Confocal incident-light scanning microscope with means for frequency conversion

Patent metadata

Field	Value
Publication number	US-9588326-B2
Application number	US-201214130966-A
Country	US
Kind code	B2
Filing date	Jul 5, 2012
Priority date	Jul 8, 2011
Publication date	Mar 7, 2017
Grant date	Mar 7, 2017

Abstract

A microscope which makes possible a spectrally-flexible excitation and detection of fluorescence in an economical manner. For this purpose, means for frequency conversion are arranged in the common beam path and a filter for excitation light is arranged in addition to the main beam splitter in the detection beam path. The frequency conversion achieves a spectral delimitation between illumination light, which is emitted by the light source, and excitation light which brings about fluorescence excitation in the specimen. Because the frequency conversion takes place in the common beam path after the main beam splitter, it is possible for both a spatial separation of illumination light, and excitation light and fluorescent light (detection light) emitted by the specimen, to be carried out in an economical manner at the main beamsplitter according to spectral bands because of the spectral difference between illumination light and excitation light.

First claim

The invention claimed is:

1. A confocal scanning microscope for fluorescence excitation by means of excitation light, comprising:
an illumination beam path;
a detection beam path;
a main beamsplitter which couples part of the illumination beam path and part of the detection beam path to form a common beam path;
an adjustable deflection unit in the common beam path;
a means for frequency conversion which is arranged in the common beam path between the main beam splitter and a part of the common beam path; and
in addition to the main beamsplitter, a filter for excitation light is arranged in the detection beam path.

2. The confocal scanning microscope according to claim 1 ;
wherein the main beamsplitter is a spectral edge filter.

3. The confocal scanning microscope according to claim 1 ;
wherein the means for frequency conversion are formed as at least one optically nonlinear medium.

4. The confocal scanning microscope according to claim 3 ;
wherein the optically nonlinear medium is arranged in a focal plane of the common beam path or at least in the area of such a focal plane.

5. The confocal scanning microscope according to claim 3 ;
wherein the at least one optically nonlinear medium is configured to convert infrared light into visible light.

6. The confocal scanning microscope according to claim 4 ;
wherein the optically nonlinear medium is arranged in the center of a 4f arrangement.

7. The confocal scanning microscope according to claim 1 ;
wherein a confocal diaphragm is arranged confocally in the detection beam path.

8. The confocal scanning microscope according to claim 7 ;
wherein the confocal diaphragm is formed by the means for frequency conversion.

9. The confocal scanning microscope according to claim 7 ,
wherein the confocal diaphragm is a pinhole diaphragm or a slit diaphragm, and is arranged confocally in the common beam path.

10. The confocal scanning microscope according to claim 1 , further comprising:
a tunable light source arranged in the illumination beam path configured to emit at least one of a plurality of different first spectral bands;
wherein the filter for the excitation light is adjustable for blocking at least one of various second spectral bands which arise from the frequency conversion from the first spectral bands.

11. The confocal scanning microscope according to claim 10 ;
wherein the filter is configured to be tilted with respect to the detection beam path for adjusting one of the second spectral bands to be blocked.

12. The confocal scanning microscope according to claim 10 ;
wherein the tunable light source is configured to emit at least one of a plurality of different infrared spectral bands.

13. The confocal scanning microscope according to claim 1 ;
wherein the illumination beam path comprises an adjustable filter configured to adjust different spectral bands of the illumination light.

14. The confocal scanning microscope according to claim 13 ;
wherein the adjustable filter is an acousto-optic tunable filter.

15. The confocal scanning microscope according to claim 1 ;
wherein the means for frequency conversion are connected to a drive for moving the means for frequency conversion out of the common beam path and into the common beam path.

16. The confocal scanning microscope according to claim 15 ;
wherein the drive which moves the means for frequency conversion out of the common beam path and into the common beam path, is configured to alternatively move one of a plurality of means for frequency conversion into the common beam path.

17. The confocal scanning microscope according to claim 1 ;
wherein the means for frequency conversion comprise at least one element of the group of elements consisting of:
periodically poled nonlinear crystal;
periodically poled nonlinear optical waveguide; and
nonlinear photonic crystal fiber.

18. The confocal scanning microscope according to claim 1 ;
wherein, in addition to the deflection unit, adjustably deflecting optical elements are arranged the common beam path, and are configured to temporally sequentially spread the beam path and to recombine the beam path.

19. The confocal scanning microscope according to claim 1 ;
wherein the main beamsplitter is:
a two-dimensional matrix of micro-optomechanical systems; or
a two-dimensional micromirror matrix; or
a mirror with at least one transmission window.

20. An operating method for a confocal scanning microscope for fluorescence excitation, comprising:
coupling illumination light, emitted by a light source in a first spectral band, along an illumination beam path via a main beamsplitter into a common beam path shared with a detection beam path;
converting the coupled illumination light within the common beam path into a different spectral band as excitation light;
guiding the converted illumination light, via a deflection unit and an objective, to a specimen;
receiving, from the specimen, light via the objective along the common beam path;
guiding the received light, via the main beamsplitter and through a filter for the excitation light, to a detector, and
optoelectronically converting the light received by the detector.

21. A non-transitory computer-readable medium which stores a computer program for controlling a confocal scanning microscope, the computer program performing the method according to claim 20 .

22. The method according to claim 20 ;
wherein the light received by the detector is optoelectronically converted by adjustment of a tunable light source to one of a plurality of first spectral bands, and adjustment of the filter for the excitation light to corresponding second spectral bands.

23. A control unit for controlling a confocal scanning microscope, where the control unit is configured to implement the method according to claim 20 .

Assignees

• Schwedt Daniel
• Wolleschensky Ralf
• Zeiss Carl Microscopy Gmbh

Inventors

• Schwedt Daniel
• Wolleschensky Ralf

Classifications

• G02F1/353

  Frequency conversion, i.e. wherein a light beam is generated with frequency components different from those of the incident light beams · CPC title

• G02F1/29

  for the control of the position or the direction of light beams, i.e. deflection · CPC title

• G02B21/0076 Primary

  arrangements using fluorescence or luminescence · CPC title

• G02B21/0032

  Optical details of illumination, e.g. light-sources, pinholes, beam splitters, slits, fibers (G02B21/0036 - G02B21/008; means for illumination of specimens in general G02B21/06) · CPC title