiber which is shown in the Figures to emit light along the axis of the fiber (forward).
  • the individual fibers comprising the multicore fiber do not all have to be the same.
  • a combination of different fibers may be employed where—for example—some fibers are single mode while others are multimode fibers.
  • some of the fibers may be employed for imaging and sensing while others may be used for invasive or other therapeutic procedures or other diagnostic modalities.
  • the measurement range e.g. the confocal parameter or 2 ⁇ the Rayleigh Range
  • the resolution at the beam waist e.g. the confocal parameter or 2 ⁇ the Rayleigh Range
  • the tighter the beam waist the higher the lateral resolution but the shorter the measurement range.
  • One of the attractive features of PIC and other integrated optical designs is that by using the high-resolution lithographic techniques for manufacturing the PICs one can make very complex amplitude and/or phase masks in the surface gratings.
  • Bessel beam generation and other similar depth-of-filed extension techniques, may be designed into the phase mask to provide extended measurement range for a given lateral resolution.
  • Such depth-of-field extension techniques can be designed into the surface grating couplers using PIC design tools and are advantageously applicable embodiments according to the present disclosure shown and described.
  • one of the advantages of using a multicore fiber is that it allows several simultaneous beams to be guided up/down the endoscope for sensing, imaging, and ranging.
  • One application of such an endoscope acquires several readings of an interior dimensions of a lumen and/or measures properties of interest of the lumen wall.
  • a single core configuration having a distal motor or a rotating fiber can produce a continuous measurement of a lumen, such an approach comes with noted disadvantages including increased cost, size, and complexity of the endoscopic probe.
  • Multicore fiber configurations according to the present disclosure have the potential to be smaller and therefore be employed into tighter lumens and medical devices (e.g. imaging needles).
  • FIG. 11 there is shown a multicore fiber endoscope 1100 including a pull-back (or push-back) and/or torsional element 1150
  • a pull-back or push-back
  • torsional element 1150 Such an element allows for the manual and/or automated pulling-back (or pushing forward) of the distal end of the endoscope along the axis of the endoscope body and lumen in which it is positioned. In this manner, optical measurements may be made along the axis of the lumen which advantageously allows several two-dimensional images to be obtained.
  • the entire multi-core fiber may be rotated back and forth (to and fro) as to radially scan the distal end of the endoscope and therefore the lumen/sample. This advantageously allows additional regions of the sample to be measured. It is also contemplated to have both pullback capability and twisting back and forth capability.
  • illustrative embodiments according to the present disclosure have depicted a number of ways to image light from a multicore fiber into a sample. There are of course other methods and combinations of the methods shown that may be implemented and are contemplated herein. Additionally, there are also many other aspects of a fiber endoscope design known in the art while not specifically shown and described. Such aspects include protective jackets (metal or plastic), torque cables, markers for x-ray, CT, or MM imaging, etc.

Abstract

Disclosed herein are configurations for fiber optic endoscopes employing fixed distal optics and multicore optical fiber.

Description

    CROSS REFERENCE TO RELATED APPLICATIONS
  • This application claims the benefit of United States Provisional Application(s) 62/157,131 filed May 5, 2015; 62/163,522 filed May 19, 2015; 62/163,532 filed May 19, 2015; and 62/166,154 filed May 26, 2015 the entire contents of each are incorporated by reference in their entirety as if set forth at length herein.
  • TECHNICAL FIELD
  • This disclosure relates generally to endoscopic devices and in particular to a fixed distal optics endoscope having multicore fiber.
  • BACKGROUND
  • Medical and non-medical applications of imaging endoscopes are well known and their importance to contemporary cardiology, gastroenterology, pulmonology, laparoscopy as well as nondestructive evaluation/nondestructive testing (NDE/NDT) is widely accepted. Given that importance, improvements to endoscopic devices and systems would represent a welcome addition to the art.
  • SUMMARY
  • An advance in the art is made according to an aspect of the present disclosure directed to endoscopic devices employing multicore optical fiber.
  • In contrast to contemporary, prior-art endoscopic devices and systems, devices constructed according to the present disclosure may employ—in addition to multicore optical fiber—employ a variety of measurement techniques including swept-source techniques, employ widely tunable source(s), include multiple functions, and—in some embodiments—critical complex optical functions may be performed by one or more photonic integrated circuit(s).
  • An illustrative endoscopic system and structure according to the present disclosure includes an optical receiver selected from the group consisting of spectral domain optical coherence tomography (OCT) receiver, time domain OCT receiver, confocal receiver, fluorescence receiver, and Raman receiver; an endoscope body including fixed distal optics; and a multicore optical fiber optically coupling the fixed distal optics to the receiver.
  • Notably, term endoscope is used throughout the disclosure to describe structures according to the present disclosure. Those skilled in the art will readily appreciate that the disclosure is not specifically limited to endoscopes. More particularly, the disclosure and underlying principles herein are equally applicable to catheters, laparoscopes, imaging guidewires as well as other medical and non-medical devices and structures. Accordingly, when the term endoscope is used, it is intended that it be interchangeable with any instrument or system used to examine the inside of something—oftentimes a body for medical reasons. Such instruments advantageously permit the interior of an organ or other cavity of the body. Of further advantage, endoscopes are capable of being inserted directly into an organ for subsequent examination.
  • BRIEF DESCRIPTION OF THE DRAWING
  • A more complete understanding of the present disclosure may be realized by reference to the accompanying drawings in which:
  • FIG. 1 shows exemplary Prior Art endoscopes;
  • FIG. 2(A), FIG. 2(B) and FIG. 2(C) show a series of exemplary single-mode fiber scanning endoscopes as known in the Prior Art;
  • FIG. 3 shows a schematic diagram of a multi-core fiber endoscope employing an array of swept-source optical coherence tomography (SS-OCT) receivers according to an aspect of the present disclosure;
  • FIG. 4 shows a schematic diagram of a multi-core fiber endoscope employing a single SS-OCT receiver and distinct delays according to an aspect of the present disclosure;
  • FIG. 5 shows a schematic diagram of another multi-core fiber endoscope employing a single SS-OCT receiver and 1:N switch(es) interconnecting the receiver to the endoscope according to an aspect of the present disclosure;
  • FIG. 6 shows a schematic diagram of an illustrative distal portion of a five-core optical fiber endoscope according to an aspect of the present disclosure;
  • FIG. 7(A), FIG. 7(B), FIG. 7(C), FIG. 7(D) and FIG. 7(E) show a series of illustrative arrangements as schematic diagrams other illustrative multi-core fiber endoscope employing: FIG. 7(A) a collimating lens, FIG. 7(B) a fiber/lens coupling element including a passive or active beam steering elements, FIG. 7(C) a graduated index (GRIN) lens or section of multimode fiber, FIG. 7(D) a multi-element collimating lens, and FIG. 7(E) a beam deflector element according to aspects of the present disclosure;
  • FIG. 8 shows a schematic diagram of an illustrative multi-core fiber endoscope wherein the multi-core fiber is connected to a photonic integrated circuit (PIC) according to an aspect of the present disclosure;
  • FIG. 9 show another schematic diagram illustrating a multi-core fiber endoscope wherein the multi-core fiber is connected to a PIC according to an aspect of the present disclosure;
  • FIG. 10 shows yet another schematic diagram illustrating a multi-core fiber endoscope wherein the multi-core fiber is connected to a PIC according to an aspect of the present disclosure;
  • FIG. 11 show a schematic diagram illustrating a multi-core fiber endoscope having a pull-back and/or rotational or twisting proximal motor according to an aspect of the present disclosure;
  • DETAILED DESCRIPTION
  • The following merely illustrates the principles of the disclosure. It will thus be appreciated that those skilled in the art will be able to devise various arrangements which, although not explicitly described or shown herein, embody the principles of the disclosure and are included within its spirit and scope. More particularly, while numerous specific details are set forth, it is understood that embodiments of the disclosure may be practiced without these specific details and in other instances, well-known circuits, structures and techniques have not been shown in order not to obscure the understanding of this disclosure.
  • Furthermore, all examples and conditional language recited herein are principally intended expressly to be only for pedagogical purposes to aid the reader in understanding the principles of the disclosure and the concepts contributed by the inventor(s) to furthering the art, and are to be construed as being without limitation to such specifically recited examples and conditions.
  • Moreover, all statements herein reciting principles, aspects, and embodiments of the disclosure, as well as specific examples thereof, are intended to encompass both structural and functional equivalents thereof. Additionally, it is intended that such equivalents include both currently-known equivalents as well as equivalents developed in the future, i.e., any elements developed that perform the same function, regardless of structure.
  • Thus, for example, it will be appreciated by those skilled in the art that the diagrams herein represent conceptual views of illustrative structures embodying the principles of the invention.
  • In the claims hereof any element expressed as a means for performing a specified function is intended to encompass any way of performing that function including, for example, a) a combination of circuit elements which performs that function or b) software in any form, including, therefore, firmware, microcode or the like, combined with appropriate circuitry for executing that software to perform the function. The invention as defined by such claims resides in the fact that the functionalities provided by the various recited means are combined and brought together in the manner which the claims call for. Applicant thus regards any means which can provide those functionalities as equivalent as those shown herein. Finally, and unless otherwise explicitly specified herein, the drawings are not drawn to scale.
  • Thus, for example, it will be appreciated by those skilled in the art that the diagrams herein represent conceptual views of illustrative structures embodying the principles of the disclosure.
  • By way of some additional background, it is noted that many contemporary imaging endoscopes, catheters, laparoscopes, and imaging guidewires—such as those employed in optical coherence tomography systems—typically employ single mode optical fiber. Such systems perform scanning and imaging by either: 1) spinning the fiber or 2) employing distal optics—for example, motor(s) and actuator(s)—along with a stationary single mode optical fiber. As may be appreciated, configurations such as 1) and 2), above, provide necessary beam deflection(s) to effect the scanning.
  • Turning now to FIG. 1 there is shown several illustrations of contemporary optical endoscopes that are known in the art. While not specifically identified in that Figure, such endoscopes may include an eyepiece, a light post, and an objective assembly. Alternative configurations may include—among other things—an access port for instrument(s) and an “umbilical” connection.
  • FIG. 2(A), FIG. 2(B) and FIG. 2(C) show in schematic form several illustrative examples of single-mode, or multi-mode fiber scanning endoscopes as known in the art. As may be appreciated such endoscopes must be capable of delivering, focusing, scanning and collecting a single spatial-mode optical beam. In addition, the catheter employed oftentimes is flexible—but not always—and has a sufficiently small diameter to facilitate its entry into internal spaces such as arteries. Generally, such endoscopes will include optical control and coupling element(s) at a proximal end, a single-mode fiber running the length of the catheter, and optical focusing and beam directing elements at the distal end. As is generally known by those skilled in the art, the endoscope is configured to scan the beam in a circumferential pattern such that a cross-section image may be made of structure(s) into which it is positioned such as—for example—an artery.
  • As shown in FIG. 2(A), such illustrative examples generally include—at a proximal end—a system 210 which may include light source(s), detector(s) and controlling circuitry and/or operating software(s). Such a system is optically, mechanically, and electrically coupled to a catheter body 230 by a rotary fiber optical joint 220 which includes a spinning optical fiber 231 which in turn is connected—at a distal end—to one or more lens(es) 240 and prism 241 which in turn produces a spatial mode optical beam 250.
  • The illustrative example shown in FIG. 2(B) includes—at its proximal end—system 212, stationary fiber optical joint 213 which is coupled to catheter body 232 and includes a fixed, or stationary, otherwise non spinning single mode optical fiber 233 which in turn is coupled—at the distal end—to one or more lens(es) 242 which in turn is optically coupled to a prism 243 which is spun by distal motor 253.
  • Similarly, the illustrative example shown in FIG. 2(C) includes system 214, stationary fiber optical joint 224, catheter body 234 including stationary single mode optical fiber 235 optically coupled at a distal end to lens(es) 244 and optical phased array(s) 245 thereby producing scanning beam 256.
  • As may be appreciated, spinning optical fibers—such as those employed in configurations such as that in FIG. 2(A), exhibit several disadvantages including non-uniform rotation distortion (NURD), fragility/breakage, cost, reliability, rotational speed limitations along with certain safety considerations that accompany such configurations. Distal motors—such as those employed in FIG. 2(B)—likewise are disadvantaged by cost, size, scanning flexibility, the need for control line(s) and power delivered to the distal end. Distal optical phased arrays—such as those employed in FIG. 2(C)—while offering optimistic promise nevertheless exhibit limitations with respect to image quality, efficiency sidelobes, electrical power requirements and size.
  • Given such noted infirmities with these prior art endoscopes, scanning optical endoscopes exhibiting low cost, small size and acceptable (albeit lower) scanning resolution may be may be constructed according to aspects of the present disclosure. More particularly, and with reference to FIG. 3, there is shown in schematic an illustrative multi-core fiber endoscope 300 according to an aspect of the present disclosure employing an array of swept-source optical coherence tomography (OCT) receivers. As shown in that figure, a multi-core optical fiber is employed and—in sharp contrast to the prior art—no distal mechanical element(s), controllable phased array(s), and/or spinning fibers are used. Of further advantage, individual optical fibers employed may be single-mode fiber(s) or multi-mode fiber(s). It is noted at this point that while specific illustrative examples disclosed herein employ SS-OCT systems and techniques—the disclosure is not so limited. More particularly, other OCT systems and non-OCT systems such as Raman, fluorescence, near-infrared, confocal, and other types of imaging systems that connect similar multicore fiber endoscopes with multicore optical fiber are contemplated and within the scope of this disclosure as well.
  • A multi-core fiber (MCF) has multiple cores positioned within a cladding. Such MCF have been employed in telecommunications applications and shown considerable promise. Advantageously, the number of cores comprising a MCF may differ from application to application—as those individual application needs dictate. By way of illustrative example only—a seven core MCF may have one center and six outer cores. The distance between two neighboring cores is known as the core pitch. By altering the core pitch—it is known by those skilled in the art—that the amount of crosstalk between neighboring cores may be changed.
  • In the illustrative example shown in FIG. 3, a swept-source optical coherence tomography system 310 is coupled to a multi-core optical fiber endoscope 330. As previously noted either single-mode or multi-mode fibers may be employed however for SS-OCT systems such as the one illustrated single-mode fibers are preferably used. Additionally, and as previously noted, while we have shown illustratively an SS-OCT system in this Figure and described in this description, those skilled in the art will readily appreciate that any of a variety of measurement system(s) may be employed and remain consistent with one or more aspect(s) of the present disclosure.
  • As depicted in FIG. 3, a swept source laser 312 is split into N different channels through the effect of splitter 313 or other suitable optical structure(s), each of the N channels optically coupled to a multi-core optical fiber 324 via a proximal end connected (shown in Figure as a dotted line). The N channels are conveyed via the multi-core optical fiber to distal optical structure(s) 370 that may focus light through a transparent, protective cover 360—or transparent windows in a transparent cover—such that output light 380 is conveyed into any external sample, i.e., body tissue(s) or cavities.
  • As will be now understood, light reflected from the sample(s) is collected along the same optical path(s), combined with light directed to a reference arm 315 and interferometrically detected in N separate, opto-electronic receivers 316(1) . . . 316(n), the output of which is directed into a digital signal processing sub-system 317 and other computer(s), controller(s), instrumentation—as necessary (not specifically shown)—for analysis and/or display. Notably, an endoscope such as the one illustrated 330 may include a protective and/or structural jacket 340 to ensure integrity and/or smooth operation/insertion of the device as it is routed through other instruments or directly into a body lumen or other sample environment. Of further note that while this portion of the description has been directed to an SS-OCT type system those skilled in the art will appreciate that systems according to the present disclosure are not so limited. In particular, other types of optical sensing, ranging, or imaging modalities may be employed (e.g., fluorescence, Raman, near-infared spectroscopy, etc.) in systems according to the present disclosure.
  • As may be further appreciated by those skilled in the art, the distal optical structures may advantageously include one or more passive lens assemblies or photonic integrated circuit(s) (PIC). Additionally, planar lightwave circuits (PLC) comprising those optical structures may advantageously be fabricated from InP or Si photonic materials—among others. By employing one or more PICs fabricated from well-known materials using highly evolved fabrication technologies contemporary design tools may be employed to design, simulate and manufacture the distal optical structures while producing benefits related to high precision, small size and low-cost. Still further, such distal optics according to the present disclosure may be fabricated—either in whole or in part—from molded optical materials and components thereby further lowering their cost and manufacturability.
  • Notably, while the distal optics of the system so described may comprise one or more PICs—so may elements of the SS-OCT portion 310 of the system. More particularly, on one illustrative embodiment according to the present disclosure—the SS-OCT portion of the system 310 shown schematically within the dotted line of FIG. 3, (excluding any elements/components not suitable for PIC fabrication presently—i.e., computers, etc.) may comprise one or more PICs such that a compact, robust, low-cost structure(s) result. As those skilled in the art will further appreciate and as will become apparent to those skilled in the art, such PIC fabrication methodologies may advantageously be applied to other designs/configurations according to the present disclosure including those described herein.
  • Of particular interest to those skilled in the art is that while employing a PIC a vertical cavity surface emitting laser (VCSEL) or other laser structure such as verner tuned laser may be integrated into an SS-OCT PIC such that a single PIC includes a VCSEL transmitter, waveguide(s) for beam handling and one or more optical receivers such as a dual-balanced, dual-polarization, I/Q receiver—among other(s). In sharp contrast to contemporary configurations, such PICs may be designed so that VCSEL emission light is coupled into a silicon waveguide.
  • With reference now to FIG. 4, there is shown a schematic of an illustrative embodiment of a multi-core fiber endoscope system 400 employing a single SS-OCT receiver and distinct delay(s) according to an aspect of the present disclosure. As depicted in that Figure, a single receiver 410 is employed and SS-OCT information from each optical fiber comprising the multi-core fiber 425 is extracted through the utilization of distinct delays 414 (D . . . Dn). By employing different delays in each fiber path, information about optical properties from each path is transformed into distinct intermediate frequencies (i.f.) at any photodetector(s) used. Such an approach of encoding two signals into different if. frequencies has been employed in polarization sensitive OCT (PS-OCT) but has not—prior to the present disclosure—been employed in optical endoscopes and in particular not in conjunction with multi-core optical endoscopes according to the present disclosure.
  • As may be appreciated with continued reference to FIG. 4, DSP unit 417 may process these n distinct if. frequencies as they arrive as different—and substantially non-overlapping—frequency bands. Those skilled in the art will readily appreciate that such a configuration results in considerable advantage over the prior art as it utilizes only one receiver and exhibits only a 1/n loss in reflected signal power and transmitted power. Note further that while this illustrative configuration is shown, those skilled in the art will now appreciate from this disclosure that alternative configurations according to the present disclosure may be constructed that achieve the same result(s).
  • Similar to the system shown previously with respect to FIG. 3, the receiver 410 is coupled to the endoscope 430 by the multicore optical fiber 425, wherein each of the individual fibers comprising the multicore optical fiber includes one or more distinct delay elements 414 (D. . . . Dn) which produces a distinct delay for each of the individual fibers. The endoscope 430 generally includes a body—providing a protective and structural jacket 440 to the multicore fiber 425 as well as other elements positioned therein and comprising the overall endoscope 430. Notably, distal optics 470 produce optical scan beams 480 and is generally protected through the effect of cap, 460. As will become apparent to those skilled in the art, a variety of distal optical configurations are contemplated according to the present disclosure.
  • FIG. 5 shows yet another illustrative embodiment of a multi-core optical endoscope system 500 according to the present disclosure wherein an illustrative SS-OCT sub-system 510 is coupled to a multi-core optical fiber endoscope sub-system 530 through the effect of a 1:N switch 524. As depicted in that Figure, the illustrative sub-system 510 inlcudes a number of circulators 514 along with receiver 516 and DSP 518 for receiving and processing return signals from samples illuminated by beams 580 and under examination by endoscope system 500. In a particular illustrative embodiment of the system 500 shown in the Figure, repetition rate of laser 512 may be synchronized to the switching rate of the 1:N switch 524 such that light is transmitted and received substantially during a single frequency sweep (or multiple thereof). In this manner, inefficiencies associated with switching dynamics are incurred during a period when the laser is blanked—at lower power. In this manner, unused portion(s) of the laser frequency sweep is overlapped in time with unusable portions of the switching during switching transients.
  • With this disclosure, those skilled in the art will readily appreciate that this approach has the advantage of higher optical sensitivity as all of the laser light and sample reflected light is coupled to one (or more) of the optical fibers comprising the multi-core optical fiber. As noted previously, other alternative optical systems and components such as spectral-domain OCT, time-domain OCT, confocal systems, fluorescence sensors, Raman sensors and other may be used in place of the SS-OCT system shown illustratively. Of course, the SS-OCT system including the 1:N switch may be constructed using integrated optical technologies—e.g. silicon photonics—to achieve a compact, reliable, low-cost system. Similarly—and as noted previously—these same techniques/structures/methodologies may be employed with any/all of the illustrative examples disclosed herein.
  • Turning now to FIG. 6, there is shown in schematic form another illustrative embodiment (both side and end view(s)) of a distal end of multi-core fiber endoscope 600 according to an aspect of the present disclosure. As may be observed from that Figure, the distal end of the endoscope includes a protective cap 670 and distal optics including collimating lens(es) 673, fold mirrors 672, and substrate 671 coupled to the multi-core fiber, 625 which in this illustrative embodiment includes 5 (five) single optical fibers shown arranged as a central fiber with four perimeter fibers. Of course, those skilled in the art will appreciate that the number of individual fibers and number(s) of individual distal optical elements may be changed as specific application needs dictate. Additionally, the arrangement of the individual fiber(s) and distal optical element(s) may change from application to application as well. Shown further in that Figure is the light beam patters 675 which emanate from the distal optics.
  • With continued reference to FIG. 6—and as will be appreciated by those skilled in the art—certain details of structural and protective jacket (body) of the endoscope is not shown for simplicity. Operationally, light emanating from each fiber core is collected and directed into tissue/structures through the effect(s) of lens(es) 673 and mirrors 672. Notably, while the term “mirrors” is used herein—the disclosure is not so specifically limited. Other optical structures which redirect and/or the light in a desired manner such as prisms, light guides, photonic integrated circuits, etc., are contemplated for such structures and purpose as well.
  • Accordingly, there exist numerous approaches to the distal optics of a multi-core fiber optic endoscope according to the present disclosure. In particular, lens(es) may be graduated index (GRIN) lenses, ball lenses, fiber lenses, and/or lens arrays including multimode, multicore fiber lens that may be affixed or fusion spliced to the distal end of the multi-core fiber. Optional fold mirrors (or prisms or other structures) may be used to redirect light from optical fiber core(s) substantially away from endoscope axis—as desired. Also, one or more center cores may be coupled to optical structures (lenses, etc) that direct light substantially along the endoscope axis.
  • Advantageously, and as will be readily appreciated by those skilled in the art, all distal optical elements—or selected components thereof—may be made from discrete components, one or more molded components, photonic integrated circuit(s) or combinations therof. As shown in the Figure(s), a protective cap may be fully or partially transparent or include windows to allow light to traverse from optical fibers and/or optical elements to/from samples under examination while providing a smooth, sufficiently strong, and appropriately shaped character such that it may be presented/inserted/retrieved from anticipated pathways such as the interior of a bodily lumen. Furthermore—as shown in FIG. 6, the entire distal optics may be assembled and/or fabricated as part of or on top of a substrate. Advantageously, the substrate may allow beam expansion from fiber to lens(es) such that a desired focus, beam waist etc. may be realized. As an illustrative example—and not considered limiting—if a multicore fiber is operating in a single mode regime at 1300 nm, then the core size is ˜9 um. As is known in the art, to a achieve a ˜20 um beam waist (1/ê2) at a ˜1 mm focal length requires ˜28 um diameter (1/ê2) at a face of a lens (in air). Longer focal lengths require a correspondingly larger beam diameter at the lens face where requires a larger lateral separation between fiber cores in the multicore fiber. As may be appreciated, it is desirable that light propagating along the fiber cores and up to and out of any lense(s) does not have substantial leakage from one channel to another.
  • Of further note, alternative illustrative embodiments of the arrangement of FIG. 6 may not necessarily include the lens(es) depicted in that Figure. In particular, one or more fold mirrors may be employed to redirect light into/away from the fiber axes—as appropriate. Advantageously, such a configuration is not only simple, but limited imaging range may be achieved (˜0.3 um the Rayleigh range assuming a 1310 nm wavelength and a ˜9 um beam waist at fiber facet). Accordingly—and as will be readily understood by those skilled in the art—there are a variety of other focal length/focal spot size width exit beam diameter design tradeoffs that may be made depending on the desired operating parameters.
  • As may be appreciated, there are many medical and non-medical applications that would benefit from a simple, low-cost, compact, reusable and/or disposable endoscope such as one(s) constructed according to the present disclosure. Such applications include where a precise, continuous profile of an intimal surface of a lumen is not needed but a measurement of 2, 4, or 8 cross sectional dimensions of the lumen opening is sufficient. For example, when using a nine core optical fiber with one fiber as a central fiber and eight fibers positioned concentrically around the perimeter of that central fiber—each perimeter fiber having a fold mirror associated with it—then four cross-sectional measurements along the 0, 45, 90 and 135 degree axis may be made along with one forward axial measurement. Such measurement(s) may be combined with fiber pull-back mechanism(s) to pull (or push) the endoscope substantially along the axis of the fiber. As will be shown and discussed, it is possible to perform a manual or automated twisting action—back and forth—to sample more of the circumferential area of interest. In this manner four cross-sectional measurements may continuously be made as the endoscope/fiber is pulled back. Such measurement(s) may be useful for a variety of applications including sizing lumens for stents or other therapeutic or interventional procedures. Of further advantage, such endoscope(s) may be combined with other measurement devices/techniques including optical measurements (fluorescence, NIR, Raman) or non-optical devices (e.g., pressure, temperature, pH, etc.) It is also possible to combine such device(s) with therapeutic devices such as surgical lasers, cryo or RF ablation, mechanical cutting tools, and/or other devices/structures. Of distinct advantage, it is possible to position such devices within the inside of a needle—due to its small size.
  • FIG. 7(A), FIG. 7(B), FIG. 7(C), FIG. 7(D) and FIG. 7(E) show a series of illustrative arrangements as schematic diagrams other illustrative multi-core fiber endoscope employing: FIG. 7(A) a collimating lens, FIG. 7(B) a fiber/lens coupling element including a passive or active beam steering elements, FIG. 7(C) a graduated index (GRIN) lens or section of multimode fiber, FIG. 7(D) a multi-element collimating lens, and FIG. 7(E) a beam deflector element—as part of distal optics all according to certain aspects of the present disclosure.
  • More particularly FIG. 7(A) shows another illustrative example of a multi-core fiber endoscope 700 according to the present disclosure wherein a single, shared collimating lens 710 is employed to collimate multiple outputs 715 from multi-core optical fiber 730. Advantageously, the lens may be a single element lens that is coupled to the multi-core fiber 730 via a free-space or solid coupling mechanism(s) 720 including direct fusion splice of a graded index lens constructed of optical fiber or cementing a GRIN lens to the end of the multi-core fiber. Of further advantage, the lens so coupled may be a single element or multiple, separate elements. Such lens(es) may be a GRIN lens, ball lens or aspheric molded glass lens—among other types as well. One additional possibility is the construction of lensing element(s) using fiber gratings within the core or cladding material of the multi-core fiber.
  • With reference now to FIG. 7(B), there is shown yet another illustrative example of a multi-core fiber endoscope 701 according to an aspect of the present disclosure wherein a fiber/lens coupling element 720 includes a passive or active beam steering element(s) 721, i.e., a prism element, to adjust the focus location of light emanating from each of the individual fibers comprising the multi-core fiber (shown emanating onto a collimating lens 710) such that the focus location(s) are nearly identical with respect to any sample(s) being examined.
  • Advantageously, there are a number of approaches to this illustrative example. In particular, if there are N cores in the multi-core fiber then all N cores may be utilized in parallel using receiver structure(s) shown previously. Alternatively, if only a single fiber—for example the center fiber—emits light and the remaining fibers—or a subset of the remaining fibers—may simultaneously be used to collect light reflected from the sample(s). One particular advantage to this approach that will be readily appreciated by those skilled in the art is that beam waists are in the same—but not necessarily exact same) location and additional information about angular scattering and back reflection of light from the sample may be obtained and used to differentiate tissue structure. Of further advantage, using one (or more) of the individual fibers comprising the multi-core optical fiber to illuminate and using other fibers to collect light reflected from the sample(s) may be extended to any of the embodiments contemplated herein or derivatives therof.
  • FIG. 7(C) shows yet another illustrative embodiment of a multi-core optical fiber endoscope 702 according to an aspect of the present disclosure. In particular, a lens employed may advantageously be a GRIN lens or a section of multimode fiber exhibiting a property to image facets of the multi-core fiber at an appropriate distal beam focus. The use of a multimode fiber, as is known in the art, is particularly attractive since it may be fusion spliced or otherwise easily secured to the end of the multicore fiber.
  • As may be appreciated, it is sometimes advantageous to use a section of coreless fiber positioned before the multimode fiber in the optical path to allow beam(s) to more freely expand. Once the beam diameter is of sufficient size to achieve the focal depth and confocal parameter the beam may enter a beam propagation region 735. Once the beam(s) are sufficiently spatially separated an optional distal beam deflector 740 element can be used to deflect some of the beams 742 substantially away from the axis of the endoscope and allow one or more or no beam to pass through substantially uninterrupted to allow for forward ranging 743. The endoscope can have transparent windows at appropriate beam exit locations and as noted previously—when smooth—allows for easier insertion into tight spaces. Similarly, an outer sheath of the endoscope body may be made transparent and constructed from a biocompatible materials. Finally, it is noted that while the particular application of the principles provided in this disclosure have used endoscopes as examples, the disclosure is not so limited. In particular, aspects of this disclosure will apply equally well to using sensors and imaging within catheters, guidewires, needles, laparoscopes and other medical—and non-medical—devices.
  • FIG. 7(D) shows yet another illustrative embodiment of a forward imaging multicore fiber endoscope 703 having a multi-element collimating lens and distal beam deflector element 740. More particularly—and as depicted in that Figure—a multi-element fiber/lens coupling element 720 is employed to individually collect light from each of the individual multicore fiber outputs 715 and direct/focus it such that the light may be more particularly directed onto/into a sample (not specifically shown). In a particular illustrative embodiment, such multi-element fiber/lens coupling element 720 may comprise a multi-mode, multicore optical fiber that is fusion spliced or otherwise connected to a single mode multi-core fiber. In an illustrative embodiment, the outside diameter of the multi-mode multicore fiber is substantially the same as the outside diameter of the single-mode multicore fiber. Of course, other applications may advantageously utilize configurations in which the outer diameters are not the same—for example, those applications in which a larger exit beam diameter is desired.
  • With continued reference to FIG. 7(D), it may be observed that in an illustrative embodiment the multi-mode multi-core fiber is configured with an appropriate GRIN-like profile to achieve appropriate beam parameters for example, focal distance, confocal parameter, etc. for imaging light onto/into the sample (not specifically shown). Additionally, it may be observed that the illustrative embodiment shown in the FIG. 7(E) includes a beam deflector element, that is configured to direct one or more light beams 742 in a direction substantially away from the endoscope axis 751 such that they may be directed to the sample.
  • FIG. 8 shows yet an additional illustrative example according to the present disclosure in which a multicore fiber 810 is coupled to a photonic integrated circuit (PIC—or Integrated Optical Substrate) 820. As will be readily appreciated by those skilled in the art, there exist a wide variety of PIC technologies and materials including PLC, InP and the entire family of Silicon Photonics materials. As depicted in the Figure, light from the multicore fiber 810 is butt coupled to the integrated optic substrate through which it propagates via light guides 830 formed therein, and subsequently impinges on respective surface grating coupler(s) 835. Those skilled in the art will readily understand and appreciate the operation of 1D and 2D surface grating couplers and that any among a variety of same may advantageously be employed in structures according to the present disclosure. Further appreciated, is the fact that the surface grating couplers individually collect diverging light from each of the fibers in the multicore fiber and simultaneously reemit it in such that it is directed into a sample (not shown). Conversely, such surface grating coupler(s) operate in the reverse direction by collecting light from sample(s) and directing it to the fibers comprising the multicore fiber.
  • Turning now to FIG. 9, there is shown an additional illustrative example of multicore optical fiber endoscope distal end 900 according to yet another aspect of the present disclosure. More particularly and as depicted in that Figure, the multicore optical fiber 930 is shown coupled to a photonic integrated circuit 920. As depicted therein, light from the multicore fiber (not specifically shown)—which is butt coupled to the integrated substrate of the PIC 920 wherein it propagates via waveguide structures 925 to one or more surface grating coupler(s) 935. As depicted in this illustrative example, inner grating couplers 935 couple light to/from the waveguides 930 and multicore optical fiber as well as additional waveguides 939 which convey light from inner couplers 935 to/from outer surface grating couplers 937 which emit/receive light to/from sample(s).
  • For simplicity, only a single waveguide is shown connecting optical fibers to respective inner surface grating couplers and subsequently to outer grating couplers. Notably, two or more waveguides may be employed to couple the optical fibers to the inner grating as well as two or more waveguides to couple the inner grating couplers to the outer grating couplers such that one or two polarization modes are conveyed. Note further that the number of waveguides connecting the couplers does not have to be the same for each. As will be appreciated, configurations according to the present disclosure such as that shown in FIG. 9 provide an advantage namely that the radius of the multicore fiber employed may be smaller and still provide a large aperture on emitting surface grating coupler.
  • FIG. 10 shows yet another illustrative example according to the present disclosure of a multicore optical fiber endoscope configuration 1000 wherein the multicore optical fiber 1030 is coupled to a photonic integrated circuit (integrated optical substrate) 1020. Here, the individual cores 1031 of the multicore fiber 1030 are directly butt coupled to a surface grating coupler(s) 1035 fabricated in/on the circuit substrate 1020. The surface grating coupler(s) so coupled to the fibers 1031 are further coupled to respective end facet emitter(s) 1037 via respective optical waveguide(s) 1039. As configured, the end facet emitter(s) 1037 emit light substantially orthogonally to the axis of the multicore fiber (except for a center core). As will be understood and appreciated by those skilled in the art, there exist a number of end facet (horizontal) couplers that may be used including adiabatic coupling approaches. Advantageously—with a configuration such as that depicted—if the wavelength employed is 1300 nm and a focal distance of 2 mm is desired, with a beam waist of ˜20 um, then a beam waist at the exit facet is ˜46 um.
  • At this point it is noted that a number of the illustrative embodiments shown exhibit a central fiber comprising the multicore fiber which is shown in the Figures to emit light along the axis of the fiber (forward). As will be appreciated, such emission—while desirable in certain applications—is not necessary in all. Additionally, it is noted that the individual fibers comprising the multicore fiber do not all have to be the same. In particular, a combination of different fibers may be employed where—for example—some fibers are single mode while others are multimode fibers. Further, some of the fibers may be employed for imaging and sensing while others may be used for invasive or other therapeutic procedures or other diagnostic modalities.
  • As will be appreciated, in many optical systems, including OCT systems, there is a tradeoff made between the measurement range (e.g. the confocal parameter or 2× the Rayleigh Range) and the resolution at the beam waist. Generally, the tighter the beam waist, the higher the lateral resolution but the shorter the measurement range. One of the attractive features of PIC and other integrated optical designs is that by using the high-resolution lithographic techniques for manufacturing the PICs one can make very complex amplitude and/or phase masks in the surface gratings.
  • For example, Bessel beam generation, and other similar depth-of-filed extension techniques, may be designed into the phase mask to provide extended measurement range for a given lateral resolution. Such depth-of-field extension techniques, can be designed into the surface grating couplers using PIC design tools and are advantageously applicable embodiments according to the present disclosure shown and described.
  • As noted previously, one of the advantages of using a multicore fiber is that it allows several simultaneous beams to be guided up/down the endoscope for sensing, imaging, and ranging. One application of such an endoscope acquires several readings of an interior dimensions of a lumen and/or measures properties of interest of the lumen wall. While a single core configuration having a distal motor or a rotating fiber (as is known in SS-OCT cardiovascular and gastroenterology systems) can produce a continuous measurement of a lumen, such an approach comes with noted disadvantages including increased cost, size, and complexity of the endoscopic probe. Multicore fiber configurations according to the present disclosure have the potential to be smaller and therefore be employed into tighter lumens and medical devices (e.g. imaging needles).
  • Of further advantage, it is possible to include additional measurement or imaging capability to multi-core fiber endoscopes constructed according to the present disclosure. Turning now to FIG. 11 there is shown a multicore fiber endoscope 1100 including a pull-back (or push-back) and/or torsional element 1150 Such an element allows for the manual and/or automated pulling-back (or pushing forward) of the distal end of the endoscope along the axis of the endoscope body and lumen in which it is positioned. In this manner, optical measurements may be made along the axis of the lumen which advantageously allows several two-dimensional images to be obtained. Alternatively, and in another illustrative embodiment, the entire multi-core fiber may be rotated back and forth (to and fro) as to radially scan the distal end of the endoscope and therefore the lumen/sample. This advantageously allows additional regions of the sample to be measured. It is also contemplated to have both pullback capability and twisting back and forth capability.
  • Note further that illustrative embodiments according to the present disclosure have depicted a number of ways to image light from a multicore fiber into a sample. There are of course other methods and combinations of the methods shown that may be implemented and are contemplated herein. Additionally, there are also many other aspects of a fiber endoscope design known in the art while not specifically shown and described. Such aspects include protective jackets (metal or plastic), torque cables, markers for x-ray, CT, or MM imaging, etc. With this disclosure and teachings in place, those skilled in the art will readily understand and appreciate that there are numerous applications of structures and techniques according to the present disclosure in addition to SS-OCT and endoscopes including—but not limited to—catheters, guidewires, imaging needles, laparoscopes, and other medical and non-medical devices.
  • At this point those skilled in the art will readily appreciate that while the methods, techniques and structures according to the present disclosure have been described with respect to particular implementations and/or embodiments, those skilled in the art will recognize that the disclosure is not so limited. Accordingly, the scope of the disclosure should only be limited by the claims appended hereto.

Claims (18)

1. An optical endoscope system comprising:
an optical receiver selected from the group consisting of spectral domain optical coherence tomography (OCT) receiver, time domain OCT receiver, confocal receiver, fluorescence receiver, Raman receive, and swept-source optical coherent tomography (SS-OCT) receiver;
an endoscope body including fixed distal optics; and
a multicore optical fiber optically coupling the fixed distal optics to the receiver.
2. The optical endoscope system of claim 1 further comprising N delay elements positioned in an optical path between the receiver and the fixed distal optics.
3. The optical endoscope system of claim 1 further comprising a photonic integrated circuit (PIC) onto which is fabricated the receiver.
4. The optical endoscope system of claim 3 further comprising a vertical cavity surface emitting laser (VCSEL) fabricated onto the PIC with the receiver.
5. The optical endoscope system of claim 4 further comprising a VCSEL transmitter, waveguides for beam handling and one or more optical receivers including a dual-balanced, dual-polarization I/Q receiver.
6. The optical endoscope system of claim 2 wherein said delay elements are configured such that different delays are introduced into different optical fiber paths such that N distinct intermediate frequencies are produced and applied to one or more photodetector(s).
7. The optical endoscope system of claim 6 further comprising a digital signal processor (DSP) for processing the N distinct intermediate frequencies.
8. The optical endoscope system of claim 1 further comprising a 1:N switch interposed between the receiver and the multicore optical fiber and configured such that a repetition rate of a laser comprising the receiver is synchronized to a switching of the 1:N switch.
9. The optical endoscope system of claim 1 wherein said fixed distal optics includes a number of collimating lenses and a number of fold mirrors.
10. The optical endoscope system of claim 1 wherein said fixed distal optics includes a collimating lens configured such that light beams output from the lens diverge.
11. The optical endoscope system of claim 1 wherein said fixed distal optics includes a collimating lens configured such that the light beams output from the lens converge at a common focal point.
12. The optical endoscope system of claim 1 wherein said fixed distal optics includes a fiber/lens coupler, a beam propagation region, and one or more beam deflector elements configured such that a number of optical beams are directed in a direction substantially orthogonal to an axis of the endoscope body.
13. The optical endoscope system of claim 1 wherein said fixed distal optics includes an integrated optical substrate configured such that a number of optical beams are directed in a direction away from an axis of the endoscope body.
14. The optical endoscope system of claim 13 wherein said integrated optical substrate includes a number of surface grating couplers that receive light from the multicore optical fiber and a subset of the number of grating couplers direct the light received in a direction away from an axis of the endoscope body.
15. The optical endoscope system of claim 14 wherein at least one of the couplers receives light from the multicore optical fiber and directs the light received in a direction along the axis of the endoscope body.
16. The optical endoscope system of claim 15 wherein said integrated optical substrate includes a number of optical waveguides which optically couple one or more of the optical fibers comprising the multicore optical fiber to one or more of the couplers.
17. The optical endoscope system of claim 1 further comprising a pull-back device configured to effect a translation of a scan region of the system wherein said translation is along an axis of the endoscope body.
18. The optical endoscope system of claim 1 wherein said fixed distal optics includes an integrated optical substrate configured such that a number of optical beams are directed in a direction away from an axis of the endoscope;
wherein said integrated optical substrate includes a number of surface grating couplers that receive light from the multicore optical fiber and a number of emitting grating couplers that receive light from a respective one of the surface grating couplers via a respective optical waveguide;
wherein said light emitted by the emitting grating couplers is emitted in a direction substantially orthogonal to an axis of the endoscope body;
wherein said integrated optical substrate includes waveguides that couple light from the multicore optical fiber to the surface grating couplers;
wherein the waveguides that couple light from the multicore optical fiber to the surface grating couplers are in a plane that is substantially perpendicular to a plane including the waveguides that couple the surface grating couplers to the emitting couplers.
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Cited By (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20160135892A1 (en) * 2014-11-14 2016-05-19 Ams Research, Llc Surgical laser systems and laser devices
US20170343791A1 (en) * 2016-05-30 2017-11-30 Eric Swanson Few-mode fiber endoscope
CN107941782A (en) * 2017-12-11 2018-04-20 南京航空航天大学 Can endoscopic fiber Raman microprobe and detection device
WO2018143794A1 (en) * 2017-01-31 2018-08-09 Nederlandse Organisatie Voor Toegepast-Natuurwetenschappelijk Onderzoek Tno Methods and instruments for measuring samples in a well plate
EP3388816A1 (en) * 2017-04-11 2018-10-17 Nederlandse Organisatie voor toegepast- natuurwetenschappelijk onderzoek TNO Methods and instruments for measuring samples in a well plate
WO2019106209A1 (en) * 2017-11-30 2019-06-06 Fundació Institut De Ciències Fotòniques Optical endoscope
WO2019224146A1 (en) * 2018-05-22 2019-11-28 Grintech Gmbh Optical arrangement for a spectroscopic imaging method and spectroscopic imaging method
US10627485B2 (en) 2013-06-23 2020-04-21 Eric Swanson Light detection and ranging system with photonic integrated circuit
CN111212592A (en) * 2017-05-12 2020-05-29 周超 Spatial division multiplexing optical coherence tomography using integrated photonic devices
CN111419149A (en) * 2020-03-13 2020-07-17 上海应用技术大学 Multi-mode endoscope and endoscopic imaging system
CN111938583A (en) * 2020-07-20 2020-11-17 南昌大学 Multi-focus large-depth-of-field photoacoustic microscopic imaging method and device
EP3431918B1 (en) * 2017-07-20 2021-03-31 Fogale Nanotech Multichannel confocal sensor and related method for inspecting a sample
WO2021081972A1 (en) * 2019-11-01 2021-05-06 福建师范大学 Endoscopic raman spectroscopy detection device for intracavitary tissue
US20210341668A1 (en) * 2020-05-04 2021-11-04 Eric Swanson Multicore Fiber with Distal Motor
US11256080B2 (en) 2015-05-05 2022-02-22 Eric Swanson Fixed distal optics endoscope employing multicore fiber
US20220058829A1 (en) * 2018-09-12 2022-02-24 Brainlab Ag Intra-operative determination of a focal length of a camera for medical applications
EP3932287A4 (en) * 2019-03-26 2022-04-20 Suzhou Argus Medical Technology Corp Ltd Mla-oct imaging catheter, mla-oct imaging system and mla-oct imaging method
US11397075B2 (en) 2013-06-23 2022-07-26 Eric Swanson Photonic integrated receiver
USD960356S1 (en) * 2020-07-03 2022-08-09 Baylis Medical Company Inc. Piercing stylet with non-contacting distal tip
US20220257314A1 (en) * 2021-02-18 2022-08-18 Biosense Webster (Israel) Ltd. Detection of Balloon Catheter Tissue Contact Using Optical Measurement
US11534058B2 (en) * 2018-05-03 2022-12-27 The General Hospital Corporation Systems, methods, and media for capsule-based multimode endoscopy
US20230070184A1 (en) * 2021-08-23 2023-03-09 Samsung Electronics Co., Ltd. Method for providing image and electronic device supporting the same
EP3706683B1 (en) * 2017-12-12 2023-04-19 Alcon Inc. Multi-core fiber for a multi-spot laser probe
US20230118236A1 (en) * 2021-10-20 2023-04-20 Fujifilm Business Innovation Corp. Collation device and non-transitory computer readable medium storing program
WO2023131040A1 (en) * 2022-01-05 2023-07-13 深圳迈塔兰斯科技有限公司 Endoscope probe, endoscope and scanning control method thereof
US11802759B2 (en) 2020-05-13 2023-10-31 Eric Swanson Integrated photonic chip with coherent receiver and variable optical delay for imaging, sensing, and ranging applications
US11963661B2 (en) * 2022-12-16 2024-04-23 The General Hospital Corporation Systems, methods, and media for capsule-based multimode endoscopy

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10502899B2 (en) * 2013-03-15 2019-12-10 Ideal Industries Lighting Llc Outdoor and/or enclosed structure LED luminaire
US11579366B2 (en) * 2018-12-06 2023-02-14 Optical Engines, Inc. Photonic antenna array with tapered fiber ends
CN114795120A (en) * 2021-11-22 2022-07-29 北京航空航天大学 Multi-modal imaging device

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20110218404A1 (en) * 2009-06-03 2011-09-08 Olympus Medical Systems Corp. Light sensing system and endoscope system
US20120099112A1 (en) * 2010-10-25 2012-04-26 Gerard Argant Alphonse Multi-core low reflection lateral output fiber probe
US20120226118A1 (en) * 2009-09-09 2012-09-06 Delbeke Danae Implantable sensor
US20170205253A1 (en) * 2014-07-25 2017-07-20 Fotech Solutions Limited Distributed Optical Fibre Sensors

Family Cites Families (51)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5041108A (en) * 1981-12-11 1991-08-20 Pillco Limited Partnership Method for laser treatment of body lumens
US6501551B1 (en) 1991-04-29 2002-12-31 Massachusetts Institute Of Technology Fiber optic imaging endoscope interferometer with at least one faraday rotator
US5465147A (en) 1991-04-29 1995-11-07 Massachusetts Institute Of Technology Method and apparatus for acquiring images using a ccd detector array and no transverse scanner
US6485413B1 (en) 1991-04-29 2002-11-26 The General Hospital Corporation Methods and apparatus for forward-directed optical scanning instruments
US5956355A (en) 1991-04-29 1999-09-21 Massachusetts Institute Of Technology Method and apparatus for performing optical measurements using a rapidly frequency-tuned laser
US6564087B1 (en) 1991-04-29 2003-05-13 Massachusetts Institute Of Technology Fiber optic needle probes for optical coherence tomography imaging
US6134003A (en) 1991-04-29 2000-10-17 Massachusetts Institute Of Technology Method and apparatus for performing optical measurements using a fiber optic imaging guidewire, catheter or endoscope
EP0581871B2 (en) 1991-04-29 2009-08-12 Massachusetts Institute Of Technology Apparatus for optical imaging and measurement
US5212743A (en) 1992-02-12 1993-05-18 At&T Bell Laboratories Automatic polarization controller having broadband, reset-free operation
WO1998052021A1 (en) 1997-05-16 1998-11-19 Massachusetts Institute Of Technology Grating based phase control optical delay line
US6137585A (en) 1998-05-15 2000-10-24 Laser Diagnostic Technologies, Inc. Method and apparatus for recording three-dimensional distribution of light backscattering potential in transparent and semi-transparent structures
US6191862B1 (en) 1999-01-20 2001-02-20 Lightlab Imaging, Llc Methods and apparatus for high speed longitudinal scanning in imaging systems
US6445939B1 (en) 1999-08-09 2002-09-03 Lightlab Imaging, Llc Ultra-small optical probes, imaging optics, and methods for using same
US6891984B2 (en) 2002-07-25 2005-05-10 Lightlab Imaging, Llc Scanning miniature optical probes with optical distortion correction and rotational control
EP2030563A3 (en) 2003-06-06 2009-03-25 The General Hospital Corporation Process and apparatus for a wavelength tuning source
US7061618B2 (en) 2003-10-17 2006-06-13 Axsun Technologies, Inc. Integrated spectroscopy system
EP2293031B8 (en) 2003-10-27 2024-03-20 The General Hospital Corporation Method and apparatus for performing optical imaging using frequency-domain interferometry
GB2409033B (en) 2003-12-12 2006-05-24 Lein Applied Diagnostics Ltd Extended focal region measuring apparatus and method
EP2264841B1 (en) 2005-01-20 2016-01-20 Massachusetts Institute of Technology (MIT) Mode locking methods and apparatus
US7530948B2 (en) 2005-02-28 2009-05-12 University Of Washington Tethered capsule endoscope for Barrett's Esophagus screening
EP2275026A1 (en) 2005-09-29 2011-01-19 The General Hospital Corporation Arrangements and methods for providing multimodality microscopic imaging of one or more biological structures
ES2847098T3 (en) 2007-01-10 2021-07-30 Lightlab Imaging Inc Methods and apparatus for scanning source optical coherence tomography
US8463141B2 (en) * 2007-09-14 2013-06-11 Alcatel Lucent Reconstruction and restoration of two polarization components of an optical signal field
US8515221B2 (en) 2010-01-25 2013-08-20 Axsun Technologies, Inc. Silicon optical bench OCT probe for medical imaging
US20110282191A1 (en) 2010-05-13 2011-11-17 Oprobe, Llc Optical coherence tomography for neural-signal applications
US9025158B2 (en) * 2010-06-01 2015-05-05 Intuitive Surgical Operations, Inc. Interferometric measurement with crosstalk suppression
US20120002971A1 (en) 2010-06-30 2012-01-05 Alcatel-Lucent Usa Inc. Polarization-tracking device having a waveguide-grating coupler
EP2616783B1 (en) * 2010-09-17 2021-01-27 Intuitive Surgical Operations Inc. Interferometric measurement system and method for compensating for non-ideal multi-core optical fiber structure
US8854629B2 (en) 2010-11-17 2014-10-07 Finisar Corporation Optical coherence tomography system and method
US8437007B2 (en) 2010-12-30 2013-05-07 Axsun Technologies, Inc. Integrated optical coherence tomography system
US9162404B2 (en) 2011-03-05 2015-10-20 Alcatel Lucent Radial optical coupler
US8947648B2 (en) 2011-03-06 2015-02-03 Ninepoint Medical, Inc. Systems and methods for signal processing in optical imaging systems
US8868356B2 (en) * 2011-03-07 2014-10-21 St. Jude Medical, Inc. Multi-channel optical coherence tomography for imaging and temperature and force sensing
US9008142B2 (en) 2011-07-22 2015-04-14 Insight Photonic Solutions, Inc. System and method for optimization of coherence length of tunable laser sources
US8787708B2 (en) 2011-08-15 2014-07-22 Alcatel Lucent Endless phase shifting
US8665554B2 (en) 2012-01-11 2014-03-04 Oracle International Corporation Ratcheting gripper for a storage library
US9435959B2 (en) 2012-04-26 2016-09-06 Acacia Communications, Inc. Coupling of fiber optics to planar grating couplers
EP2929288A4 (en) 2012-12-06 2016-07-06 Univ Lehigh Space-division multiplexing optical coherence tomography apparatus
US9400169B2 (en) 2012-12-06 2016-07-26 Lehigh University Apparatus and method for space-division multiplexing optical coherence tomography
CN104870930A (en) 2012-12-06 2015-08-26 周超 System and method for parallel imaging optical coherence tomography
US8994954B2 (en) 2012-12-28 2015-03-31 Axsun Technologies, Inc. System and method for stabilizing mode locked swept laser for OCT medical imaging
US9464883B2 (en) 2013-06-23 2016-10-11 Eric Swanson Integrated optical coherence tomography systems and methods
US9683928B2 (en) 2013-06-23 2017-06-20 Eric Swanson Integrated optical system and components utilizing tunable optical sources and coherent detection and phased array for imaging, ranging, sensing, communications and other applications
WO2015168594A1 (en) 2014-05-02 2015-11-05 Massachusetts Institute Of Technology Scanning optical probe
US20160231101A1 (en) 2015-02-06 2016-08-11 Eric Swanson Swept-source optical coherence tomography (ss-oct) system with silicon photonic signal processing element having matched path lengths
US20160357007A1 (en) 2015-05-05 2016-12-08 Eric Swanson Fixed distal optics endoscope employing multicore fiber
US10126572B2 (en) 2016-03-31 2018-11-13 Huawei Technologies Co., Ltd. Automatic endless polarization controller for a silicon-on-insulator platform
US10969571B2 (en) 2016-05-30 2021-04-06 Eric Swanson Few-mode fiber endoscope
US10907951B2 (en) 2016-09-26 2021-02-02 Academisch Medisch Centrum Single-chip optical coherence tomography device
US10401883B2 (en) 2018-01-11 2019-09-03 Eric Swanson Optical probe using multimode optical waveguide and proximal processing
US20210149101A1 (en) 2019-11-14 2021-05-20 Eric Swanson Multicore Fiber Instrument with 3D-Printed Distal Optics

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20110218404A1 (en) * 2009-06-03 2011-09-08 Olympus Medical Systems Corp. Light sensing system and endoscope system
US20120226118A1 (en) * 2009-09-09 2012-09-06 Delbeke Danae Implantable sensor
US20120099112A1 (en) * 2010-10-25 2012-04-26 Gerard Argant Alphonse Multi-core low reflection lateral output fiber probe
US20170205253A1 (en) * 2014-07-25 2017-07-20 Fotech Solutions Limited Distributed Optical Fibre Sensors

Cited By (50)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11579356B2 (en) 2013-06-23 2023-02-14 Eric Swanson Integrated optical system with wavelength tuning and spatial switching
US11243346B2 (en) 2013-06-23 2022-02-08 Eric Swanson Interferometric optical fiber measurement system with multicore optical fiber
US11397075B2 (en) 2013-06-23 2022-07-26 Eric Swanson Photonic integrated receiver
US10895525B2 (en) * 2013-06-23 2021-01-19 Eric Swanson Optical measurement system using multicore optical fiber
US11243347B2 (en) 2013-06-23 2022-02-08 Eric Swanson Optical fiber system with photonic integrated circuit coupled to multicore optical fiber
US10627485B2 (en) 2013-06-23 2020-04-21 Eric Swanson Light detection and ranging system with photonic integrated circuit
US11213351B2 (en) 2014-11-14 2022-01-04 Boston Scientific Scimed, Inc. Surgical laser systems and laser devices
US10219863B2 (en) * 2014-11-14 2019-03-05 Boston Scientific Scimed, Inc. Surgical laser systems and laser devices
US20160135892A1 (en) * 2014-11-14 2016-05-19 Ams Research, Llc Surgical laser systems and laser devices
US11852802B2 (en) 2015-05-05 2023-12-26 Eric Swanson Optical instrument for imaging and sensing using multicore fiber
US11256080B2 (en) 2015-05-05 2022-02-22 Eric Swanson Fixed distal optics endoscope employing multicore fiber
US10969571B2 (en) * 2016-05-30 2021-04-06 Eric Swanson Few-mode fiber endoscope
US11774743B2 (en) 2016-05-30 2023-10-03 Eric Swanson Few-mode optical fiber measurement instrument
US20170343791A1 (en) * 2016-05-30 2017-11-30 Eric Swanson Few-mode fiber endoscope
US11371931B2 (en) * 2017-01-31 2022-06-28 Nederlandse Organisatie Voor Toegepast-Natuurwetenschappelijk Onderzoek Tno Methods and instruments for measuring samples in a well plate
WO2018143794A1 (en) * 2017-01-31 2018-08-09 Nederlandse Organisatie Voor Toegepast-Natuurwetenschappelijk Onderzoek Tno Methods and instruments for measuring samples in a well plate
EP3388816A1 (en) * 2017-04-11 2018-10-17 Nederlandse Organisatie voor toegepast- natuurwetenschappelijk onderzoek TNO Methods and instruments for measuring samples in a well plate
JP2020533570A (en) * 2017-05-12 2020-11-19 チャオ ジョウ Space Division Multiplexing Optical Coheren Tomography Using Integrated Photon Device
EP3634203A4 (en) * 2017-05-12 2021-02-24 Chao Zhou Space division multiplexing optical coherence tomography using an integrated photonic device
US11079214B2 (en) * 2017-05-12 2021-08-03 Lehigh University Space division multiplexing optical coherence tomography using an integrated photonic device
CN111212592A (en) * 2017-05-12 2020-05-29 周超 Spatial division multiplexing optical coherence tomography using integrated photonic devices
EP4289348A3 (en) * 2017-05-12 2024-01-17 Chao Zhou Space division multiplexing optical coherence tomography using an integrated photonic device
JP7170033B2 (en) 2017-05-12 2022-11-11 チャオ ジョウ Spatial division multiplexing optical coherence tomography using an integrated photon device
EP3431918B1 (en) * 2017-07-20 2021-03-31 Fogale Nanotech Multichannel confocal sensor and related method for inspecting a sample
CN111788509A (en) * 2017-11-30 2020-10-16 光子科学研究所基金会 Optical endoscope
JP2021514797A (en) * 2017-11-30 2021-06-17 フンダシオ インスティトゥート デ シエンシィズ フォトニクス Optical endoscope
JP7289845B2 (en) 2017-11-30 2023-06-12 フンダシオ インスティトゥート デ シエンシィズ フォトニクス optical endoscope
WO2019106209A1 (en) * 2017-11-30 2019-06-06 Fundació Institut De Ciències Fotòniques Optical endoscope
CN107941782A (en) * 2017-12-11 2018-04-20 南京航空航天大学 Can endoscopic fiber Raman microprobe and detection device
EP3706683B1 (en) * 2017-12-12 2023-04-19 Alcon Inc. Multi-core fiber for a multi-spot laser probe
US11534058B2 (en) * 2018-05-03 2022-12-27 The General Hospital Corporation Systems, methods, and media for capsule-based multimode endoscopy
US20230117240A1 (en) * 2018-05-03 2023-04-20 The General Hospital Corporation Systems, methods, and media for capsule-based multimode endoscopy
WO2019224146A1 (en) * 2018-05-22 2019-11-28 Grintech Gmbh Optical arrangement for a spectroscopic imaging method and spectroscopic imaging method
US11448551B2 (en) 2018-05-22 2022-09-20 Grintech Gmbh Optical arrangement for a spectroscopic imaging method and spectroscopic imaging method
US20220058829A1 (en) * 2018-09-12 2022-02-24 Brainlab Ag Intra-operative determination of a focal length of a camera for medical applications
US11694363B2 (en) * 2018-09-12 2023-07-04 Brainlab Ag Intra-operative determination of a focal length of a camera for medical applications
EP3932287A4 (en) * 2019-03-26 2022-04-20 Suzhou Argus Medical Technology Corp Ltd Mla-oct imaging catheter, mla-oct imaging system and mla-oct imaging method
WO2021081972A1 (en) * 2019-11-01 2021-05-06 福建师范大学 Endoscopic raman spectroscopy detection device for intracavitary tissue
CN111419149A (en) * 2020-03-13 2020-07-17 上海应用技术大学 Multi-mode endoscope and endoscopic imaging system
US20210341668A1 (en) * 2020-05-04 2021-11-04 Eric Swanson Multicore Fiber with Distal Motor
US11681093B2 (en) * 2020-05-04 2023-06-20 Eric Swanson Multicore fiber with distal motor
US11802759B2 (en) 2020-05-13 2023-10-31 Eric Swanson Integrated photonic chip with coherent receiver and variable optical delay for imaging, sensing, and ranging applications
USD960356S1 (en) * 2020-07-03 2022-08-09 Baylis Medical Company Inc. Piercing stylet with non-contacting distal tip
CN111938583A (en) * 2020-07-20 2020-11-17 南昌大学 Multi-focus large-depth-of-field photoacoustic microscopic imaging method and device
US20220257314A1 (en) * 2021-02-18 2022-08-18 Biosense Webster (Israel) Ltd. Detection of Balloon Catheter Tissue Contact Using Optical Measurement
US11849995B2 (en) * 2021-02-18 2023-12-26 Biosense Webster (Israel) Ltd. Detection of balloon catheter tissue contact using optical measurement
US20230070184A1 (en) * 2021-08-23 2023-03-09 Samsung Electronics Co., Ltd. Method for providing image and electronic device supporting the same
US20230118236A1 (en) * 2021-10-20 2023-04-20 Fujifilm Business Innovation Corp. Collation device and non-transitory computer readable medium storing program
WO2023131040A1 (en) * 2022-01-05 2023-07-13 深圳迈塔兰斯科技有限公司 Endoscope probe, endoscope and scanning control method thereof
US11963661B2 (en) * 2022-12-16 2024-04-23 The General Hospital Corporation Systems, methods, and media for capsule-based multimode endoscopy

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