Biological observation apparatus

Patent metadata

Field	Value
Publication number	US-9810895-B2
Application number	US-78675010-A
Country	US
Kind code	B2
Filing date	May 25, 2010
Priority date	May 29, 2009
Publication date	Nov 7, 2017
Grant date	Nov 7, 2017

Abstract

A biological observation apparatus includes a light source that radiates illumination light onto an observation region that includes a biological specimen; a CCD that acquires a macro image of the observation region; a light source that radiates excitation light onto the biological specimen; a micro-image acquisition unit that acquires a micro image of the biological specimen; an identification-information storing unit that stores identification information of the biological specimen; a biological-specimen specifying unit that extracts identification information of the biological specimen by performing image processing on the macro image, and specifies a biological specimen for which the extracted identification information corresponds to the identification information stored in the identification-information storing unit; and a pan controller that moves a capturing range of the micro-image acquisition unit such that the biological specimen is included in the viewing range of the micro image.

First claim

What is claimed is:

1. A method for creating an image of a moving live-cell specimen using an observation apparatus comprising a microscope system and an information storage unit, wherein the microscope system comprises a stage on which the live-cell specimen is mounted and an objective lens that collects observation light from the live-cell specimen while focusing illumination light thereon, the method comprising:
acquiring, with the microscope system, a micro image of the live-cell specimen;
acquiring, with the microscope system, a three-dimensional macro image of an observation region that includes the live-cell specimen, by varying a relative position of the objective lens and the live-cell specimen in an optical axis direction, wherein a viewing range of the microscope system when acquiring the macro image is larger than a viewing range of the microscope system when acquiring the micro image;
extracting identification information of the live-cell specimen included in the macro image by performing image processing on the macro image;
storing, in the information storage unit, identification information of the live-cell specimen which moves and which is observed as a target;
specifying, as a specified live-cell specimen, the live-cell specimen to which the extracted identification information corresponds in the identification information stored in the information storage unit;
calculating an amount of movement of the specified live-cell specimen included in the macro image; and
adjusting repeatedly, according to a movement of the live-cell specimen, a position of the viewing range of the microscope system in a direction that intersects an optical axis, based on the calculated amount of movement of the specified live-cell specimen, such that the specified live-cell specimen is included in the viewing range of the microscope system.

2. The method according to claim 1 , wherein the observation apparatus further comprises a scanner and a light source, the method further comprising:
scanning, with the scanner, irradiation light emitted from the light source on the live-cell specimen;
detecting, with the microscope system, observation light from a scanning range of the irradiation light scanned in the observation region by the scanner, in the acquisition of the macro image;
detecting, with the microscope system, observation light from another scanning range of the irradiation light scanned in the observation region by the scanner, in the acquisition of the micro image; and
controlling a swing angle range of the scanner such that a scanning amplitude of the irradiation light is smaller when acquiring the micro image than when acquiring the macro image.

3. The method according to claim 2 , further comprising:
adjusting a swing range position of the scanner such that the specified live-cell specimen is included in the viewing range of the microscope system.

4. The method according to claim 2 , further comprising:
radiating, with the objective lens, the irradiation light scanned by the scanner onto the live-cell specimen; and
moving the stage, and adjusting relative positions of the objective lens and the stage in the direction that intersects the optical axis, such that the specified live-cell specimen is included in the viewing range of the microscope system.

5. The method according to claim 1 , wherein the observation apparatus further comprises a scanner and a light source, the method further comprising:
scanning, with the scanner, irradiation light emitted from the light source on the live-cell specimen;
capturing, with the microscope system, observation light from an area in the observation region irradiated with the irradiation light emitted from the light source, in the acquisition of the macro image;
detecting, with the microscope system, observation light from a scanning range of the irradiation light scanned in the observation region by the scanner, in the acquisition of the micro image; and
controlling a swing angle range of the scanner such that the viewing range of the microscope system for the micro image is smaller than the viewing range thereof for the macro image.

6. The method according to claim 5 , further comprising adjusting a swing range position of the scanner such that the specified live-cell specimen is included in the viewing range of the microscope system.

7. The method according to claim 5 , further comprising:
radiating, with objective lens, the irradiation light scanned by the scanner onto the live-cell specimen, and
moving the stage, and adjusts relative positions of the objective lens and the stage in the direction that intersects the optical axis, such that the specified live-cell specimen is included in the viewing range of the microscope system.

8. The method according to claim 1 , wherein the observation apparatus further comprises: (i) a plurality of objective lenses of different magnifications, and (ii) a revolver that holds the plurality of objective lenses and that disposes the plurality of objective lenses in an optical path of irradiation light in an exchangeable manner, the method further comprising:
collecting, with the plurality of objective lenses, observation light from the live-cell specimen and an observation region that includes the live-cell specimen;
capturing, with the microscope system, observation light coming from the observation region and collected by an objective lens from among the plurality of objective lenses having a low magnification, in the acquisition of the macro image;
capturing, with the microscope system, observation light coming from the live-cell specimen and collected by an objective lens from among the plurality of objective lenses having a high magnification, in the acquisition of the micro image; and
moving the stage, and adjusting relative positions of the objective lens having the high magnification and the stage in the direction that intersects the optical axis, such that the specified live-cell specimen is included in the viewing range of the microscope system.

9. The method according to claim 8 , further comprising extracting the identification information of the live-cell specimen included in the macro image by using magnification information of the objective lens that acquires the micro image.

10. The method according to claim 1 , further comprising adjusting relative positions of the objective lens and the stage in the direction that intersects the optical axis such that the specified live-cell specimen is included in the viewing range of the microscope system.

11. The method according to claim 10 , further comprising:
acquiring a plurality of the macro images having adjacent observation regions; and
assembling the adjacent macro images.

12. The method according to claim 1 , wherein:
the micro image of the live-cell specimen is acquired based on fluorescence excited by illumination light emitted from a first light source.

13. The method according to claim 1 , further comprising rewriting the identification information of the live-cell specimen stored in the information storage unit with updated identification information of the live-cell specimen based on a change in the identification information of the live-cell specimen extracted from the macro image.

14. The method according to claim 1 , further comprising:
storing identification information of live-cell specimens newly formed by cell division in the identification information storing unit; and
assigning mutually linked identifiers to each of the new live-cell specimens formed by the cell division from a same live-cell specimen in response to the cell division of the live-

Assignees

• Kimura Hiroyuki
• Olympus Corp

Inventors

• Kimura Hiroyuki

Classifications

• G02B21/0076

  arrangements using fluorescence or luminescence · CPC title

• G02B21/367 Primary

  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

• G02B21/008

  Details of detection or image processing, including general computer control · CPC title

• G02B21/0072

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

• G02B21/002

  Scanning microscopes (scanning near field optical microscopes G01Q60/18) · CPC title