Devices and methods for conveying and controlling light beams for lensless endo-microscopic imagery
11428924 · 2022-08-30
Assignee
- CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE—CNRS (Paris, FR)
- Ecole Centrale de Marseille (ECM) (Marseilles, FR)
- Université d'Aix-Marseille (AMU) (Marseilles, FR)
Inventors
Cpc classification
A61B1/07
HUMAN NECESSITIES
A61B1/00167
HUMAN NECESSITIES
A61B1/0017
HUMAN NECESSITIES
International classification
G02B23/24
PHYSICS
A61B1/07
HUMAN NECESSITIES
Abstract
According to one aspect, the invention relates to a device for transporting and controlling light beams for endo-microscopic imaging without a lens on the distal side comprising a single-mode optical fibre bundle (40) on the distal side, wherein each single-mode optical fibre is intended to receive an elementary light source and to emit a light beam at a distal end; a single-mode optical fibre section (50) arranged at the distal end of the optical fibre bundle and intended to receive the light beams emitted by the single-mode optical fibres of the optical fibre bundle; an optical phase control device arranged on the side of the proximal end of the single-mode optical fibres. The optical phase control device comprises at least one spatial light modulator (30) adapted to apply a phase shift to each of the elementary beams and control means (60) for controlling the spatial light modulator allowing application of a phase shift to each of the elementary beams to form an illumination beam with a determined phase function at the distal end of the multimode optical fibre section (50).
Claims
1. A device for transporting and controlling light beams for endo-microscopic imaging, comprising: a first light guide comprising a single-mode optical fibre bundle, wherein each single-mode optical fibre is intended to receive an elementary light beam at a proximal end and emit a light beam at a distal end, a second light guide comprising a multimode optical fibre section, arranged at the distal end of the first light guide, wherein said multimode optical fibre is a step-index fibre, wherein the multimode optical fibre section is intended to receive the light beams emitted by the single-mode optical fibres of the single-mode optical fibre bundle, and wherein no lens is located at the distal end of the first light guide; an optical device for phase control arranged on the side of the proximal end of the first light guide comprising: at least one spatial light modulator adapted to apply a phase shift to each of the elementary beams; means of programming the first spatial light modulator allowing application of a phase shift to each of the elementary beams in order to form an illumination beam with a determined phase function at the distal end of the multimode optical fibre.
2. The device for transporting and controlling light pulses according to claim 1, wherein the multimode optical fibre section has a length of between 0.1 mm and 20 mm.
3. The device for transporting and controlling light beams according to claim 1, further comprising an optical system adapted to transport of the light beams emitted by the single-mode optical fibres of the optical fibre bundle to the multimode optical fibre section.
4. The device for transporting and controlling light beams according to claim 1, wherein the first light guide comprises a double-clad multi-core fibre.
5. A endo-microscopic imaging system comprising: a light source for emitting light beams; a device according to claim 1 for transporting and controlling the light beams emitted by said source for forming an illumination beam for illuminating an object with a determined phase function; and a detection channel designed to detect the light reflected by the object and transmitted through the second light guide and subsequently through the first light guide, from their distal end to their proximal end.
6. A method for transporting and controlling light beams for endo-microscopic imaging, comprising: receiving elementary light beams at a proximal end of a bundle of N single-mode optical fibres of a first light guide, wherein each single-mode optical fibre is intended to receive an elementary light beam and emit a light beam at a distal end, receiving the light beams emitted by all the single-mode optical fibres of the optical fibre bundle via a multimode core of a multimode optical fibre section of a second light guide, arranged at the distal end of the first light guide, wherein said multimode optical fibre is a step-index fibre, and wherein no lens is located at the distal end of the first light guide; applying a phase shift to each of the elementary beams, by means of at least one first spatial light modulator arranged on the side of the proximal end of the first light guide, in order to form an illumination beam with a determined phase function at the distal end of the multimode optical fibre section.
7. The method according to claim 6, further comprising a preliminary calibration serving to determine the phase shift to be applied to each of the elementary beams depending on the phase function sought for the illumination beam.
8. The method according to claim 6, wherein application of the phase shift to each of the elementary beams aims to form at the distal end of the multimode optical fibre section a convergent illumination beam at a given distance from an output facet of the multimode optical fibre section, enabling formation of a focal point.
9. The method according to claim 8, wherein application of successive phase shifts to each of the elementary beams allows scanning of said focal point in a plane at said given distance from the output facet of the multimode optical fibre section and/or at different distances from the output facet of the multimode optical fibre section.
10. The method for endo-microscopic imaging without a lens on the distal side, comprising: emission of the light beam; transport and control of the light beams by means of a method as described according to claim 6 for illuminating an object by the illumination beam; detection of the light reflected by the object and transmitted through the second light guide and subsequently through the first light guide, from their distal end to their proximal end.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
(1) Other advantages and characteristics of the invention will appear upon reading the description, illustrated by the figures below:
(2)
(3)
(4)
(5)
(6)
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DETAILED DESCRIPTION
(9) The same references are used to designate identical elements in the figures.
(10)
(11) The endo-microscopic imaging system 200 comprises a light source (not illustrated in
(12) The endo-microscopic imaging system 200 further comprises a device for transporting and controlling the light beams emitted by said light source in order to illuminate the object 101 according to a selected intensity figures, for example a focal point scanned in the field, or other forms, depending on the applications. The device for transporting and controlling the light beams typically comprises a first light guide 40 with a single-mode optical fibre bundle, a second light guide 50 with a multimode optical fibre section, wherein the second light guide 50 is arranged at the distal end of the first light guide, and an optical device for phase control arranged on the side of the proximal end of the first light guide, comprising in particular a spatial light modulator 30.
(13) The device for transporting and controlling the light beams is said to be “lensless”, since it does not have any lens on the distal side, i.e. on the side on which the light beams emerge, with the phase being controlled by the phase control device arranged on the side of a proximal end of the device.
(14) In the rest of the description, it will be simpler to use the term “multimode optical fibre” to refer to the multimode optical fibre section. Furthermore, the second light guide can be formed by the multimode optical fibre section or comprise other elements, for example protective elements, known to those skilled in the art.
(15) The single-mode optical fibre bundle can be formed of set of individual single-mode optical fibres, typically a hundred to a few tens of thousands of fibres, grouped in the form of a bundle of fibres, or may consist of a set of single-mode cores of a multi-core fibre, preferably at least a hundred.
(16) Thus, the first light guide can be formed of the set of individual single-mode optical fibres or comprise other elements, for example protective elements, known to those skilled in the art. The first light guide may also comprise a single-clad or double-clad multi-core fibre and include any other elements useful for producing the guide, such as protective elements, known to those skilled in the art. In the case of a double-clad multi-core fibre, a cladding may be a multimode cladding, adapted to propagate the light flow backscattered by the object.
(17) Advantageously, coupling between the single-mode optical fibres of the single-mode optical fibre bundle is less than −20 dB/m, allowing transport and control of the optical beams over a great length of the fibre bundle, while providing the possibility of compensating inter-core phase shift effects.
(18) The length of the single-mode fibres of the fibre bundle 40 is adapted to the application and more specifically, to the length required for the endomicroscope. Typically, the length of the single-mode fibres of the fibre bundle is between 50 cm and 3 m.
(19) Conversely, the multimode optical fibre section is advantageously selected as short as possible and has for example a length of between 0.1 mm and 20 mm, advantageously of between 0.1 mm and 10 mm. The multimode optical fibre section is short enough in this case to be rigid and long enough to allow jamming of the phase of the propagation modes at the output of the single-mode optical fibre bundle.
(20) The multimode optical fibre may for example be a graded-index fibre or a step-index fibre; in the latter case, jamming of the phase of the propagation modes at the output of the single-mode optical fibre bundle can be achieved by means of a section with a very short length, typically between 0.1 mm and 5 mm.
(21) The multimode optical fibre section can also be intended to form a permanent implant in the case of applications to endoscopic deep brain imaging for example. In the latter case, a longer section of multimode fibre may prove to be of value and consequently use of a graded-index multimode fibre may be appropriate.
(22) The optical phase control device is arranged on the side of the proximal end of the single-mode optical fibre bundle and comprises the spatial light modulator 30 adapted to apply a phase shift to each of the elementary beams B.sub.0i, and a control unit 60 for controlling the spatial light modulator allowing application of a phase shift to each of the elementary beams to impart a determined phase function at the distal end of the multimode optical fibre section. The spatial light modulator 30 may for example include a segmented deformable or membrane mirror, for operation in reflection or in transmission.
(23) According to an exemplary embodiment, the imaging system 200 may also comprise means (not illustrated in
(24) The endo-microscopic imaging system 200 also comprises a detection channel for detecting the light backscattered by the object 101 and transmitted via the multimode fibre and the single-mode optical fibre bundle from their distal end to their proximal end. In the example in
(25)
(26) In the example in
(27) In the examples in
(28) For example, as illustrated in
(29) According to another example, as illustrated in
(30) In both these cases, adjustment of the optical system 71 or the optical system 72 does not need to be perfect, the aim being to facilitate transport of the light beams emitted by the single-mode optical fibres of the optical fibre bundle towards the multimode core of the multimode optical fibre section.
(31)
(32)
(33) In the example chosen in order to illustrate the method of transporting and controlling the light beams, an optical system 72, for example a lens, serves to transport the light beams emitted by the single-mode optical fibres of the optical fibre bundle 40 to the multimode optical fibre bundle 50, as illustrated for example in
(34) As illustrated in
(35) The distribution of the electromagnetic field at the output of the multimode fibre 50 is known as output mode u. By means of the method according to the present description, it is attempted to form the output mode u allowing formation of the illumination beam having the desired phase function and/or associated intensity function at the output of the multimode core of the multimode fibre section 50.
(36) As illustrated in
(37) Other forms of illumination beams can be sought depending on the application. In the case of brain imaging for example, an illumination beam may for example be sought, the shape of which corresponds to that of the elements (neurons) that one wishes to visualise.
(38) Knowledge of the phase shifts to be applied to the light beams B.sub.1i, is derived from a preliminary characterisation of the single-mode optical fibre bundle and the multimode fibre section.
(39) It is for example possible to determine experimentally a complete or partial complex transmission matrix of the assembly formed by the single-mode optical fibre bundle and the multimode fibre section. A complex transmission matrix of an optical system generally expresses the amplitude and phase of the light field in a given plane at the output of the optical system as a function of the amplitude and the phase of the light field in a plane at the input of the optical system. Through knowledge of the transmission matrix, it is possible to characterise the system formed by the single-mode optical fibre bundle and the multimode fibre section assembly in order to determine the phase shift to be applied to each of the elementary light beams B.sub.1i.
(40) Thus, a complex transmission matrix K.sub.i.sup.u can be defined, with an amplitude A.sub.i.sup.u and a phase P.sub.i.sup.u:
(41)
(42) In practice, determination of the matrix K.sub.i.sup.u may be partial and may be limited for example to determination of the matrix P.sub.i.sup.u that essentially governs intensity distribution in the plane of the object (with the amplitude A.sub.i.sup.u playing a marginal role). It is likewise possible to determine the matrix K.sub.i.sup.u incompletely, but this may result in less accuracy in the desired phase function for the illumination beam.
(43) In order to determine the matrix K.sub.i.sup.u of the assembly formed by the single-mode optical fibre bundle and the multimode fibre section, interference methods based on measurements of the interference between the light wave at the multimode optical fibre output and a reference wave can be used. The interference figure is analysed for successive phase shifts applied to each of the elementary fibres or, equivalently, to the reference, allowing determination of the matrix K.sub.i.sup.u. This type of method is described for example in the article by Cizmar et al. in which it is sought to determine the transmission matrix of a multimode optical fibre (see ‘Shaping the light transmission through a multimode optical fibre: complex transformation analysis and applications in biophotonics’ Opt Express 19, 18871-18884 (2011)).
(44) Once the transmission matrix K.sub.i.sup.u has been determined, it can be recorded in the control unit 60 of the spatial light modulator 30, so that a preliminary calibration is not necessary for each implementation of the imaging method. Alternatively, a new calibration can be performed before starting a further imaging process.
(45)
(46) In this example, it is assumed that one is seeking to form focal points at different points in the plane Π.sub.obj positioned at a distance z from the output facet 52 of the multimode optical fibre, as illustrated in
(47) For calibration, a matrix detector, for example a camera, is arranged in the plane of the object Π.sub.obj or in a conjugate plane. Each pixel of the camera has an “output mode” referenced u. The number of output modes u therefore corresponds in this example to the number M of camera pixels. It is sought to determine the phases Φ.sub.i to be applied to the elementary light beams B.sub.1i, in order to achieve maximum intensity of each output mode u.
(48) More specifically, a complex transmission matrix K.sub.i.sup.u can be determined linking the N input modes i and the M output modes u:
B.sub.3.sup.u=1,M=K.sub.i.sup.uB.sub.1.sup.i=1,N
(49) The number N of input modes is limited by the number of single-mode optical fibres in the fibre bundle 40 and the number M of output modes is limited by the number of camera pixels.
(50) As explained above, the complex transmission matrix K.sub.i.sup.u can be defined, with an amplitude A.sub.i.sup.u and a phase P.sub.i.sup.u:
(51)
(52) In practice, determination of the matrix K.sub.i.sup.u is solely a matter of measuring the matrix P.sub.i.sup.u that essentially controls the intensity distribution in the plane of the object.
(53) Determination of the matrix P.sub.i.sup.u may comprise the following stages:
(54) Sending two input modes: a reference mode i=0 and an input mode i to which a phase Φ.sub.i is added;
(55) Recording for each output mode u, i.e. for each camera pixel, the resulting intensity for a given number of intensity values equidistant from Φ.sub.i, for example 8, between 0 and 2π, as shown in
(56) Recording for each output mode u of the phase Φ.sub.i which achieves maximum intensity (
(57) Reiteration for each input mode i.
(58) The stages of calibrating the method of transporting and controlling the light beams described above may of course also be applied when the single-mode optical fibre bundle 40 and the multimode fibre section 50 are arranged differently.
(59) In particular, if the input facet 51 is in the same plane, or in a conjugate plane with the output facet 42 of the single-mode fibre bundle 40, the intermediate facet associated with the input facet 51 of the multimode fibre 50 may be indexed in real space (x, y).
(60)
(61) The experimental assembly comprises a laser source 10 emitting a light beam sent on a “wavefront shaper” 503, for example a microlens array or a two-dimensional spatial light modulator drawing a network of quadratic phases simulating a microlens array and forming a set of elementary beams focused on the segments of a segmented deformable mirror 30. A telescope 504, 506 is used to adjust the dimensions of the beam in the plane of the deformable mirror 30. Each segment of the deformable mirror 30 is imaged on a single mode fibre of the single-mode optical fibre bundle 40 (imager 508, 513, 515, 516). A control device 60 for controlling the deformable mirror 30 serves to control the phase Φ.sub.i associated with each input mode i and corresponding to each of the elementary beams. A lens with a focal length of f=500 μm (not visible in
(62) A calibration of the method of transporting and controlling the light beams implemented using the experimental assembly in
(63) In the example shown in
(64) In
(65) Thus, the applicants have shown both theoretically and experimentally that after a very short propagation distance in the core of the multimode fibre, typically 1 mm or a few millimetres depending on the type of fibre, the propagation modes display random phases. This random nature of the phases associated with each propagation mode of the multimode fibre is at the very origin of disappearance of the replicas. Since the relative phase shifts between the modes of the multimode fibre result from the propagation, it will be understood why a step-index multimode fibre is more effective than a graded-index multimode fibre in jamming the modes; indeed, in a step-index fibre, the propagation constants associated with each of the modes are more dispersed, resulting in larger differential phase shifts.
(66) Although the phases accumulated by the different modes during propagation in the multimode fibre are ultimately random, they are however deterministic and are included in determination of the transmission matrix encompassing the first light guide and the multimode optical fibre.
(67) The applicants have thus demonstrated the feasibility of a device for transporting and controlling light beams for lensless endo-microscopy, wherein a function of scanning the field of the object at a given distance z from the output facet 52 of the multimode optical fibre section 50 can be obtained by controlling the phase shifts applied by means of the spatial light modulator 30.
(68) The device for transporting and controlling light beams according to the present description also allows selection of the distance z from the plane of the object. For this purpose, a calibration as described above can be performed for a set of values z of the distance between the plane of the object and the output facet 52 of the multimode optical fibre section.
(69)
(70) More specifically, the light source used to obtain these images is a Titanium:Sapphire laser at 800 nm emitting pulses of 200 fs; the images obtained are two-photon images and the detector 20 is an avalanche photodiode.
(71) These experimental results therefore also demonstrate the application of the method of transporting and controlling light beams in non-linear imaging, since the device is suitable for transmission of short pulses.
(72) However, when handling ultra-short pulses, the device for transporting and controlling light beams according to the present description may also comprise a group delay control device for the light pulses in the single-mode optical fibre bundle, as described in the publication by E. R. Andresen et al. (“Measurement and compensation of residual group delay in a multi-core fibre for lensless endoscopy”, JOSA B, Vol. 32, No. 6, 1221-1228 (2015)).
(73) It is therefore possible to perform lensless endo-microscopic imaging by means of the method described. Apart from transporting and controlling the light beams by means of the method previously described, the endo-microscopic imaging method may also comprise detection of the light backscattered by the object and transmitted via the multimode fibre and the single-mode optical fibre bundle from their distal end to their proximal end.
(74) Although described though a number of detailed exemplary embodiments, the device for transporting and controlling light pulses for so-called “lensless” endo-microscopic imaging, in addition to the lensless endo-microscopic systems and methods comprise different alternative embodiments, modifications and improvements which will be obvious to those skilled in the art, its being understood that these different alternative embodiments, modifications and improvements fall within the scope of the invention as defined in the following claims.