High resolution microscope and image divider assembly

Patent metadata

Field	Value
Publication number	US-9372333-B2
Application number	US-201013518108-A
Country	US
Kind code	B2
Filing date	Dec 14, 2010
Priority date	Dec 22, 2009
Publication date	Jun 21, 2016
Grant date	Jun 21, 2016

Abstract

The invention relates to a microscope having an illumination beam path with wide field illumination of a sample and a first detection beam path having a spatially resolved surface receiver, which is reached by a first part of the detection light coming from the sample via the first detection beam path, or an image divider assembly for a microscope. In order to lengthen the optical path length, at least a second part of the detection light coming from the sample is masked out of the detection beam path and, via deflection means belonging to the detection beam path, is led into a second detection beam path and, preferably via further deflection means, is deflected back in the direction of the detection in such a way that detection light is applied to at least two partial regions beside one another on the surface receiver. At least the second part of the detection light runs in an optical element having an optical density that is increased as compared with the first detection beam path, in order to lengthen the optical path length, and the optical element is designed to be displaceable at an angle, preferably perpendicular, to the optical axis of the first detection beam path in order to adjust the optical path length, and has flat surfaces, at least on the light entry and light exit side thereof; a prism is provided, preferably a glass prism, preferably at least in the second detection beam path after a first beam deflection, for deflection in a direction parallel to the first detection beam path, in order to increase the path length and for reverse deflection.

First claim

What is claimed is:

1. A high resolution microscope having an illumination beam path with wide-field illumination of a sample marked with marking molecules which can be activated or switched by a signal such that only in the activated or switched state can they be excited to emit fluorescent radiation, comprising, a source of radiation on said sample thereby activating and producing reflected fluorescent detection light, said signal being introduced to the sample in such a way that only a subset of the marker molecules present in the sample are activated, with sub-regions existing in the sample in which activated marker molecules have a minimum distance from their nearest neighboring activated marker molecules greater than or equal to a distance that represents a predetermined optical resolution, wherein the geometric locations of the marker molecules emitting the fluorescent radiation are determined with a spatial resolution enhanced beyond the predetermined optical resolution; a first detection-beam path of said detection light, a spatially resolved planar detector located within said first detection-beam path, said planar detector having a detection plane, a first part of detection light coming from said sample reaches said detection plane via said first detection-beam path or from an image splitter arrangement within said microscope, at least a second part of said detection light coming from said sample being masked out of the detection-beam path in order to lengthen the optical path length, deflection means associated with said detection-beam path, for guiding at least a second detection-beam path, a further deflection means for deflecting said second detection beam path of said detection light back in the direction of detection in such a way that detection light is caused to be incident on at least two distinct partial areas of said detection plane wherein at least the second part of the detection light runs at least in part to an optical element having a refractive index that is increased in comparison to the first detection-beam path in order to lengthen the optical path length and reaches said detection plane in a different area of said detection plane than said first part, and in that the optical element is designed to be movable at an angle perpendicular to the optical axis of the first detection beam paths in order to adjust the length of the optical path, and in that it includes flat surfaces at least on its light-entry and light-exit sides.

2. The microscope according to claim 1 , wherein a prism is provided at least in the second detection beam path after a first beam deflection for deflection in a direction parallel to the first detection-beam path in order to lengthen the path length and for reverse deflection.

3. The microscope according to claim 2 , wherein the parallel part of the second detection beam path passes through the prism.

4. The microscope according to claim 2 , wherein the prism is designed to be moved perpendicularly to the optical axis for adjusting the optical path length.

5. The microscope according to claim 1 , further comprising a telecentric beam path from the sample to the detector.

6. The microscope according to claim 1 , wherein the diversion of at least the second detection beam path occurs telecentrically in the direction of the detector plane or is located in a telecentric portion of the detection beam path.

7. The microscope according to claim 2 , wherein said prism is a glass prism.

8. A high resolution microscope having an illumination beam path with wide-field illumination of a sample marked with marking molecules which can be activated or switched by a signal such that only in the activated or switched state can they be excited to emit fluorescent radiation, comprising, a source of radiation on said sample thereby activating and producing reflected fluorescent detection light, said signal being to the sample in such a way that only a subset of the marker molecules present in the sample are activated, with sub-regions existing in the sample in which activated marker molecules have a minimum distance from their nearest neighboring activated marker molecules greater than or equal to a distance that represents a predetermined optical resolution, wherein the geometric locations of the marker molecules emitting the fluorescent radiation are determined with a spatial resolution enhanced beyond the predetermined optical resolution; a first detection beam path of said detection light that includes a spatially resolved planar detector having a detection plane, a first part of detection light coming from said sample reaching said detection plane via said first detection beam path or from an image splitter wherein at least a second part of the detection light coming from the sample is diverted out of the detection beam path in order to lengthen the optical path length and, via deflection means associated with the detection-beam path, is guided in at least a second detection beam path and, via further deflection means is deflected back in the direction of the detection in such a way that detection light is caused to be incident on at least two distinct partial areas on the detection plane so that said second part of said detection light reaches said detection plane in a different area of said detection plane than said first part, and wherein at least one part of the deflection means is designed for being movable at an angle to the optical axis of the first detection beam path for adjustment of the optical path length.

9. The microscope according to claim 8 , wherein said angle is 90°.

10. A high resolution microscope having an illumination beam path with wide-field illumination of a sample marked with marking molecules which can be activated or switched by a signal such that only in the activated or switched state can they be excited to emit fluorescent radiation, comprising, a source of radiation on said sample thereby activating and producing reflected fluorescent detection light, said signal being introduced to the sample in such a way that only a subset of the marker molecules present in the sample are activated, with sub-regions existing in the sample in which activated marker molecules have a minimum distance from their nearest neighboring activated marker molecules greater than or equal to a distance that represents a predetermined optical resolution, wherein the geometric locations of the marker molecules emitting the fluorescent radiation are determined with a spatial resolution enhanced beyond the predetermined optical resolution; a first detection beam path of said detection light that includes a spatially resolved planar detector having a detection plane, a first part of detection light coming from said sample reaching said detection plane via said first detection beam path, or from image splitter, wherein at least a second part of the detection light coming from the sample is diverted out of the detection beam path in order to lengthen the optical path length and, via deflection means associated with the detection-beam path, it is guided in at least a second detection beam path and, via further deflection means, is deflected back in the direction of the detection in such a way that detection light is caused to be incident on at least two distinct partial areas on said detection plane, wherein a splitting takes place into four detection beam paths that impinge upon one or more detectors at an offset to one another via partially transparent mirrors and deflection elements.

11. The microscope according to claim 10 , wherein three partially transparent mirrors and three deflection elements are provided for splitting, and the partially transparent mirrors preferably exhibit splitting ra

Assignees

• Kalkbrenner Thomas
• Goelles Michael
• Zeiss Carl Microscopy Gmbh

Inventors

• Kalkbrenner Thomas
• Goelles Michael

Classifications

• G02B21/361 Primary

  Optical details, e.g. image relay to the camera or image sensor (G02B21/364 takes precedence; illumination details G02B21/06 and subgroups) · CPC title

• G01N21/6458

  Fluorescence microscopy (fluorescence microscopes per se G02B21/0076 and G02B21/16) · 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

• G02B21/0072

  details concerning resolution or correction, including general design of CSOM objectives · CPC title

• G02B21/0076

  arrangements using fluorescence or luminescence · CPC title