WO2022209349A1 - Dispositif d'éclairage pour dispositif d'observation, dispositif d'observation et système d'observation - Google Patents

Dispositif d'éclairage pour dispositif d'observation, dispositif d'observation et système d'observation Download PDF

Info

Publication number
WO2022209349A1
WO2022209349A1 PCT/JP2022/005575 JP2022005575W WO2022209349A1 WO 2022209349 A1 WO2022209349 A1 WO 2022209349A1 JP 2022005575 W JP2022005575 W JP 2022005575W WO 2022209349 A1 WO2022209349 A1 WO 2022209349A1
Authority
WO
WIPO (PCT)
Prior art keywords
light emitting
light
emitting elements
observation
illumination device
Prior art date
Application number
PCT/JP2022/005575
Other languages
English (en)
Japanese (ja)
Inventor
智之 大木
哲晃 岩根
聡史 長江
Original Assignee
ソニーグループ株式会社
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by ソニーグループ株式会社 filed Critical ソニーグループ株式会社
Publication of WO2022209349A1 publication Critical patent/WO2022209349A1/fr

Links

Images

Classifications

    • G—PHYSICS
    • G02—OPTICS
    • G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B21/00—Microscopes
    • G02B21/06—Means for illuminating specimens
    • G—PHYSICS
    • G02—OPTICS
    • G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B5/00—Optical elements other than lenses
    • G02B5/20—Filters

Definitions

  • the present disclosure relates to an illumination device for an observation device, an observation device, and an observation system.
  • Lamp light sources (halogen lamps and xenon lamps) were widely used as illumination devices for microscopes used to observe pathological specimens due to their good color rendering properties and high brightness. However, since such a lamp light source has a short life and thus requires a running cost, a white LED (Light Emitting Diode) light source has come to be used in recent years.
  • a white LED Light Emitting Diode
  • an illumination device for an observation device that can ensure uniformity in the plane of the observation area and uniformity in the angular space while maintaining high color rendering properties and high luminance.
  • a light source including a housing, a plurality of light emitting elements mounted on the bottom surface of the housing, and a phosphor layer provided above the plurality of light emitting elements; and an optical system for condensing light, wherein the FWHM angle of each light emitting element is ⁇ , the length of one side of the light emitting element is d, and the maximum distance between the adjacent light emitting elements is P.
  • np the refractive index of the medium in the housing
  • T the film thickness of the phosphor layer
  • T the refractive index of the phosphor layer
  • an illumination device that irradiates light and an objective lens that magnifies a sample
  • the illumination device includes a housing, a plurality of light emitting elements mounted on the bottom surface of the housing, and the a light source having a phosphor layer provided above a plurality of light emitting elements; and an optical system for condensing light from the light source, wherein the FWHM angle of each light emitting element is ⁇ , and the light emission
  • d be the length of one side of the element
  • P be the maximum distance between the adjacent light emitting elements
  • L the distance between the light emitting element and the phosphor layer
  • the plurality of light emitting elements are provided so as to satisfy the following formula (1):
  • a viewing device is provided.
  • an observation device that observes a biological sample, and a computer that controls the observation device and processes signals obtained from the observation device
  • the observation device includes an illumination device that emits light.
  • an imaging unit configured by an imaging device for imaging the biological sample
  • the lighting device includes a housing, a plurality of light emitting elements mounted on the bottom surface of the housing, and the plurality of light emitting elements.
  • a light source having a phosphor layer provided above Let d be the depth, P be the maximum distance between the light emitting elements adjacent to each other, L be the distance between the light emitting element and the phosphor layer, n be the refractive index of the medium in the housing, and An observation system is provided in which the plurality of light emitting elements are provided so as to satisfy the following formula (1), where T is the thickness of the phosphor layer and np is the refractive index of the phosphor layer. .
  • FIG. 1 is a block diagram showing a configuration example of an observation system 10 according to an embodiment of the present disclosure
  • FIG. FIG. 10 is a diagram showing a configuration example of an illumination unit 102a according to a comparative example
  • FIG. 5 is a diagram showing a configuration example of a light source 500a according to a comparative example
  • FIG. 5 is a diagram showing a simulation result of luminance distribution of a light source 500a according to a comparative example
  • FIG. 5 is a diagram showing a radiation intensity distribution of light emitted from a light emitting element 522 according to an embodiment of the present disclosure
  • 1 is a diagram (part 1) illustrating a configuration example of a light source 500 according to an embodiment of the present disclosure
  • FIG. 2 is a diagram (Part 2) showing a configuration example of a light source 500 according to an embodiment of the present disclosure
  • 3 is a diagram illustrating a configuration example of an illumination unit 102 according to an embodiment of the present disclosure
  • FIG. FIG. 11 is a diagram (Part 1) showing a simulation result of the luminance distribution of the light source 500 according to the embodiment of the present disclosure
  • FIG. 10 is a diagram (Part 2) showing a simulation result of the luminance distribution of the light source 500 according to the embodiment of the present disclosure
  • It is a figure which shows roughly the whole structure of a microscope system.
  • It is a figure which shows the example of an imaging system.
  • It is a figure which shows the example of an imaging system.
  • 1 is a block diagram showing an example of a schematic configuration of a diagnostic support system
  • a tissue section or cell that is part of a tissue obtained from a living body (eg, human body, plant, etc.) is referred to as a biological sample.
  • the biological sample described below may be subjected to various staining as necessary.
  • the biological sample does not have to be dyed in various ways.
  • staining includes not only general staining represented by HE (hematoxylin-eosin) staining, Giemsa staining or Papanicolaou staining, but also periodic acid-Schiff (PAS) staining used when focusing on a specific tissue. and fluorescent staining such as FISH (Fluorescence In-Situ Hybridization) and enzyme antibody method.
  • FIG. 1 is a block diagram showing a configuration example of an observation system 10 according to an embodiment of the present disclosure.
  • the observation system 10 according to this embodiment is a scanner system that digitally photographs a slide 300 on which a biological sample (for example, cell tissue or the like) is mounted.
  • a biological sample for example, cell tissue or the like
  • an observation system 10 can include a scanner (observation device) 100 and an image processing device 200 .
  • the scanner 100 and the image processing apparatus 200 may be communicatively connected to each other via various wired or wireless communication networks.
  • the number of scanners 100 and image processing devices 200 included in the observation system 10 according to the present embodiment is not limited to the number illustrated in FIG. 1, and may include more.
  • the observation system 10 according to this embodiment may include other servers, devices, and the like (not shown). Below, an outline of each device included in the observation system 10 according to the present embodiment will be described.
  • the scanner 100 irradiates the slide 300 of the biological sample placed on the stage 108 of the scanner 100 with predetermined illumination light, and emits light transmitted through the slide 300 or light emitted from the slide 300. can be photographed (imaged).
  • the scanner 100 can be a microscope including a magnifying glass (not shown) and a digital camera (not shown) that can magnify and photograph a biological sample.
  • the scanner 100 may be implemented by any device having a photographing function, such as a smartphone, tablet, game machine, or wearable device.
  • the scanner 100 is driven and controlled by an image processing device 200, which will be described later, and the image captured by the scanner 100 is stored in the image processing device 200, for example. A detailed configuration of the scanner 100 will be described later.
  • the image processing device 200 is a device having a function of controlling the scanner 100 and processing an image (signal) captured by the scanner 100 . Specifically, the image processing apparatus 200 controls the scanner 100 to capture a digital image of the biological sample, and performs predetermined image processing on the obtained digital image.
  • the image processing device 200 is realized by any device having a control function and an image processing function, such as a PC (Personal Computer), a tablet, a smartphone, or the like.
  • the image processing device 200 performs stitching processing on a plurality of images to generate a wide-area image, or performs machine learning using the acquired images as teacher data to generate a learning model. good.
  • the image processing apparatus 200 may use the learning model generated in this way to perform estimation, diagnosis, and the like.
  • the scanner 100 and the image processing device 200 may be integrated devices, that is, they may not be realized by a single device. Further, in this embodiment, the scanner 100 and the image processing apparatus 200 described above may be realized by a plurality of devices that are connected via various wired or wireless communication networks and cooperate with each other. Furthermore, the image processing apparatus 200 described above can be realized by, for example, a hardware configuration of a computer described later.
  • the scanner 100 can mainly have an illumination section 102, a sensor section (imaging section) 104, a control section 106, and a stage . Each functional block of the scanner 100 will be sequentially described below.
  • the illumination unit 102 is provided on the side of the stage 108 opposite to the slide placement surface on which the slide 300 can be placed, and irradiates the slide 300 of the biological sample with illumination light under the control of the control unit 106, which will be described later. It is a lighting device that can Also, the illumination unit 102 may have, for example, a lens (optical system) (not shown) that collects the illumination light emitted from the illumination unit 102 and guides it to the slide 300 on the stage 108 . A detailed configuration of the illumination unit 102 will be described later.
  • the sensor unit 104 is provided on the side of the slide arrangement surface of the stage 108, and is a color sensor that detects, for example, red (R), green (G), and blue (B) light, which are the three primary colors. More specifically, the sensor unit 104 can have, for example, an objective lens (not shown) and an imaging element (not shown). Then, the sensor unit 104 can digitally photograph (image) the biological sample and output the photographed digital image to the image processing apparatus 200 under the control of the control unit 106 to be described later.
  • the objective lens (not shown) is provided on the side of the slide arrangement surface of the stage 108, and makes it possible to magnify and photograph the biological sample. That is, the transmitted light transmitted through the slide 300 arranged on the stage 108 is condensed by the objective lens, and the imaging element (illustrated omitted).
  • the imaging device (not shown) has a photographing range having a predetermined horizontal width and vertical width on the slide arrangement surface of the stage 108 according to the pixel size of the imaging device and the magnification of the objective lens (not shown). An image is formed.
  • the imaging range described above is sufficiently narrower than the imaging range of the imaging element.
  • the imaging element can be realized by an imaging element such as a CCD (Charge Coupled Device) or a CMOS (Complementary Metal Oxide Semiconductor).
  • the sensor unit 104 may directly photograph the biological sample without using an objective lens or the like, or may photograph the biological sample via an objective lens or the like, and is not particularly limited. do not have.
  • the control unit 106 can comprehensively control the operation of the scanner 100, and includes processing circuits realized by, for example, a CPU (Central Processing Unit), a ROM (Read Only Memory), a RAM (Random Access Memory), and the like. .
  • the control unit 106 can control the lighting unit 102 and the sensor unit 104 described above. Further, the controller 106 may control a stage drive mechanism (not shown) that moves the stage 108 in various directions.
  • control unit 106 may control the number of shots N and the shooting time of the sensor unit 104 according to commands output from the image processing device 200 . More specifically, the control unit 106 may control the sensor unit 104 to intermittently perform imaging N times at predetermined intervals. Also, the control unit 106 may control the wavelength, irradiation intensity, or irradiation time of the illumination light emitted from the illumination unit 102 . Furthermore, the control unit 106 controls a stage drive mechanism (not shown) that moves the stage 108 in various directions according to the region of interest so that a preset region of interest (ROI) is imaged. good too.
  • ROI region of interest
  • region of interest as used herein means a region (target region) of a biological sample that a user pays attention to for analysis or the like.
  • the stage 108 is a mounting table on which the slide 300 is mounted. Further, the stage 108 may be provided with a stage drive mechanism (not shown) for moving the stage 108 in various directions. For example, by controlling the stage drive mechanism, the stage 108 is freely moved in a direction parallel to the slide arrangement surface (X-axis-Y-axis direction) and in a direction orthogonal to the slide arrangement surface (Z-axis direction). be able to. Further, in this embodiment, the stage 108 may be provided with a sample transport device (not shown) that transports the slide 300 to the stage 108 . By providing such a transport device, the slide 300 to be photographed can be automatically placed on the stage 108, and the replacement of the slide 300 can be automated.
  • FIG. 2 is a diagram showing a configuration example of a lighting unit 102a according to a comparative example
  • FIG. 3 is a diagram showing a configuration example of a light source 500a according to a comparative example
  • FIG. It is a figure which shows the simulation result of luminance distribution.
  • the comparative example shall mean the lighting section and the light source which were studied repeatedly before the present inventors made the embodiment of the present disclosure.
  • a pathological diagnosis method for definitive diagnosis of a disease a method has been proposed in which a pathological specimen is imaged by the scanner 100, the image is digitized and displayed, and the image is referred to for pathological diagnosis. It is In such a situation, in order to ensure that the information necessary for diagnosis is not overlooked in order to make an appropriate pathological diagnosis, the entire observation area of the pathological specimen is given a light spectrum with high color rendering (for example, a Color Rendering Index ( There is a demand for an illumination unit (illumination device) capable of uniformly emitting bright light having a CRI of 90 or higher.
  • illumination unit illumination device
  • the uniformity in the plane of the observation area (the in-plane distribution of the light image reflected when the screen is placed in the observation area must be uniform) and the angle space. Uniformity (that the peak shape of the radiation angle distribution of the light irradiated to the observation area is close to the Lambertian distribution) is required to be ensured.
  • the Lambertian distribution is the light intensity distribution when the luminance of the light-emitting surface of the light-emitting body that emits light is constant regardless of the viewing angle. is proportional to the cosine of the angle formed by and the emitted light.
  • lamp light sources halogen lamps and xenon lamps
  • halogen lamps and xenon lamps have been widely used as light sources for microscopes used to observe pathological specimens due to their good color rendering properties and high brightness.
  • a lamp light source has a short life and thus requires high running costs. Therefore, in recent years, white LED light sources have come to be used.
  • white LED light sources have a longer life than lamp light sources, those with good color rendering have low luminance. Therefore, in the prior art, the number of LED elements (light emitting elements) used in the LED light source is increased to increase the brightness, and the types of phosphors are increased to improve the color rendering properties.
  • color rendering is a very important factor in pathological diagnosis, as it is directly linked to how it looks in pathological diagnosis, which has been cultivated with conventional lamp light sources.
  • Color rendering refers to the properties of a lighting device, etc., that affect how the color of an object appears when the lighting device, etc. irradiates light onto the object. It is said that it is preferable to be close to the direction. More specifically, the color rendering property is indicated by an index called CRI.
  • CRI is 100 in sunlight, and CRI approaches 100 as the appearance of an object is closer to that in sunlight.
  • the illumination unit 102a according to the comparative example includes an optical system 400a including a plurality of lenses 402 and the like, and a light source 500a. Details of each block of the illumination unit 102a according to the comparative example will be described below.
  • optical system 400a The optical system 400a, as shown in FIG. 2, is a Koehler illumination composed of lenses 402a, 402b, 402c, a field stop 412, and an aperture stop 414, and is further diffused to illuminate more uniform light. Includes plate 420 .
  • the focus of the condenser lens passes through the condenser lens (lens 402a in FIG. 2) and the relay lens (lens 402b in FIG. 2) to the light source (
  • the condenser lens, condenser lens, and relay lens are arranged so as to coincide with the point where the image of the light source 500) is formed, and furthermore, the aperture stop 414 is arranged at the coincident point.
  • the condenser lens and the relay lens are arranged so that the focal point of the relay lens coincides with the point where the image of the object is formed through the condenser lens, and the field stop 412 is arranged between the condenser lens and the relay lens. be done.
  • Such Koehler illumination not only irradiates uniform light but also does not directly irradiate the light from the light source, so the distance between the subject and the light source can be increased. The impact can be suppressed. Further, in Koehler illumination, the magnification can be adjusted by adjusting the lens or the like, so the light source can be made small.
  • a diffuser plate 420 is provided above the lens 402a and can make the light uniform by diffusing it.
  • a field stop 412 is provided above the diffusion plate 420 and can adjust the illumination range. Furthermore, since the field stop 412 cuts unnecessary light, it is possible to suppress the occurrence of flare, ghost, etc., and obtain a clear field of view.
  • the lens 402b is provided above the field stop 412 and can converge the substantially parallel light.
  • An aperture stop 414 is provided above the lens 402b and can adjust the brightness.
  • the lens 402c is provided above the aperture stop 414, and can make the condensed light into substantially parallel light again.
  • a diffusion plate 420 is provided in order to obtain uniform light.
  • the optical system 400a of the comparative example is not limited to the Kohler illumination as described above, and may be a critical illumination that does not include the condenser lens 402c.
  • the light source 500a is an illumination device that emits white light or single light. Specifically, as shown in FIG. 3, the light source 500a has a housing 510, a plurality of light emitting elements (eg, LED chips) 522, and a phosphor layer 524. As shown in FIG.
  • the housing 510 has an opening at the top (referred to as an opening surface 510b in the following description), and a plurality of light emitting elements 522 are arranged on the inner side of a bottom surface (substrate) 510a facing the opening surface 510b. is mounted.
  • the light emitting element 522 is a diode that emits light when a voltage is applied, and includes an electrode (not shown) provided on a semiconductor substrate (not shown), a light emitting layer (not shown), and the like.
  • the light source 500a preferably has a plurality of light emitting elements 522 to enhance brightness.
  • the phosphor layer 524 is provided above the plurality of light emitting elements 522, and can absorb light from the light emitting elements 522 and emit light in different wavelength ranges.
  • the phosphor layer 524 contains one or more kinds of phosphors, and preferably contains plural kinds of phosphors in order to improve the color rendering properties.
  • a plurality of types of phosphors emit light in different wavelength ranges.
  • the light emitted from the plurality of light emitting elements 522 and the light emitted from the phosphor layer 524 by absorbing the light from the light emitting elements 522 are provided to face the bottom surface 510a.
  • the light is emitted to the outside of the housing 510 through the opening surface 510b. That is, it can be said that the opening surface 510b is the light emitting surface of the light source 500a.
  • the phosphor layer 524 contains various phosphors in order to improve the color rendering properties of the light source 500a.
  • various phosphors are included, the luminance of the light source 500a is lowered. Therefore, in the comparative example, the number of light emitting elements 522 is increased or the chip size of the light emitting elements 522 is increased in order to suppress the decrease in luminance.
  • the film thickness of the phosphor layer 524 is reduced and the distance between the phosphor layer 524 and the light emitting element 522 is shortened in order to downsize the light source 500a. Due to such miniaturization as well, as can be seen from the simulation result of the luminance distribution on the light emitting surface (opening surface 510b) of the light source 500a shown in FIG. show.
  • the luminance peaks corresponding to the number of light emitting elements 522 occur, so the luminance distribution on the light emitting surface of the light source 500a becomes uneven.
  • the illumination unit 102a it becomes difficult for the illumination unit 102a to ensure uniformity in the plane of the observation area and uniformity in angular space.
  • the diffuser plate 420 is used in the optical system 400a in order to improve the nonuniformity of the luminance distribution of the light source 500a, but the improvement effect of the diffuser plate 420 is limited.
  • the present inventors diligently studied the light source 500 in such a situation, and paid attention to the relationship between the light emitting element 522 and the phosphor layer 524.
  • the details of the embodiments of the present disclosure created by the present inventors will be sequentially described.
  • FIG. 5 is a diagram showing the radiation intensity distribution (radiation angle) of light emitted from the light emitting element 522 according to this embodiment
  • FIGS. 6 and 7 show configuration examples of the light source 500 according to this embodiment. It is a diagram. Specifically, the upper part of FIG. 6 shows a plan view of the light source 500, and the lower part of FIG. 6 shows a cross section of the light source 500 taken along line AA' shown in the upper part. Furthermore, FIG. 7 shows a part of the cross section of the light source 500 and information such as the positional relationship and length of each element.
  • the light distribution characteristic of the light emitted from the light emitting element 522 used has a distribution as shown in FIG.
  • the light source 500 is a lighting device that emits white light or single light, and includes a housing 510 and a plurality of light emitting elements. It has an (LED chip) 522 and a phosphor layer 524 .
  • the housing 510 has an open top (referred to as an open surface 510b), and a plurality of light emitting elements 522 are mounted on the inside of a bottom surface (substrate) 510a facing the open surface 510b.
  • the light-emitting element 522 is a light-emitting diode or laser diode that emits light when a voltage is applied, and has an intensity distribution (radiation angle) of emitted light as shown in FIG. 5, as described above.
  • the light emitting element 522 consists of an electrode (not shown) and a light emitting layer (not shown) provided on a semiconductor substrate (not shown), and here the length of one side is d (see FIG. 7 ).
  • five light emitting elements 522 are arranged on the bottom surface 510a.
  • the number of light emitting elements 522 is not limited to five, and may be plural.
  • the plurality of light emitting elements 522 are preferably arranged so as to be point-symmetrical with respect to the center of the bottom surface 510a, and further arranged so as to satisfy the conditions described later. becomes.
  • the maximum distance between the light emitting elements 522 adjacent to each other is defined as P, and the medium 512 (for example, air) filled between the light emitting elements 522 and the phosphor layer 524 in the housing 510 is Let n be the refractive index of (see Fig. 7).
  • the phosphor layer 524 is provided above the plurality of light emitting elements 522, absorbs light from the light emitting elements 522, and emits light in different wavelength ranges, as shown in the lower part of FIG. be able to. Furthermore, the phosphor layer 524 preferably contains at least one kind of phosphor and further contains plural kinds of phosphors in order to improve the color rendering properties. The multiple types of phosphors emit light in different wavelength bands. In this embodiment, the distance between the light emitting element 522 and the phosphor layer 524 is L, the film thickness of the phosphor layer 524 is T, and the refractive index is np (see FIG. 7).
  • the light emitted from the plurality of light emitting elements 522 and the light emitted from the light emitting elements 522 are absorbed so that the light emitted from the phosphor layer 524 is absorbed by the housing 510 .
  • An opening surface 510b is provided to face the bottom surface 510a in order to emit the light to the outside. That is, it can be said that the opening surface 510b is the light emitting surface of the light source 500 as in the comparative example.
  • a light distribution range ( A plurality of light emitting elements 522 are mounted on the bottom surface 510a such that a portion of the FWHM (1/4) overlaps each other. That is, in this embodiment, by satisfying the following conditions, the light distribution ranges of the light emitting elements 522 can partially overlap each other on the light emitting surface (opening surface 510b).
  • the FWHM of the radiation intensity of each light emitting element 522 is ⁇
  • the length of one side of each light emitting element 522 is d
  • the adjacent light emitting elements 522 Let P be the maximum value of the interval, L be the distance between the light emitting element 522 and the phosphor layer 524, n be the refractive index of the medium 512 in the housing 510, and T be the film thickness of the phosphor layer 524.
  • the refractive index of the phosphor layer 524 is np .
  • the light distribution ranges of the light emitting elements 522 partly overlap each other on the light emitting surface (opening surface 510b). (light distribution), as a result, the luminance distribution on the light emitting surface of the light source 500 can be made uniform.
  • ⁇ is preferably larger than (1/10) ⁇ from the limitation on the interval between the light emitting elements 522, and is smaller than (1/2) ⁇ due to the film thickness T of the phosphor layer 524. is preferred.
  • ⁇ is larger than (1/5) ⁇ and smaller than (1/3) ⁇ . more preferred. In simulations and experiments, good results were obtained when ⁇ was (1/4) ⁇ .
  • the relationship between the length d of one side of each light emitting element 522 and the maximum value P of the interval between the light emitting elements 522 is set to P >d, more preferably P>2d, and even more preferably P>4d.
  • the relationship between the length d of one side of each light emitting element 522 and the maximum value P of the interval between the light emitting elements 522 is P ⁇ 5d. is preferred.
  • ⁇ represented by the above formula (1) is 1 or more, and is preferably 1.4 or more, for example, so that the light distribution ranges overlap sufficiently.
  • ⁇ 120 degrees
  • ⁇ (1/4) ⁇
  • d 0.35 mm
  • P is ⁇ 2 mm
  • L is 0.1 mm
  • n 1, and T is 0.7 mm.
  • ⁇ can be set to 1.4.
  • FIG. 8 is a diagram showing a configuration example of the illumination unit 102 according to this embodiment.
  • the optical system 400 includes a Koehler lens composed of lenses 402a, 402b, and 402c, a field stop 412, and an aperture stop 414, as in the comparative example. It can be lighting.
  • the light from the light source 500 according to this embodiment is uniform, it is not necessary to provide the diffusion plate 420 unlike the comparative example. Since each element of the optical system 400 is the same as that of the comparative example, the description thereof is omitted here.
  • the optical system 400 is not limited to Koehler illumination as described above, and may be critical illumination that does not include the field stop 412 .
  • the optical system 400 includes an aperture stop 414 provided between the light source 500 and the slide 300 , between the light source 500 and the aperture stop 414 , and between the aperture stop 414 and the slide 300 .
  • Critical illumination with multiple lenses 402 is not limited to Koehler illumination as described above, and may be critical illumination that does not include the field stop 412 .
  • the optical system 400 includes an aperture stop 414 provided between the light source 500 and the slide 300 , between the light source 500 and the aperture stop 414 , and between the aperture stop 414 and the slide 300 .
  • Critical illumination with multiple lenses 402 is critical illumination with multiple lenses 402 .
  • the optical system 400 has a configuration in which the light from the light source 500 is projected into the aperture of the aperture stop 414 .
  • a homogenizer (light homogenizing member) (not shown) is provided between the light source 500 and the aperture stop 414.
  • the homogenizer can be a diffusion plate 420, a rod integrator (not shown), or the like.
  • the light source 500 according to this embodiment having the configuration as described above, it is possible to uniform the luminance distribution on the light emitting surface (opening surface 510b).
  • FIG. 9 which is a diagram showing the simulation result of the luminance distribution on the light emitting surface of the light source 500 according to the embodiment of the present disclosure
  • the image of the light emitting element 522 cannot be recognized, in other words, the light emitting element 522
  • the luminance distribution becomes uniform without the occurrence of luminance peaks corresponding to the number of . That is, according to this embodiment, the luminance distribution of the light emitting surface (aperture surface 510b) has one peak and no inflection point.
  • the luminance distribution on the light emitting surface of the light source 500 becomes equivalent to that of the conventionally used lamp light source.
  • T is 0.7 mm
  • np is 1.8
  • ⁇ in the above formula (1) is 1.4.
  • FIG. 10 is a diagram showing a simulation result of luminance distribution on the light emitting surface of the light source 500 according to the embodiment of the present disclosure when ⁇ is 0.5. That is, when ⁇ is 0.5, luminance peaks are generated as many as the number of light emitting elements 522, and the luminance distribution is not uniform. 10, ⁇ is 120 degrees, ⁇ is (1/4) ⁇ , d is 0.35 mm, P is ⁇ 2 mm, L is 0.1 mm, and n is 1. , T is 0.7 mm, np is 1.8, and ⁇ in the above formula (1) is 0.5.
  • the luminance distribution on the light emitting surface of the light source 500 can be made uniform. Therefore, by using the light source 500 according to the present embodiment, the illumination unit 102 can ensure uniformity in the plane of the observation area and uniformity in the angular space.
  • the observation area can be irradiated with a high amount of light, there is no need to increase the gain of the imaging device (not shown) of the sensor unit 104, so the image captured by the sensor unit 104 noise can be suppressed.
  • the light from the light source 500 is uniform, it is not necessary to provide the diffusion plate 420, and as a result, an increase in the manufacturing cost of the optical system 400 can be suppressed.
  • the quality of the obtained image is high. In this case, it is possible to generate a wide-area image that does not give a sense of discomfort to the boundary of the image. Also, when machine learning is performed using the acquired images as training data, a highly accurate learning model can be obtained because the quality of the images used as training data is high. Furthermore, using such a learning model, highly accurate estimation, diagnosis, and the like can be performed.
  • the illumination unit (illumination device) 102 is not limited to being applied to the scanner 100 as described above. may be used as an illumination device for an optical microscope (not shown). Further, the scanner 100 is not limited to being used in the observation system 10 as described above, and may be used alone.
  • observation targets are not limited to biological samples.
  • the above-described embodiments of the present disclosure are not limited to application to medical or research applications, and industrial microscopes and the like that require high-precision analysis using images. is not particularly limited as long as it is used for
  • a microscope system 5000 shown in FIG. 11 includes a microscope device 5100 , a control section 5110 and an information processing section 5120 .
  • the microscope device 5100 has a light irradiation section 5101 , an optical section 5102 and a signal acquisition section 5103 .
  • the microscope device 5100 may further have a sample placement section 5104 on which the biological sample S is placed.
  • the configuration of the microscope apparatus is not limited to that shown in FIG. It may be used as the light irradiation unit 5101 .
  • the light irradiation section 5101 may be arranged such that the sample mounting section 5104 is sandwiched between the light irradiation section 5101 and the optical section 5102, and may be arranged on the side where the optical section 5102 exists, for example.
  • the microscope apparatus 5100 may be configured to be able to perform one or more of bright field observation, phase contrast observation, differential interference contrast observation, polarization observation, fluorescence observation, and dark field observation.
  • the microscope system 5000 may be configured as a so-called WSI (Whole Slide Imaging) system or a digital pathology imaging system, and can be used for pathological diagnosis.
  • Microscope system 5000 may also be configured as a fluorescence imaging system, in particular a multiplex fluorescence imaging system.
  • the microscope system 5000 may be used to perform intraoperative pathological diagnosis or remote pathological diagnosis.
  • the microscope device 5100 acquires data of the biological sample S obtained from the subject of the surgery, and transmits the data to the information processing unit 5120. and can be sent.
  • the microscope device 5100 can transmit the acquired data of the biological sample S to the information processing unit 5120 located in a place (another room, building, etc.) away from the microscope device 5100. .
  • the information processing section 5120 receives and outputs the data. Further, the user of the information processing section 5120 can make a pathological diagnosis based on the output data.
  • the biological sample S may be a sample containing a biological component.
  • the biological components may be tissues, cells, liquid components of a living body (blood, urine, etc.), cultures, or living cells (cardiomyocytes, nerve cells, fertilized eggs, etc.).
  • the biological sample may be a solid substance, a specimen fixed with a fixing reagent such as paraffin, or a solid substance formed by freezing.
  • the biological sample can be a section of the solid.
  • a specific example of the biological sample is a section of a biopsy sample.
  • the above biological sample may be one that has undergone processing such as staining or labeling.
  • the treatment may be staining for indicating the morphology of biological components or for indicating substances (surface antigens, etc.) possessed by biological components, such as HE (Hematoxylin-Eosin) staining, immunohistochemistry staining, and the like. can be mentioned.
  • the biological sample may have been subjected to the above treatment with one or more reagents, and the reagents may be fluorescent dyes, coloring reagents, fluorescent proteins, or fluorescently labeled antibodies.
  • the specimen may be one prepared from a tissue sample for the purpose of pathological diagnosis or clinical examination.
  • the specimen is not limited to the human body, and may be derived from animals, plants, or other materials.
  • the type of specimen used e.g., organs or cells, etc.
  • the type of target disease e.g., the type of target disease
  • the subject's attributes e.g., age, sex, blood type, race, etc.
  • the subject's lifestyle For example, eating habits, exercise habits, smoking habits, etc.
  • the specimens may be managed with identification information (one-dimensional or two-dimensional code such as bar code or QR code (registered trademark)) that allows each specimen to be identified.
  • the light irradiation unit 5101 is a light source for illuminating the biological sample S and an optical system for guiding the light irradiated from the light source to the specimen.
  • the light source may irradiate the biological sample with visible light, ultraviolet light, or infrared light, or a combination thereof.
  • the light source may be one or more of a halogen light source, a laser light source, an LED light source, a mercury light source, and a xenon light source.
  • a plurality of light source types and/or wavelengths may be used in fluorescence observation, and may be appropriately selected by those skilled in the art.
  • the light irradiation unit 5101 can have a transmissive, reflective, or episcopic (coaxial or lateral) configuration.
  • the optical section 5102 is configured to guide the light from the biological sample S to the signal acquisition section 5103 .
  • the optical unit 5102 can be configured to allow the microscope device 5100 to observe or image the biological sample S.
  • Optics 5102 may include an objective lens. The type of objective lens may be appropriately selected by a person skilled in the art according to the observation method.
  • the optical unit 5102 may include a relay lens for relaying the image magnified by the objective lens to the signal acquisition unit.
  • the optical section 5102 may further include optical components other than the objective lens and relay lens, eyepiece lens, phase plate, condenser lens, and the like.
  • the optical section 5102 may further include a wavelength separation section configured to separate light having a predetermined wavelength from the light from the biological sample S.
  • the wavelength separation section may be configured to selectively allow light of a predetermined wavelength or range of wavelengths to reach the signal acquisition section.
  • the wavelength separator may include, for example, one or more of a filter that selectively transmits light, a polarizing plate, a prism (Wollaston prism), and a diffraction grating.
  • the optical components included in the wavelength separation section may be arranged, for example, on the optical path from the objective lens to the signal acquisition section.
  • the wavelength separation unit is provided in the microscope device when fluorescence observation is performed, particularly when an excitation light irradiation unit is included.
  • the wavelength separator may be configured to separate fluorescent light from each other or white light and fluorescent light.
  • the signal acquisition unit 5103 can be configured to receive light from the biological sample S and convert the light into an electrical signal, particularly a digital electrical signal.
  • the signal acquisition unit 5103 may be configured to acquire data regarding the biological sample S based on the electrical signal.
  • the signal acquisition unit 5103 may be configured to acquire data of an image (image, particularly a still image, a time-lapse image, or a moving image) of the biological sample S. can be configured to acquire data for an image obtained by
  • the signal acquisition unit 5103 includes one or more image sensors having a plurality of pixels arranged one-dimensionally or two-dimensionally, a CMOS (Complementary Metal Oxide Semiconductor), a CCD (Charge Coupled Device), or the like.
  • CMOS Complementary Metal Oxide Semiconductor
  • CCD Charge Coupled Device
  • the signal acquisition unit 5103 may include an image sensor for acquiring a low-resolution image and an image sensor for acquiring a high-resolution image, or an image sensor for sensing for AF (Auto Focus) and the like and an image sensor for observation.
  • An imaging device for image output may also be included.
  • the image sensor includes a signal processing unit (CPU (Central Processing Unit) that performs signal processing using pixel signals from each pixel, a DSP (Digital Signal Processor), and one or two memories. above), and an output control unit that controls output of image data generated from the pixel signals and processed data generated by the signal processing unit.
  • the imaging device including the plurality of pixels, the signal processing section, and the output control section can preferably be configured as a one-chip semiconductor device.
  • the microscope system 5000 may further include an event detection sensor.
  • the event detection sensor includes a pixel that photoelectrically converts incident light, and can be configured to detect, as an event, a change in luminance of the pixel exceeding a predetermined threshold.
  • the event detection sensor may be asynchronous.
  • the control unit 5110 controls imaging by the microscope device 5100 .
  • the control unit 5110 can drive the movement of the optical unit 5102 and/or the sample placement unit 5104 to adjust the positional relationship between the optical unit 5102 and the sample placement unit 5104.
  • the control unit 5110 can move the optical unit 5102 and/or the sample mounting unit 5104 in a direction toward or away from each other (for example, the optical axis direction of the objective lens).
  • the control section 5110 may move the optical section 5102 and/or the sample placement section 5104 in any direction on a plane perpendicular to the optical axis direction.
  • the control unit 5110 may control the light irradiation unit 5101 and/or the signal acquisition unit 5103 for imaging control.
  • the sample mounting section 5104 may be configured such that the position of the biological sample S on the sample mounting section 5104 can be fixed, and may be a so-called stage.
  • the sample placement section 5104 can be configured to move the position of the biological sample S in the optical axis direction of the objective lens and/or in a direction perpendicular to the optical axis direction.
  • the information processing section 5120 can acquire data (such as imaging data) acquired by the microscope device 5100 from the microscope device 5100 .
  • the information processing section 5120 can perform image processing on captured data.
  • the image processing may include an unmixing process, in particular a spectral unmixing process.
  • the unmixing process is a process of extracting data of light components of a predetermined wavelength or wavelength range from the imaging data to generate image data, or removing data of light components of a predetermined wavelength or wavelength range from the imaging data. It can include processing and the like.
  • the image processing may include an autofluorescence separation process for separating the autofluorescence component and the dye component of the tissue section, and a fluorescence separation process for separating the wavelengths between dyes having different fluorescence wavelengths.
  • autofluorescence separation processing a process of removing an autofluorescence component from the image information of the other specimen using an autofluorescence signal extracted from one of a plurality of specimens having the same or similar properties may be performed.
  • the information processing section 5120 may transmit data for imaging control by the control section 5110, and the control section 5110 receiving the data may control imaging by the microscope apparatus 5100 according to the data.
  • the information processing section 5120 may be configured as an information processing device such as a general-purpose computer, and may have a CPU, RAM (Random Access Memory), and ROM (Read Only Memory).
  • the information processing section 5120 may be included in the housing of the microscope device 5100 or may be outside the housing.
  • Various processing or functions by the information processing section 5120 may be realized by a server computer or cloud connected via a network.
  • a method of imaging the biological sample S by the microscope device 5100 may be appropriately selected by a person skilled in the art according to the type of the biological sample S, the purpose of imaging, and the like. An example of the imaging method will be described below with reference to FIGS. 12 and 13.
  • FIG. 12 and 13 are diagrams showing examples of imaging methods.
  • the microscope device 5100 can first identify an imaging target region.
  • the imaging target region may be specified so as to cover the entire region in which the biological sample S exists, or a target portion of the biological sample S (a target tissue section, a target cell, or a target lesion where the target lesion exists). may be specified to cover the Next, the microscope device 5100 divides the imaging target region into a plurality of divided regions of a predetermined size, and the microscope device 5100 sequentially images each divided region. As a result, an image of each divided area is obtained.
  • the microscope device 5100 identifies an imaging target region R that covers the entire biological sample S. Then, the microscope device 5100 divides the imaging target region R into 16 divided regions. Then, the microscope device 5100 can image the divided region R1, and then any region included in the imaging target region R, such as a region adjacent to the divided region R1. Furthermore, the microscope device 5100 captures images of the divided areas until there are no unimaged divided areas. Note that the microscope device 5100 may also capture an area other than the imaging target area R based on the captured image information of the divided area. At this time, the positional relationship between the microscope device 5100 and the sample mounting section 5104 is adjusted in order to image the next divided area after imaging a certain divided area. The adjustment can be performed by moving the microscope device 5100, moving the sample placement section 5104, or moving both of them.
  • the imaging device that captures each divided area may be a two-dimensional imaging device (area sensor) or a one-dimensional imaging device (line sensor).
  • the signal acquisition unit 5103 may image each divided area via the optical unit 5102 .
  • the imaging of each divided region may be performed continuously while moving the microscope device 5100 and/or the sample placement unit 5104, or when imaging each divided region, the microscope device 5100 and/or Alternatively, the movement of the sample placement section 5104 may be stopped.
  • the imaging target region may be divided so that the divided regions partially overlap each other, or the imaging target region may be divided so that the divided regions do not overlap.
  • Each divided area may be imaged multiple times by changing imaging conditions such as focal length and/or exposure time.
  • the information processing section 5120 can stitch a plurality of adjacent divided regions to generate image data of a wider region. By performing the stitching process over the entire imaging target area, it is possible to obtain an image of a wider area of the imaging target area. Further, image data with lower resolution can be generated from the image of the divided area or the image subjected to the stitching process.
  • the microscope device 5100 can first identify an imaging target region.
  • the imaging target region may be specified so as to cover the entire region where the biological sample S is present, or a target portion (a target tissue section or a portion where target cells are present) of the biological sample S. may be specified to cover.
  • the microscope device 5100 scans a partial region (also referred to as a “divided scan region”) of the imaging target region in one direction (also referred to as a “scanning direction”) within a plane perpendicular to the optical axis. Take an image.
  • the microscope device 5100 scans the divided scan area next to the scan area. Then, the microscope device 5100 repeats these scanning operations until the entire imaging target region is imaged.
  • the microscope device 5100 identifies the region (gray portion) where the tissue section exists in the biological sample S as the imaging target region Sa. Then, the microscope device 5100 scans the divided scan area Rs in the imaging target area Sa in the Y-axis direction. After completing scanning of the divided scan region Rs, the microscope device 5100 next scans an adjacent divided scan region in the X-axis direction. The microscope device 5100 repeats this operation until scanning is completed for the entire imaging target area Sa.
  • the positional relationship between the microscope device 5100 and the sample placement section 5104 is adjusted for scanning each divided scan area and for imaging the next divided scan area after imaging a certain divided scan area.
  • the adjustment may be performed by moving the microscope device 5100, moving the sample placement section 5104, or moving both of them.
  • the imaging device that captures each divided scan area may be a one-dimensional imaging device (line sensor) or a two-dimensional imaging device (area sensor).
  • the signal acquisition unit 5103 may capture an image of each divided area via an enlarging optical system.
  • the imaging of each divided scan region may be performed continuously while moving the microscope device 5100 and/or the sample placement unit 5104 .
  • the imaging target area may be divided such that the divided scan areas partially overlap each other, or the imaging target area may be divided so that the divided scan areas do not overlap.
  • Each divided scan area may be imaged multiple times while changing imaging conditions such as focal length and/or exposure time.
  • the information processing section 5120 can stitch a plurality of adjacent divided scan regions to generate image data of a wider region. By performing the stitching process over the entire imaging target area, it is possible to obtain an image of a wider area of the imaging target area. Further, image data with lower resolution can be generated from images of divided scan regions or images subjected to stitching processing.
  • a diagnosis support system in which a doctor or the like observes cells and tissues collected from a patient and diagnoses a lesion.
  • This diagnosis support system may be a WSI (Whole Slide Imaging) system that diagnoses or supports diagnosis of lesions based on images acquired using digital pathology technology.
  • FIG. 14 is a diagram showing an example of a schematic configuration of a diagnostic support system 5500 to which the technology according to the present disclosure is applied.
  • the diagnostic support system 5500 includes one or more pathology systems 5510.
  • a medical information system 5530 and a derivation device 5540 may also be included.
  • Each of the one or more pathology systems 5510 is a system mainly used by pathologists, and is installed in laboratories and hospitals, for example.
  • Each pathology system 5510 may be installed in a different hospital, and each uses various networks such as WAN (Wide Area Network) (including the Internet), LAN (Local Area Network), public line network, and mobile communication network. It is connected to the medical information system 5530 and the derivation device 5540 via.
  • WAN Wide Area Network
  • LAN Local Area Network
  • public line network public line network
  • mobile communication network mobile communication network
  • Each pathology system 5510 includes a microscope (specifically, a microscope used in combination with digital imaging technology) 5511, a server 5512, a display control device 5513, and a display device 5514.
  • a microscope specifically, a microscope used in combination with digital imaging technology
  • server 5512 a server 5512
  • display control device 5513 a display device 5514.
  • the microscope 5511 has the function of an optical microscope, photographs an observation object contained in a glass slide, and acquires a pathological image, which is a digital image.
  • Observation objects are, for example, tissues and cells collected from a patient, and may be pieces of flesh of organs, saliva, blood, and the like.
  • microscope 5511 functions as scanner 30 shown in FIG.
  • the server 5512 stores and saves pathological images acquired by the microscope 5511 in a storage unit (not shown). Further, when receiving a viewing request from the display control device 5513 , the server 5512 searches for pathological images from a storage unit (not shown) and sends the searched pathological images to the display control device 5513 .
  • the display control device 5513 sends to the server 5512 the pathological image viewing request received from the user. Then, the display control device 5513 displays the pathological image received from the server 5512 on the display device 5514 using liquid crystal, EL (Electro-Luminescence), CRT (Cathode Ray Tube), or the like. Note that the display device 5514 may be compatible with 4K or 8K, and is not limited to one device, and may be a plurality of devices.
  • the observation target is a solid object such as a piece of flesh of an organ
  • the observation target may be, for example, a stained slice.
  • a sliced piece may be produced, for example, by slicing a block piece excised from a specimen such as an organ. Also, when slicing, the block pieces may be fixed with paraffin or the like.
  • staining thin sections including general staining that indicates the morphology of tissues such as HE (Hematoxylin-Eosin) staining, immunostaining that indicates the immune status of tissues such as IHC (Immunohistochemistry) staining, and fluorescent immunostaining.
  • general staining that indicates the morphology of tissues
  • immunostaining that indicates the immune status of tissues
  • IHC Immunohistochemistry
  • fluorescent immunostaining may be applied.
  • one thin section may be stained with a plurality of different reagents, or two or more thin sections (also referred to as adjacent thin sections) continuously cut out from the same block piece may be stained with different reagents. may be dyed using
  • the microscope 5511 can include a low-resolution imaging unit for low-resolution imaging and a high-resolution imaging unit for high-resolution imaging.
  • the low-resolution imaging section and the high-resolution imaging section may be different optical systems, or may be the same optical system. In the case of the same optical system, the resolution of the microscope 5511 may be changed according to the imaging target.
  • the glass slide containing the observation target is placed on the stage located within the angle of view of the microscope 5511.
  • the microscope 5511 first acquires the entire image within the angle of view using the low-resolution imaging unit, and specifies the region of the observation object from the acquired entire image. Subsequently, the microscope 5511 divides the region where the observation target exists into a plurality of divided regions of a predetermined size, and sequentially captures each divided region by the high-resolution imaging unit, thereby obtaining a high-resolution image of each divided region. do.
  • the stage may be moved, the imaging optical system may be moved, or both of them may be moved.
  • each divided area may overlap adjacent divided areas in order to prevent occurrence of an imaging omission area due to unintended slippage of the glass slide.
  • the whole image may contain identification information for associating the whole image with the patient. This identification information may be, for example, a character string, a QR code (registered trademark), or the like.
  • a high-resolution image acquired by the microscope 5511 is input to the server 5512.
  • the server 5512 divides each high resolution image into smaller size partial images (hereinafter referred to as tile images). For example, the server 5512 divides one high-resolution image into a total of 100 tile images of 10 ⁇ 10. At that time, if adjacent divided areas overlap, the server 5512 may perform stitching processing on adjacent high-resolution images using a technique such as template matching. In that case, the server 5512 may generate tile images by dividing the entire high-resolution image stitched together by the stitching process. However, the generation of tile images from high-resolution images may be performed before the above stitching process.
  • the server 5512 can generate tile images of smaller sizes by further dividing the tile images. Such generation of tile images may be repeated until a tile image having the size set as the minimum unit is generated.
  • the server 5512 After generating tile images of the minimum unit in this way, the server 5512 performs tile composition processing for generating a single tile image by compositing a predetermined number of adjacent tile images for all tile images. This tile synthesis process can be repeated until finally one tile image is generated.
  • a pyramid-structured tile image group in which each layer is composed of one or more tile images is generated.
  • a tile image in one layer and a tile image in a different layer have the same number of pixels, but different resolutions. For example, when synthesizing a total of four 2 ⁇ 2 tile images to generate one upper layer tile image, the resolution of the upper layer tile image is half the resolution of the lower layer tile image used for synthesis. It has become.
  • the generated pyramid-structured tile image group is stored in a storage unit (not shown) together with, for example, identification information (referred to as tile identification information) that can uniquely identify each tile image.
  • identification information referred to as tile identification information
  • the server 5512 receives a tile image acquisition request including tile identification information from another device (for example, the display control device 5513 or the derivation device 5540), the server 5512 transmits the tile image corresponding to the tile identification information to the other device. do.
  • tile images which are pathological images
  • a specific pathological image and other pathological images corresponding to imaging conditions different from the specific imaging condition and having the same region as the specific pathological image are generated. They may be displayed side by side.
  • Specific shooting conditions may be specified by the viewer.
  • pathological images of the same region corresponding to each imaging condition may be displayed side by side.
  • the server 5512 may store the pyramid-structured tile image group in a storage device other than the server 5512, such as a cloud server. Furthermore, part or all of the tile image generation processing as described above may be executed by a cloud server or the like.
  • the display control device 5513 extracts a desired tile image from the pyramid-structured tile image group according to the user's input operation, and outputs it to the display device 5514 . Through such processing, the user can obtain the feeling of observing the observation object while changing the observation magnification. That is, the display control device 5513 functions as a virtual microscope. The virtual observation magnification here actually corresponds to the resolution.
  • a high-resolution image may be obtained by photographing the divided areas while the stage is repeatedly stopped and moved, or a high-resolution image on the strip may be obtained by photographing the divided areas while moving the stage at a predetermined speed. good too.
  • the process of generating tile images from high-resolution images is not an essential configuration, and by changing the resolution of the entire high-resolution image stitched together by the stitching process, images with gradual changes in resolution can be created. may be generated. Even in this case, it is possible to present the user with a step-by-step process from a low-resolution image of a wide area to a high-resolution image of a narrow area.
  • the medical information system 5530 is a so-called electronic medical record system, and stores information related to diagnosis, such as patient identification information, patient disease information, test information and image information used for diagnosis, diagnosis results, and prescription drugs.
  • information related to diagnosis such as patient identification information, patient disease information, test information and image information used for diagnosis, diagnosis results, and prescription drugs.
  • a pathological image obtained by photographing an observation target of a certain patient can be temporarily stored via the server 5512 and then displayed on the display device 5514 by the display control device 5513 .
  • a pathologist using the pathological system 5510 makes a pathological diagnosis based on the pathological image displayed on the display device 5514 .
  • Pathological diagnosis results made by the pathologist are stored in the medical information system 5530 .
  • a derivation device 5540 may perform analysis on pathological images.
  • a learning model created by machine learning can be used for this analysis.
  • the derivation device 5540 may derive a classification result of a specific region, a tissue identification result, or the like as the analysis result. Further, the deriving device 5540 may derive identification results such as cell information, number, position, brightness information, and scoring information for them. These pieces of information derived by the derivation device 5540 may be displayed on the display device 5514 of the pathology system 5510 as diagnosis support information.
  • the derivation device 5540 may be a server system configured with one or more servers (including cloud servers). Also, the derivation device 5540 may be configured to be incorporated in, for example, the display control device 5513 or the server 5512 in the pathological system 5510 . That is, various analyzes on pathological images may be performed within the pathological system 5510 .
  • the technology according to the present disclosure can be preferably applied to the microscope 5511 as described above among the configurations described above.
  • the technology according to the present disclosure to the microscope 5511, it is possible to obtain a clearer pathological image, and thus it is possible to more accurately diagnose a lesion.
  • the configuration described above can be applied not only to the diagnostic support system, but also to general biological microscopes such as confocal microscopes, fluorescence microscopes, and video microscopes that use digital imaging technology.
  • the object to be observed may be a biological sample such as cultured cells, fertilized eggs, or sperm, a biological material such as a cell sheet or a three-dimensional cell tissue, or a living body such as a zebrafish or mouse.
  • the object to be observed is not limited to the glass slide, and can be observed while being stored in a well plate, petri dish, or the like.
  • a moving image may be generated from still images of the observed object acquired using a microscope that utilizes digital imaging technology.
  • a moving image may be generated from still images captured continuously over a predetermined period of time, or an image sequence may be generated from still images captured at predetermined intervals.
  • it is possible to observe the movements of cancer cells, nerve cells, myocardial tissue, sperm, etc. such as pulsation, elongation, and migration, and the division process of cultured cells and fertilized eggs. It becomes possible to analyze the dynamic features of objects using machine learning.
  • each component of each illustrated device is functionally conceptual, and does not necessarily need to be physically configured as illustrated.
  • the specific form of distribution and integration of each device is not limited to the one shown in the figure, and all or part of them can be functionally or physically distributed and integrated in arbitrary units according to various loads and usage conditions. Can be integrated and configured.
  • the present technology can also take the following configuration.
  • a light source having a housing, a plurality of light emitting elements mounted on the bottom surface of the housing, and a phosphor layer provided above the plurality of light emitting elements; an optical system that collects light from the light source; with The FWHM angle of each light emitting element is ⁇ , the length of one side of the light emitting element is d, the maximum distance between the light emitting elements adjacent to each other is P, and the distance between the light emitting element and the phosphor layer is When L is the distance between the , provided to satisfy the following formula (1), Illumination device for observation equipment.
  • the plurality of light emitting elements are provided so as to satisfy the following formula (2), The illumination device for an observation device according to (1) above.
  • the plurality of light emitting elements are provided so as to satisfy the following formula (3), The illumination device for an observation device according to (2) above.
  • the optical system is a field stop provided between the illumination device and the sample; an aperture stop provided between the field stop and the sample; a plurality of lenses provided between the illumination device and the field stop, between the field stop and the aperture stop, and between the aperture stop and the sample;
  • the optical system is an aperture stop provided between the illumination device and the sample; a plurality of lenses provided between the illumination device and the aperture stop and between the aperture stop and the sample;
  • the optical system is further comprising a light homogenizing member provided between the illumination device and the aperture stop;
  • the phosphor layer contains at least one or more phosphors.
  • the phosphor layer includes a plurality of types of phosphors that emit light in different wavelength bands.
  • the light source irradiates the biological sample with light.
  • a light source having a housing, a plurality of light emitting elements mounted on the bottom surface of the housing, and a phosphor layer provided above the plurality of light emitting elements,
  • the FWHM angle of each light emitting element is ⁇
  • the length of one side of the light emitting element is d
  • the maximum distance between the light emitting elements adjacent to each other is P
  • the distance between the light emitting element and the phosphor layer is
  • L is the distance between the , provided to satisfy the following formula (1), Illumination device for observation equipment.
  • a light source having a housing, a plurality of light emitting elements mounted on the bottom surface of the housing, and a phosphor layer provided above the plurality of light emitting elements; an optical system that collects light from the light source;
  • the housing has an opening face provided to face the bottom face and through which light from the plurality of light emitting elements is emitted to the outside, The plurality of light emitting elements are provided on the bottom surface so that the brightness distribution of the aperture surface has one peak and no inflection point exists. Illumination device for observation equipment.
  • a light source having a housing, a plurality of light emitting elements mounted on the bottom surface of the housing, and a phosphor layer provided above the plurality of light emitting elements; an optical system that collects light from the light source;
  • the housing has an opening face provided to face the bottom face and through which light from the plurality of light emitting elements is emitted to the outside,
  • the plurality of light emitting elements are provided on the bottom surface such that a part of the light distribution range of each of the light emitting elements overlaps with each other on the opening surface. Illumination device for observation equipment.
  • an illumination device that irradiates light, an objective lens that magnifies the sample, and with The lighting device a light source having a housing, a plurality of light emitting elements mounted on the bottom surface of the housing, and a phosphor layer provided above the plurality of light emitting elements; an optical system that collects light from the light source; has The FWHM angle of each light emitting element is ⁇ , the length of one side of the light emitting element is d, the maximum distance between the light emitting elements adjacent to each other is P, and the distance between the light emitting element and the phosphor layer is When L is the distance between the , provided to satisfy the following formula (1), Observation device. (17) The observation device according to (16) above, further comprising an eyepiece.
  • the observation device further comprising an imaging unit made up of an imaging element.
  • the observation device has an illumination device that emits light and an imaging unit that includes an imaging element that images the biological sample,
  • the lighting device a light source having a housing, a plurality of light emitting elements mounted on the bottom surface of the housing, and a phosphor layer provided above the plurality of light emitting elements; an optical system that collects light from the light source; with The FWHM angle of each light emitting element is ⁇ , the length of one side of the light emitting element is d, the maximum distance between the light emitting elements adjacent to each other is P, and the distance between the light emitting element and the phosphor layer is When L is the distance between the , provided to satisfy the following formula (1), observation system.

Abstract

L'invention concerne un dispositif d'éclairage (102) pour un dispositif d'observation, le dispositif d'éclairage comprenant : une source de lumière (500) comportant un boîtier (510), une pluralité d'éléments électroluminescents (522) montés sur une surface inférieure du boîtier, et une couche de phosphore (524) disposée au-dessus de la pluralité d'éléments électroluminescents ; et un système optique (400) pour collecter la lumière provenant de la source de lumière. Lorsque l'angle de FWHM de chacun des éléments électroluminescents est désigné par θ, la longueur d'un côté de l'élément électroluminescent est désignée par d, la valeur maximale d'espacement entre les éléments électroluminescents adjacents les uns aux autres est désignée par P, la distance entre l'élément électroluminescent et la couche de phosphore est désignée par L, l'indice de réfraction d'un milieu dans le boîtier est désigné par n, l'épaisseur de la couche de phosphore est désignée par T, et l'indice de réfraction de la couche de phosphore est désigné par np, la pluralité d'éléments électroluminescents sont disposés de façon à satisfaire l'expression (1).
PCT/JP2022/005575 2021-03-31 2022-02-14 Dispositif d'éclairage pour dispositif d'observation, dispositif d'observation et système d'observation WO2022209349A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2021060432A JP2022156634A (ja) 2021-03-31 2021-03-31 観察装置用照明装置、観察装置及び観察システム
JP2021-060432 2021-03-31

Publications (1)

Publication Number Publication Date
WO2022209349A1 true WO2022209349A1 (fr) 2022-10-06

Family

ID=83455861

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2022/005575 WO2022209349A1 (fr) 2021-03-31 2022-02-14 Dispositif d'éclairage pour dispositif d'observation, dispositif d'observation et système d'observation

Country Status (2)

Country Link
JP (1) JP2022156634A (fr)
WO (1) WO2022209349A1 (fr)

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006337925A (ja) * 2005-06-06 2006-12-14 Olympus Corp 顕微鏡の照明装置
JP2018200332A (ja) * 2017-05-25 2018-12-20 オリンパス株式会社 顕微鏡用照明装置、及び、顕微鏡
JP2019531513A (ja) * 2016-09-30 2019-10-31 深▲せん▼市玲涛光電科技有限公司Ｓｈｅｎｚｈｅｎ Ｌｔ Ｏｐｔｏｅｌｅｃｔｒｏｎｉｃｓ Ｃｏ．，Ｌｔｄ． 光源モジュール、表示装置および光源モジュールの製造方法

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006337925A (ja) * 2005-06-06 2006-12-14 Olympus Corp 顕微鏡の照明装置
JP2019531513A (ja) * 2016-09-30 2019-10-31 深▲せん▼市玲涛光電科技有限公司Ｓｈｅｎｚｈｅｎ Ｌｔ Ｏｐｔｏｅｌｅｃｔｒｏｎｉｃｓ Ｃｏ．，Ｌｔｄ． 光源モジュール、表示装置および光源モジュールの製造方法
JP2018200332A (ja) * 2017-05-25 2018-12-20 オリンパス株式会社 顕微鏡用照明装置、及び、顕微鏡

Also Published As

Publication number Publication date
JP2022156634A (ja) 2022-10-14

Similar Documents

Publication Publication Date Title
KR101349664B1 (ko) 발광소자 조명 소스를 지닌 현미경
AU2014265382B2 (en) Microscopy of a tissue sample using structured illumination
CN105103190B (zh) 全视野载玻片多光谱成像系统和方法
CN105308949B (zh) 图像获取装置、图像获取方法以及记录介质
WO2010109811A1 (fr) Dispositif d'observation
JPS59160743A (ja) 螢光によつて検出可能な現象の観察および定量化装置
JP2021193459A (ja) 二重光学経路および単一撮像センサを使用した低解像度スライド撮像、スライドラベル撮像および高解像度スライド撮像
JP2014098575A (ja) 画像取得装置および画像取得方法
JP2013044967A (ja) 顕微鏡システム、標本画像生成方法及びプログラム
US10342433B2 (en) Insitu diagnostic tool for digital pathology
CN103168265A (zh) 成像系统和其关联的方法
WO2022209349A1 (fr) Dispositif d'éclairage pour dispositif d'observation, dispositif d'observation et système d'observation
WO2022209262A1 (fr) Dispositif d'éclairage pour dispositif d'observation d'échantillon biologique, dispositif d'observation d'échantillon biologique, dispositif d'éclairage pour dispositif d'observation et système d'observation
WO2022050109A1 (fr) Dispositif de traitement d'images, procédé de traitement d'images, et système de traitement d'images
WO2022270015A1 (fr) Dispositif d'observation d'échantillon biologique et système d'observation d'échantillon biologique
WO2022202233A1 (fr) Dispositif de traitement d'informations, procédé de traitement d'informations, système de traitement d'informations et modèle de conversion
WO2022259647A1 (fr) Dispositif de traitement d'informations, procédé de traitement d'informations et système de microscope
US11335454B2 (en) Biopsy device for digital pathology and artificial intelligent analytics
WO2023248954A1 (fr) Système d'observation d'échantillon biologique, procédé d'observation d'échantillon biologique et procédé de création d'ensemble de données
WO2022138254A1 (fr) Casier de stockage de lames de verre, dispositif de stockage de lames et système d'imagerie de lames en verre
WO2023157755A1 (fr) Dispositif de traitement d'informations, système d'analyse d'échantillon biologique et procédé d'analyse d'échantillon biologique
US20230085045A1 (en) Microscope for high-resolution and specific analysis of biological substances, and method of analysis
WO2023157756A1 (fr) Dispositif de traitement d'informations, système d'analyse d'échantillon biologique et procédé d'analyse d'échantillon biologique
WO2021220857A1 (fr) Dispositif de traitement d'image, procédé de traitement d'image et système de traitement d'image
WO2021157397A1 (fr) Appareil et système de traitement d'information

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 22779577

Country of ref document: EP

Kind code of ref document: A1

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 22779577

Country of ref document: EP

Kind code of ref document: A1