# US 2014/0193850 A1 · Holographic method and device for cytological diagnostics > Agents: this data is available as JSON from the patentgrep API and MCP server — see https://patentgrep.com/llms.txt - Number: US 2014/0193850 A1 - Document ID: US20140193850A1 - Status: Published application - Kind: A1 - Application number: 14/233,580 - Filed: 2012-07-16 - Published: 2014-07-10 - Earliest claimed: 2011-07-19 - Assignees: Ovizio Imaging Systems NV/SA - Inventors: Serge Jooris; Philip Mathuis - Web page: https://patentgrep.com/patent/US20140193850A1 ## CPC - G01N 21/453: {Holographic interferometry (for dimensional measurements G01B9/021 - G01B9/029)} - G03H 1/0866: {Digital holographic imaging, i.e. synthesizing holobjects from holograms} - G06F 16/24573: {using data annotations, e.g. user-defined metadata} - G06V 20/693: {Acquisition} - G03H 1/0443: {Digital holography, i.e. recording holograms with digital recording means (holobject computation G03H1/0866)} - G03H 2001/005: {in microscopy, e.g. digital holographic microscope [DHM]} - G03H 2001/0445: {Off-axis recording arrangement (G03H2001/0456 takes precedence)} - G03H 2001/0447: {In-line recording arrangement} - G01N: INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES (measuring or testing apparatus or processes other than immunoassay, involving enzymes or microorganisms C12M, C12Q) - G03H: HOLOGRAPHIC PROCESSES OR APPARATUS (holograms, e.g. point holograms, used as ordinary optical elements G02B5/32; producing stereoscopic or other three-dimensional effects G02B30/00; diffraction-grating systems G02B27/44; systems using moiré fringes G02B27/60; optical logic elements G02F3/00; stereo-photography G03B35/00; photosensitive materials or processes for photographic purposes G03C; {stereo-photographic or similar processes G03C9/00}; apparatus for processing exposed photographic materials G03D; analogue computers performing mathematical operations with the aid of optical elements G06E3/00; authentication by radiation, of concealed information carried by holograms or diffraction gratings G06K19/16; holographic storage G11B7/0065, G11C13/04; {stereoscopic or other three dimensional effects in television systems H04N13/00}) - G06F: ELECTRIC DIGITAL DATA PROCESSING (computer systems based on specific computational models G06N) - G06V: IMAGE OR VIDEO RECOGNITION OR UNDERSTANDING ## Abstract The present invention discloses a method for analyzing a liquid cell sample, comprising the steps of: a) providing at least one liquid cell sample in a sample vial; b) obtaining data linked to the cells in the sample by performing differential digital holographic microscopy on said liquid cell sample in said sample vial. In a second aspect, the invention also provides for a system for analyzing a liquid cell sample, comprising (i) a differential digital holographic microscope comprising illumination means, a differential interferometer and a digital recording device connected to a processing device such as a computer; (ii) at least one exchangeable sample vial comprising a liquid cell (iii) a movable sample vial holder; characterized in that (iv) said sample vial holder is adapted to receive said sample vial; (v) said sample vial holder is adapted to position said sample vial such that the focal plane of the objective lens of said differential digital holographic microscope lies in the vial. ## Claims ### Claim 1 A method for analyzing a liquid cell sample, comprising the steps of: a) providing at least one liquid cell sample in a sample vial; b) obtaining data linked to the cells in the sample by performing differential digital holographic microscopy with a differential interferometer on said liquid cell sample in said sample vial, whereby cells in said liquid cell sample are suspended in a solution whereby said solution comprises an anti-clumping agent. ### Claim 2 (depends on 1) Method according to claim 1, whereby said cells comprise a tissue sample, a biopsy sample, a brushing or scraping sample from oral cavities, nipple secretions, skin lesions, eye brushings, a fine-needle-aspiration sample, a smear sample, a mucoid specimens taken from respiratory or gastrointestinal tracts or body fluids such as serous effusions or urinary or cerebrospinal fluids. ### Claim 3 (depends on 1) Method according to claim 1, whereby said solution comprises a buffering component and an alcohol. ### Claim 4 (depends on 1) Method according to claim 1, whereby obtaining said data, comprises the steps of c) illuminating in transmission and/or in reflection with illumination means said liquid cell sample and producing thereby a sample beam, whereby said illumination means preferably comprise spatially and temporally partially coherent light. ### Claim 5 (depends on 4) Method according to claim 4, comprising the steps of: d) generating by means of the differential interferometer interfering beams from said sample beam; e) adequately positioning and orientating the tilting means in the second interferometer arm (respectively in the first interferometer arm) for tilting the beam reflected by the second reflecting element (respectively first reflecting element) relatively to the beam reflected by the first reflecting element (respectively the second reflecting element) by a precise tilting angle in such a way to superpose the beam reflected by the first reflecting element (respectively the second reflecting element) and the beam reflected by the second reflecting element (respectively the first reflecting element) in the front focal planes of the focusing means thereby creating a precise shift between the interfering beams reflected and transmitted by the second beam splitter on the sensor of the electronic imaging device; f) detecting and recording the fringe interference image thus formed by the interfering beams on the sensor of the imaging device; g) sending the interference image to processing means, such as a computer; h) possibly acquiring other similar but different interference images following steps c-g from said sample by implementation of the phase-stepping method; i) processing said interference image(s) so as to extract the optical amplitude and/or phase of the sample by implementation of the phase stepping method or the Fourier transform data processing; and j) computing said data linked to the cells in the sample from said optical amplitude and/or phase of said liquid cell sample. ### Claim 6 (depends on 5) Method according to claim 5, comprising the steps of: k) providing at least once a test sample in a test sample vial; l) illuminating in transmission and/or in reflection with illumination means said test sample and producing thereby a test sample beam, whereby said illumination means preferably comprise spatially and temporally partially coherent light; m) generating by means of the differential interferometer interfering beams from said test sample beam; n) adequately positioning and orientating the movable part of the interferometer so as to equalize the optical length of said interfering beams with an accuracy in the range of less than the maximum wavelength of the illumination means to a few maximum wavelengths by means of the moving means. ### Claim 7 (depends on 1) Method according to claim 1, whereby said data comprises cell density, cell morphology, cell size, the ratio between nucleus and cytoplasm of a cell and/or the optical density of a cell present in the said liquid cell sample. ### Claim 8 (depends on 1) Method according to claim 1, whereby said data obtained by differential digital holographic microscopy are compared and correlated with a reference database comprising a set of cellular parameters. ### Claim 9 (depends on 8) Method according to claim 8, whereby a digital report and image of said liquid cell sample is created based upon said data obtained by digital holographic microscopy and said correlation of said data with reference database of known cellular parameters. ### Claim 10 (depends on 1) Method according to claim 1, whereby providing said at least one liquid cell sample in a sample vial comprises the steps of: o) placing at least one sample vial with a liquid cell sample in a movable sample vial holder; p) positioning said sample vial holder with said sample vial such that said liquid cell sample can be illuminated by said illumination means. ### Claim 11 (depends on 10) Method according to claim 10 wherein the sample vial thickness is larger than the positioning precision of the movable sample vial holder and the sample vial holder is placed such that the focal plane of the objective lens of the differential digital holographic microscope lies in the vial. ### Claim 12 (depends on 1) Method according to claim 1, whereby at least 20% of the cells in said liquid cell sample are single cells. ### Claim 13 (depends on 1) Method according to claim 1, comprising the step of shaking said sample, preferably prior to and/or during the step of obtaining said data by performing differential digital holographic microscopy. ### Claim 14 A system for analyzing a liquid cell sample, comprising: (i) a differential digital holographic microscope comprising illumination means, a differential interferometer and a digital recording device connected to a processing device such as a computer; (ii) at least one exchangeable sample vial comprising a liquid cell sample, wherein cells are suspended in a solution whereby said solution comprises an anti-clumping agent; (iii) a movable sample vial holder; characterized in that (iv) said sample vial holder is adapted to receive said sample vial; (v) said sample vial holder is adapted to position said sample vial such that the focal plane of the objective lens of said differential digital holographic microscope lies in the vial. ### Claim 15 (depends on 14) System according to claim 14, whereby said sample vial comprises a material which is transparent for the illumination beam of said illumination means, or said sample vial has identifying indicia, preferably fixed indicia or programmable indicia. ### Claim 16 (depends on 14) System according to claim 14, comprising a data processing unit, a computer or an electronic device which is capable of performing an algorithm to compare data obtained by said differential digital holographic microscope with a reference database of cellular parameters. ### Claim 17 (depends on 16) System according to claim 16, comprising a computer or printer capable of providing a report based on the comparison of said data and said reference database, whereby said report is correlated with said indicia on said sample vial.