• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
  • 引用文献
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    • 专利摘要:
    The invention is a method for identifying the state of a cell contained in a sample having the illumination of the sample using a light source, the latter producing an incident light wave propagating towards the sample, then acquiring, with the aid of a matrix photodetector, an image of the sample, the sample being disposed between said light source and the photodetector, so that the matrix photodetector is exposed to a light wave comprising interference between the incident light wave and a diffraction wave produced by each particle. The method is characterized in that it comprises the application of a digital reconstruction algorithm to the image acquired by the photodetector, for estimating a characteristic quantity of the light wave reaching the detector, at a plurality of distances from the photodetector . The value of the characteristic quantity, or its evolution as a function of the distance makes it possible to identify the particle.
    公开号:FR3034197A1
    申请号:FR1552445
    申请日:2015-03-24
    公开日:2016-09-30
    发明作者:Cedric Allier；Geoffrey Esteban
    申请人:Iprasense Sas；Commissariat a lEnergie Atomique CEA；Commissariat a lEnergie Atomique et aux Energies Alternatives CEA；
    IPC主号:
    专利说明:

    [0001] BACKGROUND OF THE INVENTION The invention is in the field of cell analysis, and more specifically in the control of cell proliferation, in incubators or biological reactors. PRIOR ART Controlling the development of cells in incubators or in biological reactors is an essential step in the production process of cells. In these applications, the cells are placed in a culture medium, conducive to their development. Their number and condition are regularly checked, especially if they are alive or dead. These control operations require the use of a microscope, the cells being previously labeled with a fluorescent label or a chromophore, the level of fluorescence of cells depending on whether they are alive or dead. Such a method has certain disadvantages: firstly, it requires the use of a microscope, expensive and bulky equipment. In addition, since the field of view is small, the analysis of a spatially extended sample requires time because the sample must be moved in front of the microscope. Moreover, labeling with a fluorescent label or chromophore can have consequences on cell development. A search method for cells is therefore sought, and in particular a means for discriminating living or dead cells, which is simple, inexpensive, without marking and offers a wide field of observation. SUMMARY OF THE INVENTION The invention responds to this problem by providing a method for determining the state of a cell, said cell being placed in a sample, the method comprising the steps of: illuminating said sample with the aid of a light source, the light source producing an incident light wave propagating towards the sample along an axis of propagation, by acquisition, using a matrix photodetector, of an image of the sample, sample being disposed between said light source and said matrix photodetector, such that the matrix photodetector is exposed to a light wave comprising interference between the incident light wave and a diffraction wave produced by each cell - determination of a position of said cell in a plane parallel to a detection plane according to which the matrix photodetector extends, application of a recognition algorithm digital construction to said acquired image, so as to determine at least one characteristic quantity of said light wave to which the matrix photodetector is exposed, at a distance from said matrix photodetector, said reconstruction distance, according to said axis of propagation, classification of said cell as a function of the value of said characteristic quantity, at said position, and at said reconstruction distance, the classification making it possible to determine the state of said cell among predetermined states.
    [0002] In particular, the predetermined states may comprise a living state and a dead state. The method is then able to classify an examined cell and determine if it is dead or alive. The characteristic quantity is obtained in particular by estimating, at said reconstruction distance, a complex expression of the light wave to which the matrix photodetector is exposed. The characteristic quantity can be obtained from the module or argument of said complex expression. According to one embodiment, said characteristic quantity is determined at a plurality of reconstruction distances along said propagation axis, the classification being then performed as a function of the evolution of said characteristic quantity along said propagation axis. For example, the classification is performed by comparing said evolution of said characteristic quantity with predetermined standard profiles. The method may comprise a step of reconstructing an image of said characteristic quantity in a plane parallel to the detection plane, and at said reconstruction distance, the value of said characteristic quantity at said position of the cell, and at said distance of reconstruction, being determined according to this image.
    [0003] The position of each cell, in a plane parallel to the detection plane, can be determined using the image acquired by the matrix photodetector or with the aid of a reconstructed image described in the previous paragraph. The light source can be a spatially coherent source. It may in particular be a light emitting diode. The light source can also be temporally coherent; it can in particular be a laser diode. The matrix photodetector comprises a matrix of pixels capable of collecting the light wave to which the photodetector is exposed. The distance between the pixels and the sample may vary between 50 μm and 2 cm, and preferably between 100 μm and 5 mm. Preferably the sample is not disposed in direct contact with the pixels of the matrix photodetector. Preferably, no magnification optics are disposed between the sample and the matrix photodetector. An object of the invention is also a device for discriminating a living cell from a dead cell, said cell being arranged in a sample, the device comprising: a light source arranged to produce an incident light wave along an axis of propagating, in the direction of said sample, a matrix photodetector, arranged to acquire an image of the sample, while being exposed to a light wave, resulting from the interference between said incident light wave and a diffraction wave formed by said cell, a support, for holding the sample between said light source and the matrix photodetector, the device being characterized in that it comprises a processor configured to implement the following steps: - determining a position of said cell in a plane parallel to a detection plane, according to which the matrix photodetector extends, application of an algorithm for digital reconstruction to said acquired image, so as to determine at least one characteristic quantity of the light wave to which the matrix photodetector is exposed, at a distance from the latter, said reconstruction distance, along the axis of propagation, 3034197 4 classification of said cell as a function of the value of said characteristic quantity, at said position and at said reconstruction distance, the classification being able to determine the state of a cell among predetermined states. The processor may be a microprocessor, connected to a programmable memory, having a sequence of instructions for carrying out the steps described in this description. Preferably, the device has no magnification optics between the photodetector and the sample analyzed. According to one embodiment, the processor is able to determine said characteristic quantity at a plurality of reconstruction distances along said propagation axis, the classification being carried out as a function of the evolution of said characteristic quantity along said propagation axis. The sample may be disposed in a transparent enclosure, placed between the photodetector and the light source. An object of the invention is also an incubator for cell growth comprising a device as previously described. FIGURES FIG. 1 represents the device according to one embodiment of the invention. FIG. 2 represents an image acquired by the photodetector according to a first exemplary embodiment. FIGS. 3A to 3C show, for a first exemplary embodiment, images of the phase of the light wave incident on the detector, these images coming from a holographic reconstruction at three different reconstruction distances. FIGS. 4A and 4B respectively represent, for a first exemplary embodiment, the profile of the phase and the profile of another characteristic quantity, called complementary amplitude, along the axis of propagation, and that for 5 cells. FIGS. 5A and 5B respectively represent, for a second exemplary embodiment, the profile of the phase and the profile of another characteristic quantity, called complementary amplitude, along the axis of propagation, for a plurality of cells .
    [0004] FIGS. 6A and 6B show respectively, for a third exemplary embodiment, the profile of the phase and the profile of another characteristic quantity, called complementary amplitude, along the axis of propagation, and this for a plurality of cells. FIG. 7 represents, in connection with this third exemplary embodiment, the profile of a composite magnitude combining phase and absorption along the propagation axis for a plurality of cells. DESCRIPTION OF PARTICULAR EMBODIMENTS FIG. 1 represents an exemplary device that is the subject of the invention. A light source 11 10 is able to produce a light wave 12, called the incident light wave, in the direction of a sample 14, along an axis of propagation Z. The sample 14 comprises a culture medium 6 as well as cells 1 , 2, 3, 4, 5 which one wishes to determine the state, and in particular if they are alive or dead. The distance 4 between the light source and the sample is preferably greater than 1 cm.
    [0005] It is preferably between 2 and 10 cm, typically 5 cm. Preferably, the light source, seen by the sample, is considered as point. This means that its diameter (or diagonal) must be less than one fifth, better one-tenth of the distance between the sample and the light source. Thus, the light arrives at the sample in the form of plane waves, or can be considered as such.
    [0006] The light source 11 may be punctual, or be associated with a diaphragm, not shown in FIG. 1, so as to appear punctually. The opening of the diaphragm is typically between 50 μm and 1 μm, preferably 50 μm and 500 μm. The diaphragm may be replaced by an optical fiber having a first end facing a light source and having a second end facing the sample. In this case, said second end can be likened to a point light source 11. The sample 14 is delimited by an enclosure having a bottom 15 and a cover 13. The side walls of the enclosure are not shown. Typically an enclosure is a petri dish or the well of a well plate. In the example under consideration, the bottom 15 and the cover 13 consist of 2 transparent blades 100 μm apart. The distance d between the cells 1,2,3,4,5 and the photodetector 16 is equal to 3450 μm.
    [0007] In general, the thickness of the enclosure, along the axis of propagation Z, is preferably less than a few cm, for example less than 5 cm, or even less than 1 cm. The light source 11 may be temporally coherent but this is not necessary. In this example, the light source is an OSRAM light emitting diode, reference LA LA E67B-U2AA-24-1. It is located at a distance 4 equals 5 cm from the sample. The sample 14 is disposed between the light source 11 and a matrix photodetector 16. The latter extends along a detection plane P, preferably parallel or substantially parallel to the bottom 15 of the enclosure delimiting the sample. The detection plane P preferably extends perpendicularly to the axis of propagation Z.
    [0008] The term substantially parallel means that the two elements may not be strictly parallel, an angular tolerance of a few degrees, less than 10 ° being allowed. Preferably, the light source is of small spectral width, for example less than 200 nm, or even 100 nm or even 25 nm. The term spectral width refers to the width at half height of the emission peak of the light source. The photodetector 16 may be a matrix photodetector comprising a matrix of pixels, of the CCD type or a CMOS. CMOS are the preferred photodetectors because the size of the pixels is smaller, which makes it possible to acquire images whose spatial resolution is more favorable. In this example, the detector is a 12-bit APTINA sensor, reference MT9P031. This is a CMOS RGB sensor, whose inter pixel pitch is 2.2 μm. The effective area of the photodetector is 5.7 x 4.3 mm 2. The photodetectors whose inter pixel pitch is less than 3 μm are preferred because they make it possible to obtain images with a satisfactory spatial resolution. Preferably, the photodetector comprises a matrix of pixels, over which is disposed a transparent protective window. The distance between the pixel matrix and the protection window is generally between a few tens of μm to 150 or 200 μm. In general, and irrespective of the embodiment, the distance d between a particle and the pixels of the photodetector is preferably between 50 μm and 2 cm, preferably between 100 μm and 2 mm.
    [0009] The absence of magnification optics between the matrix photodetector 16 and the sample 14 is noted. This does not prevent the possible presence of focusing microlenses at each pixel of the photodetector 16. In this first example, the culture medium is a DMEM medium (Dubelcco's Modified Eagle's Medium). The sample also contains Fibroblast 3T3 type cells, the concentration of which is approximately 0.5 10 6 cells per ml. FIG. 2 represents an image obtained by the photodetector 16. This figure represents a global diffraction figure, in which elemental diffraction patterns 31, 32, 33, 34, 35 are distinguished, each elementary diffraction pattern being respectively associated with the cells 1, 2, 3, 4 and 5. Each elemental diffraction figure comprises a disk-shaped central zone, around which concentric rings, alternately dark and light, extend. The area marked with the number 6 corresponds to a bottom area, not including a cell. Each elemental diffraction pattern (31, 35) is formed by the interference between the incident light wave 12 produced by the source 11, upstream of the sample, and a diffraction wave of this incident wave. produced by each cell (1, ..., 5). Thus, the photodetector 16 is exposed to a light wave 22 formed by the superposition of: - the incident light wave 12 emitted by the source 11, upstream of the sample 14, - the diffraction wave produced by each of the cells 1, .., 5 or other diffractive elements present in the sample. A processor 20 receives the images of the matrix photodetector 16 and performs a reconstruction of characteristic quantities of the light wave 22 to which the photodetector is exposed, along the propagation axis Z. The reconstruction is carried out in particular between the photodetector and the observed sample.
    [0010] The processor 20 may be able to execute a sequence of instructions stored in a memory, for carrying out the steps of the identification method. The processor may be a microprocessor, or any other electronic computer capable of processing the images provided by the matrix photodetector, to execute one or more steps described in this description.
    [0011] The image shown in FIG. 2 corresponds to the intensity distribution I (x, y), where x and y designate the coordinates in the detection plane P previously described.
    [0012] According to the well-known principles of digital holographic reconstruction, described in Ryle et al., "Digital in-line holography of biological specimens", Proc. Of SPIE Vol.6311 (2006), by carrying out a product of convolution between the intensity 1 (x, y) measured by the photodetector, and a propagation operator h (x, y, z), it is possible to reconstruct a Complex expression U (x, y, z) of the light wave 22 at any coordinate point (x, y, z) of the space, and in particular in a plane at a distance I z I of the photodetector, and parallel to the plane P along which the photodetector extends. The propagation operator h (x, y, z) has the function of describing the propagation of light between the photodetector 16 and a coordinate point (x, y, z). It is then possible to determine the amplitude u (x, y, z) and the phase (p (x, y, z) of this light wave 22 at this distance I z I, called the reconstruction distance, with: u (x, y, z) = abs [U (x, y, z)] - (p (x, y, z) = arg [U (x, y, z)] The operators abs and arg respectively denoting the module and the argument.
    [0013] In particular, the application of the propagation operator makes it possible to determine the complex expression U (x, y, z) at a distance I z I of the photodetector, upstream of the latter. The complex value of the light wave 22 is then reconstructed before the latter reaches the detector. This is called back propagation. By assigning the coordinate z = 0 to the detection plane P, this backpropagation is implemented by applying a propagation operator h (x, y, - I z I). The terms upstream and downstream are to be understood according to the direction of propagation of the incident wave (12). If 1 (x, y) = I (x, y, z = 0) corresponds to the intensity of the signal measured by the photodetector, a relation between the measured intensity 1 (x, y) and the complex expression of the The light wave U (x, y) at the detection plane P is given by: / (x, y) = IU (x, y) I2. The complex expression of the light wave (22) at a coordinate (x, y, z) is given by U (x, y, z) = .1 / (x, y) * h (x, y, z), the symbol * denoting a convolution product. with: - z <0 in the half-space delimited by the detection plane P, comprising the sample 14, 3034197 9 - z> 0 in the half-space delimited by the detection plane P and not including the sample 14. In the half-space delimited by the detection plane P and comprising the sample 14, the complex expression of the light wave can also be written: 5 U (x, y, z) = .11 (x , y) * h (x, y, -IzI) Preferably a mathematical preprocessing is previously applied to the measured intensity 1 (x, y) before the holographic reconstruction. This improves the quality of results, including reducing artifacts when applying the propagation operator.
    [0014] Thus, we determine an intensity i (x, y), called normalized intensity, such that i (x, = (/ (x, - Average (0) / Average (I) with - 1 (x, y) = intensity measured by the photodetector at the (x, y) coordinate, - Average (I) = average of the intensity measured in a region of interest of the image I, including said coordinate (x, y). The interest may correspond to the entire image formed by the photodetector This preprocess is similar to a normalization of the intensity measured by the intensity of the incident light wave 12, the latter being estimated by the average magnitude ( I) It limits the artifacts generated by the reconstruction process.
    [0015] The digital reconstruction can in particular be based on the Fresnel diffraction model. In this example, the propagation operator is the Fresnel-Helmholtz function, such that: 12.1 2 + 3/2 h (x, y, z) = A -z e eexp (j7r -Az). where X denotes the wavelength.
    [0016] 2 Thus, U (x, y, z) ze-12n-7, ff, y ') expUlr (x-x') + (31-31'2)) dx'dy 'Az 25 where - x' and y 'designate the coordinates in the plane of the photodetector, - x and y denote the coordinates in the reconstruction plane, the latter being situated at a distance Izi from the photodetector, z represents the coordinate of the image reconstructed along the axis of propagation Z of the incident light wave 12. From the values of the complex expression U (x, y, z), it is possible to extract characteristic quantities of the light wave 22 resulting from the diffraction, by the particles (1,2.9), of the 5 of the incident light wave 12 emitted by the source 11. As previously mentioned, it is possible to evaluate the amplitude u (x, y, z) or the phase (p (x , y, z), but it is also possible to evaluate any function of the amplitude or of the phase, for example, a characteristic quantity, called complementary amplitude, ft (x, y, z) such that : 10 ft (x, y, z) = abs (1 - U (x, y, z)) From each reconstructed complex expression U (x, y, z), it is possible to constitute: an image uz of the amplitude of the wave 22, in a plane parallel to the plane of the detector, to a distance I z I of the latter, with uz (x, y) = abs [U (x, y, z)], an image (pz of the phase of the wave 22, in a plane parallel to the plane of the detector at a distance I z I of the latter, with (pz (x, y) = arg [U (x, y, z)], an image ri; of the complementary amplitude, as previously defined, of the wave 22, in a plane parallel to the detector plane, at a distance I z I of the latter, with IT; (x, y, z) = abs [1 - U (x, y, z)]. FIGS. 3A to 3C respectively represent images (pz of the phase reconstructed in planes parallel to the matrix photodetector, with I zI = 3050 pm, I z I = 3450 pm (z = d) and I z I = 3850 pm respectively). , knowing that the cells are located in the plane I z I = 3450 pm We observe, on each image (pz reconstructed, an elementary diffraction pattern (31, 32, 33, 34, 35) corresponding to each cell (1,2 , 3,4,5) of the sample, the central part of each figure making it possible to determine the respective coordinates (xi, yi), (x2, y2), (x3, y3), (x4, y4) and ( xs, ys) cells 1 to 5 in the detection plane P. The value of the phase (p (xi, yi, z), (p (x2, y2, z), p (x3, y3, z), (p (x4, y4, z), (p (xs, ys, z) at the different z values considered: at I z I = 3850 pm, the phase associated with each cell is positive, with a value close to 7C / 5, at I z I = 3450 pm (z = d), the phase associated with cells 1, 2 and 3 is negative (see sine of 30-7C / 5), while the phase associated with the cells 4 and 5 is positive (close to + 7C / 5), at 30Z19 = 3050 um, the phase associated with each cell is negative, of value close to - 'TC / 5. Thus, on the plane I z I = 3450 μm, corresponding to the plane in which the cells (z = d) are actually located, the phase of the reconstructed light wave 22 passing respectively through the cells 1, 2 and 3, is negative, while the phase of the reconstructed light wave 22, passing respectively by the cells 4 and 5 is negative. Moreover, following these reconstructions, the trypan blue cells were stained and then observation using a microscope, using 10x magnification. Trypan blue is a dye commonly used in the field of cell viability. The cells labeled 1, 2 and 3 appear alive, whereas the cells labeled 4 and 5 have a dark spot, indicating cell death. These observations serve as a reference measure in the analyzes detailed below. By reconstructing an image of the radiation to which the detector is exposed on the plane containing the cells (z = 3450 μm), and by identifying, on this reconstructed image, the position of each cell, it is possible to discriminate living cells (negative phase) dead cells (positive phase). FIG. 4A illustrates, for each cell n (1 n 5), the evolution of the profile (p (x ,,, yr ,, z) of the phase as a function of z, for I z I between 3000 μm and 4000 μm. The profiles corresponding to living cells (n = 1, 2 and 3) are distinguished by a marked slope at I <3450 μm, whereas the profiles corresponding to dead cells (n = 4 or 5) are distinguished by a progressive decrease of the phase along the axis of propagation Z, in the direction from the matrix photodetector to the sample, so that it is possible to establish a profile representing the evolution of the phase of wave 22 at which 25 is exposed along an axis, parallel to the axis of propagation Z, passing through each cell, this profile can then be used to perform a classification between a living cell and a dead cell, this profile can in particular be compared with a library of profiles made on "standard" cells whose state is known. nt said, the profile representing the evolution of the phase along the axis of propagation of the light wave is a signature 30 of the state of the cell. The fact of reconstructing a characteristic quantity of the wave 22 resulting from the diffraction of a particle with the incident wave 12 not at a single reconstruction distance, but along the axis of propagation of the wave 3034197 12 incident at a plurality of reconstruction distances, provides richer information. This allows a reliable classification between the different states of a cell. Moreover, this avoids knowing precisely the distance separating a cell to be characterized from the photodetector.
    [0017] Another indicator may be the distance I zo at which the phase value (p (xo, yn, z) goes through zero, a cell being considered alive if Izol is less than the distance d actually separating the cell from the photodetector (in the occurrence d = 3450 μm), and dead in the opposite case Figure 4B represents for each cell n (1 n 5), the evolution of the profile ft (xn, yn, z) of the complementary amplitude in The profiles corresponding to the living cells (n = 1, 2 and 3) are distinguished by a minimum value of min 50, whereas for dead cells the value of z is between 3000 and 4000 μm. The minimum profile ft min is greater than 50. In other words, it is possible to define a threshold value j ".. i thresholdr the comparison of this threshold value j" .. i threshold with a remarkable point of the profile, in this case the minimum value, which makes it possible to classify the cell as alive or as dead. Note also that when the cells are alive, the minimum value ft min of the profile is reached at I <3450 um, which is not the case of dead cells. In other words, it is possible to identify the position zmin, along the axis of propagation Z, of a remarkable point of the profile, in this case a minimum, and to compare this position at the distance d between the analyzed cell and the photodetector. If I zmin d, the cell is considered viable. Otherwise, it is considered dead. It is therefore possible to establish a profile representing the evolution of the complementary amplitude ft of the light wave 22 to which the detector is exposed, along the axis of propagation Z and passing through each cell, and to use this profile to perform a classification between a living cell and a dead cell. This profile can in particular be compared to a library of profiles made on "standard" cells whose state is known. In other words, the profile representing the evolution of the complementary amplitude ft along the axis of propagation constitutes a signature of the state of the cell.
    [0018] In a second example, the device is similar to that previously implemented. The cells characterized are PC12 cells. As in the first previous example, an image was acquired on the matrix photodetector, in a configuration identical to that shown in FIG. 1. This image allowed the reconstruction of a complex expression U (x, y, z) of the wave 22, to which the photodetector is exposed, along the axis of propagation Z, the reconstruction distance varying from 3000 μm to 3800 μm. A reference measurement was then performed, using Trypan blue labeling, to identify dead D cells of living cells A. Figure 5A shows the evolution of the phase (p (xo, yn, z) ) as a function of 1z1, (xn, yn) denoting the coordinates of the center of each examined cell n, As in the previous example, it is observed that: the phase (p (xo, yo, 1z1 = d = 3450 um ) is negative for living cells, and positive or zero for dead cells, the profile (p (xo, yn, z) associated with each living cell is distinguished by a marked decay of the phase at 1 zl <d, while that the profile (p (xo, yn, z) associated with each dead cell is distinguished by a slower evolution of the profile as a function of z. The profile representing the evolution of the phase along the axis of propagation Z therefore constitutes a 15 signature of the state of the cell - the value Izo 1 at which the phase of the reconstructed wave 22 is equal to 0 varies according to the state of the cells: I zo l <d for living cells, I zo 1 d for dead cells. There are thus 3 criteria for classifying a cell: value of the phase at Iz 1 = d, evolution of the phase as a function of z and value Izo 1 at which the value of the phase of the complex expression of the reconstructed wave 22 is zero. FIG. 5B represents the evolution of the complementary amplitude ft (xo, yn, z), as previously defined, as a function of z, (xn, yn) designating the coordinates of the center of each characterized n cell. As in the previous example, the evolution of the profile of the complementary amplitude is different depending on whether the cell is alive or dead. In particular, when the minimum value ft, 'o of the profile is less than a threshold value j ".. i .., .. threshoid, here of the order of 100, a cell is declared alive, and dead in the case In a third example, the device is similar to that previously used, the characterized cells being CHO (Chinese hamster ovary cell line cells derived from Chinese hamster ovaries). two previous examples, we acquired an image on the matrix photodetector, in a configuration identical to that shown in Figure 1. This image has allowed the reconstruction of a complex expression U (x, y, z) of the wave 22, to which the photodetector is exposed, along the axis of propagation Z, the reconstruction distance I ranging from 3000 μm to 3800 μm.A reference measurement was then carried out, using a Trypan blue marking. , 5 to identify cellu D. Deaths and living cells A. FIG. 6A shows the evolution of the phase (p (xo, yn, z) as a function of z, (xn, yn) designating the coordinates of the center of each characterized n cell. As in the previous example, it is observed that: the phase (p (xo, yo, I) = d = 3450 μm) is negative for living cells, and positive for dead cells, the profile ( p (xo, yn, z) associated with each living cell is distinguished by a marked decay of the phase at Izl <d, while the profile (p (xo, yn, z) associated with each dead cell is distinguished by an evolution The profile representing the evolution of the phase along the axis of propagation Z therefore constitutes a signature of the state of the cell, the value I zo at which the phase of the wave 22 is equal to 0 varies depending on the state of the cells: I zo I <d for living cells, I zo I> d for dead cells Figure 6B shows the evolution of the complementary amplitude, (xo, yn, z) as previously defined, as a function of z, (xn, yn) designating the coordinates of the center of each n-cell characterized. that in the previous example, the evolution of the profile of the complementary amplitude is different depending on whether the cell is alive or dead. In particular, when the minimum value ft, o of the profile is less than a threshold value of 30 hr, here 30, a cell is declared alive, or dead in the opposite case.
    [0019] According to one variant, the classification between a living cell and a dead cell is carried out by combining, for a given height z, different parameters of the light radiation 22 to which the detector is exposed. According to one example, the phase (p (x, y, z) and the complementary amplitude ft (x, y, z) along the propagation axis Z are determined, the classification being carried out using the ratio between these two parameters.
    [0020] FIG. 7 represents the profile, along the axis of propagation Z, of the composite quantity k (x, y, z) such that k (x, y, z) = (p (x, y, z) k) (x6, y6, z) (x, y, z) (p (x, y, z) The term k (x6, y6, z) representing the ratio determined in part 6 of the sample "ii (x, y, z) free of cell This ratio can be called reference ratio.
    [0021] This figure shows the evolution of the composite quantity k (x ,,, y ,,, z) for n cells, each cell n being identified by its position (xn, yn) in the plane of the photodetector. The value of the composite quantity, at a determined z reconstruction distance, is systematically higher for living cells than for dead cells. It is then possible to define a threshold kthreshold (Z), such that if k (x ,,, y ,,, z) kthreshold (z), the cell centered on the position (xn, yn), in the plane P is alive, or dead in the opposite case. The examples described above expose simple identification criteria, based on the evolution of the profile of a characteristic quantity as a function of the reconstruction distance, and comparisons using pre-established thresholds. Naturally, other, more complex, classification methods can be implemented without departing from the scope of the invention.
    权利要求:
    Claims (15)
    [0001]
    REVENDICATIONS1. A method for determining the state of a cell (1,2,3,4,5), said cell being placed in a sample (14), the method comprising the steps of: illuminating said sample with a light source (11), the light source producing an incident light wave (12) propagating towards the sample (14) along an axis of propagation (Z), acquisition, using a matrix photodetector (16). ) an image (I) of the sample, the sample being disposed between said light source and said matrix photodetector, such that the matrix photodetector is exposed to a light wave (22) comprising interference between the incident light wave (12) and a diffraction wave produced by each cell (1,2,3,4,5), identifying a position (xn, yn) of said cell in a plane parallel to a detection plane ( P) according to which the matrix photodetector extends, application of a reconstruction algorithm n digital to said acquired image (I), so as to determine at least one characteristic magnitude (u, cp, ft, k) of said light wave (22) to which the photodetector is exposed, at a distance (lz1) thereof last, said reconstruction distance, along said propagation axis (Z), classification of said cell as a function of the value of said characteristic quantity, at said position (xn, yn), and at said reconstruction distance, the classification allowing determining the state of said cell from predetermined states.
    [0002]
    The method of claim 1, wherein the predetermined states comprise a cellular state of life and a cell death state.
    [0003]
    3. A method according to any one of the preceding claims, wherein the characteristic quantity is obtained by estimating, at said reconstruction distance, a complex expression (U (x, y, z)) of the light wave (22) to which is exposed the matrix photodetector.
    [0004]
    The method of claim 3, wherein said characteristic quantity is determined from the module or argument of said complex expression (U (x, y, z)). 3034197 17
    [0005]
    A method according to any one of the preceding claims, wherein said characteristic quantity is determined at a plurality of reconstruction distances along said propagation axis (Z), the classification being carried out as a function of the evolution of said characteristic magnitude. along said propagation axis. 5
    [0006]
    The method of claim 5, wherein the classification is performed by comparing said evolution of said characteristic quantity with predetermined standard profiles.
    [0007]
    A method according to any one of the preceding claims, further comprising a step of reconstructing an image of said characteristic quantity in a plane parallel to the detection plane (P), and at said reconstruction distance, the value of said characteristic magnitude at said position (xn, yn) of the cell at said reconstruction distance, being determined according to this image. 15
    [0008]
    8. The method of claim 7, the position (xn, yn) of each cell in a plane parallel to the detection plane (P) being determined using the image thus reconstructed.
    [0009]
    9. A method according to any one of the preceding claims, the light source (11) being a spatially coherent source. 20
    [0010]
    The method of any of the preceding claims, wherein the light source (11) is a light emitting diode.
    [0011]
    The method of any of the preceding claims, wherein no magnification optics are disposed between the sample (14) and the matrix photodetector (16).
    [0012]
    12. A device for determining the state of a cell, said cell being disposed in a sample, the device comprising: a light source (11) arranged to produce an incident light wave (12) along an axis of propagation ( Z), in the direction of said sample (14), a matrix photodetector (16), arranged to acquire an image of the sample, by being exposed to a light wave (22), resulting from the interference between said light wave incident (12) and a diffraction wave formed by said cell, a support, for holding the sample between said light source (11) and the matrix photodetector (16), the device being characterized in that it comprises a processor (20) configured to implement the following steps: - identification of a position (xn, yn) of said cell in a plane parallel to a plane along which the photodetector extends, application of a reconstruction algorithm digital to said acquired image, so as to determine at least one characteristic quantity (u, cp, ft, k) of the light wave (22) to which the photodetector is exposed, at a distance (1z1) from the latter, said distance of reconstruction, according to the axis of propagation (Z) classification of said cell as a function of the value of said characteristic quantity, 15 to said position (xn, yn), and to said reconstruction distance, the classification being suitable for determine the state of a cell among predetermined states
    [0013]
    The device of claim 12, wherein the device has no magnification optics between the matrix photodetector (16) and the analyzed sample (14).
    [0014]
    14. Device according to one of claims 12 to 13, wherein said processor (20) is adapted to determine said characteristic quantity at a plurality of reconstruction distances, according to said axis of propagation (Z), the classification being performed according to the evolution of said characteristic quantity along said propagation axis
    [0015]
    15. Incubator for cell growth, the incubator comprising at least one device according to claims 12 to 14.
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    同族专利:
    公开号 | 公开日
    EP3274694A1|2018-01-31|
    WO2016151249A1|2016-09-29|
    FR3034197B1|2020-05-01|
    US20180113064A1|2018-04-26|
    US10481076B2|2019-11-19|
    EP3274694B1|2019-12-18|
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    2016-03-31| PLFP| Fee payment|Year of fee payment: 2 |
    2016-09-30| PLSC| Publication of the preliminary search report|Effective date: 20160930 |
    2017-03-31| PLFP| Fee payment|Year of fee payment: 3 |
    2018-03-29| PLFP| Fee payment|Year of fee payment: 4 |
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    2021-12-10| ST| Notification of lapse|Effective date: 20211105 |
    优先权:
    申请号 | 申请日 | 专利标题
    FR1552445A|FR3034197B1|2015-03-24|2015-03-24|METHOD FOR DETERMINING THE STATE OF A CELL|
    FR1552445|2015-03-24|FR1552445A| FR3034197B1|2015-03-24|2015-03-24|METHOD FOR DETERMINING THE STATE OF A CELL|
    PCT/FR2016/050644| WO2016151249A1|2015-03-24|2016-03-23|Method for determining the state of a cell|
    EP16714496.3A| EP3274694B1|2015-03-24|2016-03-23|Method for determining the state of a cell|
    US15/560,694| US10481076B2|2015-03-24|2016-03-23|Method for determining the state of a cell|
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