# US 2022/0034812 A1 · Optical arrangment for fluorescence microscopy applications > Agents: this data is available as JSON from the patentgrep API and MCP server — see https://patentgrep.com/llms.txt - Number: US 2022/0034812 A1 - Document ID: US20220034812A1 - Status: Published application - Kind: A1 - Application number: 17/275,704 - Filed: 2019-09-12 - Published: 2022-02-03 - Earliest claimed: 2018-09-18 - Assignees: Fraunhofer-Gesellschaft Zur Foerderung Angewandten Forschung E.V.; Friedrich-Schiller-Universitaet Jena - Applicants: Fraunhofer-Gesellschaft Zur FöRderung Der Angewandten Forschung E.V.; Friedrich-Schiller-Universitaet Jena - Inventors: Markus GRAEFE; Marta GILABERTE BASSET; Falk EILENBERGER; Frank SETZPFAND - Web page: https://patentgrep.com/patent/US20220034812A1 ## CPC - G01N 21/6458: {Fluorescence microscopy (fluorescence microscopes per se G02B21/0076 and G02B21/16)} - G02B 21/0076: {arrangements using fluorescence or luminescence} - G02B 21/367: {providing an output produced by processing a plurality of individual source images, e.g. image tiling, montage, composite images, depth sectioning, image comparison} - G02B 27/58: Optics for apodization or superresolution; Optical synthetic aperture systems - 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) - G02B: OPTICAL ELEMENTS, SYSTEMS OR APPARATUS ## Abstract An optical arrangement for fluorescence microscopy applications. Electromagnetic radiation from a radiation source is directed onto a biological sample in the form of a light sheet. One of more fluorophore(s) is contained in the sample. The radiation photoactivates the fluorophore(s) by exciting them from a state which they cannot be exited to fluoresce to a state which they can be exited to fluoresce by illuminating with electromagnetic radiation of a particular wavelength, and subsequently photodeactivating them. Multiphoton beams of nonclassical light are directed onto a first optical system the beam(s) are directed onto a sample of the light sheet. Fluorescent radiation of fluorophores, can be excited within the light sheet by the plurality of multiphoton beams occurring simultaneously on/in the sample. The fluorescence radiation occurs by means of a second optical system on a detection system which measures in a spatially resolving manner. ## Claims ### Claim 1 An optical arrangement for fluorescence microscopy applications, in which electromagnetic radiation from a radiation source is directed onto a biological sample in the form of a light sheet and one or more fluorophores are contained in the sample, wherein the electromagnetic radiation photoactivates the fluorophore(s) by exciting them from a state in which they cannot be excited to fluoresce into a state in which they can be can be excited to fluoresce by illumination with electromagnetic radiation of a particular wavelength and subsequently photodeactivating them from a state in which they can be excited to fluoresce into a state in which they cannot be can be excited to fluoresce by illumination with electromagnetic radiation of another particular wavelength, one or more multiphoton beams, and at least one or two photon pair beams are directed from a source of non-classical light onto a first optical system consisting of an arrangement of at least one optical lens or photon reflecting element or polarizing optical element, or optical filter or a combination thereof, and directed, from there to a sample in the region of the light sheet, such that fluorescence radiation of the one fluorophore or the fluorophores in the state in which they can be excited to fluoresce is excited with the several multiphoton beams incident simultaneously on/in the sample by means of multiphoton absorption within the light sheet, and fluorescence radiation obtained by excitation is incident, by means of a second optical system, on a detection system which is designed for spatially resolved detection of fluorescence radiation. ### Claim 2 (depends on 1) The arrangement according to claim 1, wherein the source of nonclassical light is a nonlinear crystal pumped by a laser or waveguide structure in a nonlinear crystal, or at least two identical coherently pumped quantum dots. ### Claim 3 (depends on 1) The arrangement according to claim 1, wherein the one or more multiphoton beams, but the at least one or more photon pair beams in collinear geometry, are directed towards the first optical system. ### Claim 4 (depends on 1) The arrangement according to claim 1, wherein the fluorescence radiation can be excited with two photons in the form of a photon pair. ### Claim 5 (depends on 1) The arrangement according to claim 1, wherein the radiation source emits at least two different wavelengths, at least one for photoactivation and at least one for photodeactivation, of the respective fluorophore(s). ### Claim 6 (depends on 1) The arrangement according to claim 1, wherein the radiation source is an optical system consisting of an arrangement of at least one optical lens or a photon reflecting element or a polarizing optical element, or an optical filter or a combination thereof. ### Claim 7 (depends on 1) The arrangement according to claim 1, wherein the formation of the light sheet is achieved by a movement of at least one optical element or an optical element increasing the beam cross-sectional area of the electromagnetic radiation onto which the electromagnetic radiation emitted by the radiation source is directed. ### Claim 8 (depends on 1) The arrangement according to claim 1, wherein the first optical system is used to linearly change the position of incidence of the at least one multiphoton beam on/in the sample, so that a corresponding line-shaped region of at least one line is irradiated at least once. ### Claim 9 (depends on 1) The arrangement according to claim 1, wherein a multiphoton beam emitted by the source is split into a plurality of partial beams and the partial beams are directed onto/into the sample by means of at least one first optical system for exciting fluorescence in the region of the light sheet. ### Claim 10 (depends on 1) The arrangement according to claim 1, wherein a plurality of partial beams are directed onto the sample to intersect one another on/in the sample. ### Claim 11 (depends on 1) The arrangement according to claim 1, wherein fluorescence can be excited simultaneously with a plurality of photon pair beams at a plurality of positions, or a single photon pair beam can be obtained with a plurality of photon pair beams combined with one another, and fluorescence can thus be excited point-by-point. ### Claim 12 (depends on 1) The arrangement according to claim 1, wherein a one- or two- or three-dimensional movement of the sample is performed for spatially resolved imaging of the sample. ### Claim 13 (depends on 1) The arrangement according to a claim 1, wherein the first optical system or the second optical system have a nonlinear optical crystal, an optical lens, a photon reflecting element, a polarization optics, an optical filter or an arrangement of a plurality of these optical elements. ### Claim 14 (depends on 1) The arrangement according to claim 1, wherein the detection system is a CCD, an EMCCD, an ICCD or a CMOS camera or a SPAD array.