Light microscope with inner focusing objective and microscopy method for examining a plurality of microscopic objects

Patent metadata

Field	Value
Publication number	US-10422983-B2
Application number	US-201415038755-A
Country	US
Kind code	B2
Filing date	Oct 15, 2014
Priority date	Nov 27, 2013
Publication date	Sep 24, 2019
Grant date	Sep 24, 2019

Abstract

The invention relates to a light microscope for examining microscopic objects with high throughput. The microscope comprises a light source for illuminating a measuring zone, a sample vessel, in which the microscopic objects can be successively moved into the measuring zone, and a detection device for measuring detection light, which originates from a microscopic object located in the measuring zone. According to the invention, the microscope is characterized in that the imaging means comprise a detection lens having a stationary front optics and movable focusing optics, wherein the focusing optics is arranged behind the front optics and in front of an intermediate image plane, and can be adjusted for the height adjustment of a detection plane. The invention further relates to a corresponding microscopy method.

First claim

The invention claimed is:

1. A light microscope for examining a plurality of microscopic objects, comprising:
a light source to illuminate a measurement region,
a specimen vessel, in which the microscopic objects can be moved one after the other into the measurement region, the specimen vessel including a measurement tube,
imaging means and a detection unit to measure detection light coming from a microscopic object located in the measurement region,
wherein
the imaging means comprise a first detection objective with a stationary front optical system and a movable focusing optical system which is arranged behind the front optical system and in front of an intermediate image plane and can be adjusted for height adjustment of a detection plane,
electronic control means are provided and adapted to adjust, between two specimen image recordings, the detection plane by means of the focusing optical system in a direction which has a direction component in a movement direction of the microscopic objects, wherein
a plurality of specimen images are recorded one after the other,
the microscopic objects are moved at least between recordings of different specimen images, and
the recorded specimen images are put together to form a three-dimensional specimen image.

2. The light microscope according to claim 1 ,
wherein
all optical boundary areas from the specimen vessel to the front optical system are stationary during successive measurements of different microscopic objects and different detection planes.

3. The light microscope according to claim 1 ,
wherein
the focusing optical system has at least one laterally displaceable component which causes different refractive powers in dependence upon its lateral displacement.

4. The light microscope according to claim 1 ,
wherein
the focusing optical system has an optical component, a shape of which can be changed for a focus adjustment.

5. The light microscope according to claim 1 ,
wherein
conveying means are provided to convey the microscopic objects through the measurement tube.

6. The light microscope according to claim 1 ,
wherein
an illumination objective is provided to guide illuminating light into the measurement region and is arranged so that its optical axis is perpendicular to an optical axis of the first detection objective.

7. The light microscope according to claim 1 ,
wherein
the first detection objective is arranged so that its optical axis is at an angle differing from 90° relative to a longitudinal axis of the measurement tube.

8. The light microscope according to claim 1 ,
wherein
a second detection objective is provided and arranged so that two different detection planes can be simultaneously imaged with the first and second detection objectives.

9. A microscopy method for examining a plurality of microscopic objects, comprising:
illuminating a measurement region in a specimen vessel with a light source,
wherein the specimen vessel includes a measurement tube in which the microscopic objects can be moved one after the other into the measurement region,
measuring detection light coming from a microscopic object located in the measurement region with an imaging means and a detection unit; wherein the imaging means includes a detection objective with a stationary front optical system and a movable focusing optical system which is arranged behind the front optical system and in front of an intermediate image plane and can be adjusted for height adjustment of a detection plane,
providing and adapting an electronic control means to adjust, between two specimen image recordings, the detection plane by means of the focusing optical system in a direction which has a direction component in a movement direction of the microscopic objects, wherein
a plurality of specimen images are recorded one after the other,
the microscopic objects are moved at least between recordings of different specimen images, and
the recorded specimen images are put together to form a three-dimensional specimen image.

10. The microscopy method according to claim 9 , further comprising:
arranging the detection objective so that its optical axis is at an angle differing from 90° relative to a longitudinal axis of the measurement tube.

11. The microscopy method according to claim 10 , further comprising:
providing an illumination objective to guide illuminating light into the measurement region, wherein the illumination objective is arranged so that its optical axis is perpendicular to an optical axis of the detection objective.

12. The light microscope according to claim 5 ,
wherein
a container for receiving an immersion liquid is provided and arranged so that the immersion liquid completely surrounds a shell surface of the measurement tube at least in the region of the detection plane and that the front optical system is in contact with the immersion liquid in a measurement operation.

13. The light microscope according to claim 1 ,
wherein
the specimen vessel is open at the top, and
the front optical system is immersed in a specimen medium, located in the specimen vessel, in which specimen medium the microscopic objects are located.

Assignees

• Zeiss Carl Microscopy Gmbh
• Max Planck Gesellschaft

Inventors

• Lippert Helmut
• Siebenmorgen Jörg
• Huisken Jan
• Fahrbach Florian

Classifications

• G02B21/16

  adapted for ultraviolet illumination {; Fluorescence microscopes (G02B21/0076 takes precedence)} · CPC title

• G02B21/02 Primary

  Objectives · CPC title

• G02B21/34

  Microscope slides, e.g. mounting specimens on microscope slides · CPC title

• G02B21/0016

  Technical microscopes, e.g. for inspection or measuring in industrial production processes · CPC title

• G02B21/0004 Primary

  specially adapted for specific applications · CPC title