Multi-Modal Fluorescence Imaging Flow Cytometry System
US-2024353309-A1 · Oct 24, 2024 · US
US9239456B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9239456-B2 |
| Application number | US-201214111759-A |
| Country | US |
| Kind code | B2 |
| Filing date | Apr 11, 2012 |
| Priority date | Apr 15, 2011 |
| Publication date | Jan 19, 2016 |
| Grant date | Jan 19, 2016 |
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A widefield microscope illumination system and a method for illumination, the system having a microscope objective with an optical objective axis, an illumination light source sending widefield illumination light along illumination beam paths having corresponding illumination axes along which the illumination light penetrates into the microscope objective through illumination light entry sites located within a predetermined illumination light entry area, a spatially resolving light detector detecting detected light sent from an illuminated sample through the microscope objective along a detected light beam path, and an automatic illumination light beam path manipulation device, controlled by a control system, which is arranged in front of the microscope objective in relation to the direction of the illumination light beam path, and by which illumination light beam path manipulation device the illumination axes are automatically movable at time intervals to a plurality of illumination light entry sites.
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What is claimed is: 1. A widefield microscope illumination system, wherein: the widefield microscope illumination system is adapted to be used for a localization microscope and further comprises; a microscope objective that comprises an optical objective axis; an illumination light source that sends widefield illumination light along illumination beam paths having corresponding illumination axes along which the illumination light penetrates into the microscope objective through illumination light entry sites located within a predetermined illumination light entry area of the objective; wherein an illumination beam cross section at the illumination light entry sites is smaller than the overall predetermined illumination light entry area of the objective; a spatially resolving light detector that detects detected light sent from an illuminated sample through the microscope objective along a detected light beam path; and an automatic illumination light beam path manipulation device, controlled by a control system, which is arranged in front of the microscope objective in relation to the direction of the illumination light beam path, and by means of which illumination light beam path manipulation device the illumination axes are automatically movable at time intervals to a plurality of different illumination light entry sites within the predetermined illumination light entry area. 2. The widefield microscope illumination system according to claim 1 , wherein the illumination axes always extend parallel to the objective axis. 3. The microscope illumination system according to claim 1 , wherein the illumination light beam path manipulation device comprises an optomechanical system, acousto-optical modulators (AOMs), or electro-optical modulators (EOMs), which establish an adjustable beam offset and thus an illumination light entry site that is adjustable with respect to the optical objective axis. 4. The microscope illumination system according to claim 1 , wherein the control system is configured in such a way that it automatically controls, according to a predefined pattern, a permitted adjustable beam offset in the region of the predetermined illumination light entry area for the illumination light into the objective, all the illumination light entry sites permitted by the control system being located within this predetermined illumination light entry area. 5. The microscope illumination system according to claim 1 , wherein the control system comprises a random generator that controls a permitted adjustable beam offset in the region of the predetermined illumination light entry area for the illumination light into the objective, all the illumination light entry sites permitted by the control system being located within this predetermined illumination light entry area. 6. The microscope illumination system according to claim 1 , wherein a control interface by means of which a control instruction adjusting the predetermined illumination light entry area can be entered. 7. The microscope illumination system according to claim 1 , wherein the predetermined illumination light entry area is a circular, circular-segment-shaped, annular, or annular-segment-shaped area. 8. The microscope illumination system according to claim 1 , wherein a measurement device that monitors the transmittance of the objective and sends a control signal to the control system when the transmittance falls below a predetermined threshold value. 9. A widefield illumination method for illuminating samples viewed with a microscope, the microscope comprising: a microscope objective that comprises an optical objective axis; and an illumination light source that sends widefield illumination light along illumination beam paths having corresponding illumination axes along which the illumination light penetrates into the microscope objective through illumination light entry sites located within a predetermined illumination light entry area of the objective; the method comprising: using the widefield microscope illumination system for a localization microscope; utilizing an illumination beam cross section at the illumination light entry sites that is smaller than the overall predetermined illumination light entry area of the objective; and repeated, automatic, parallel adjustment of the illumination axis relative to the optical objective axis at time intervals, such that a lateral offset of the illumination axis relative to the objective axis is automatically adjusted, so that the illumination light entry site is adjusted within the predetermined illumination light entry area at time intervals such that the objective is protected from damage by illumination light. 10. The illumination method according to claim 9 , wherein a parallel orientation of the illumination axes relative to the objective axis, and by maintenance of that parallelism upon automatic adjustment of the lateral offset of the illumination axis relative to the objective axis. 11. The illumination method according to claim 9 , wherein a random selection of the respective illumination light entry sites of the illumination light within the predefined illumination light entry area, and by maintenance of those respective illumination light entry sites over the respective time intervals until the respective next illumination light entry site within the predefined illumination light entry sites is randomly selected. 12. The illumination method according to claim 9 , wherein selection of the respective illumination light entry sites of the illumination light within the predefined illumination light entry area according to a predefined pattern, and by maintenance of those respective illumination light entry sites over the respective time intervals until the respective next illumination light entry site is selected within the predefined illumination light entry sites according to the predefined pattern. 13. The illumination method according to claim 9 , wherein a measurement of the optical transmittance of the objective for the respective illumination light entry sites, and adjustment of the time intervals in accordance with a change over time in optical transmittance for the respective illumination light entry site.
Fluorescence microscopy (fluorescence microscopes per se G02B21/0076 and G02B21/16) · CPC title
adapted for ultraviolet illumination {; Fluorescence microscopes (G02B21/0076 takes precedence)} · CPC title
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providing an output produced by processing a plurality of individual source images, e.g. image tiling, montage, composite images, depth sectioning, image comparison · CPC title
affording both dark- and bright-field illumination · CPC title
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