APPARATUS AND METHOD OF ACQUIRING IMAGES OF A SAMPLE OF BIOLOGICAL ORIGIN

• US 20100219353A1
• Filed: 12/26/2006
• Published: 09/02/2010
• Est. Priority Date: 12/27/2005
• Status: Abandoned Application

• Current Assignee: Olympus Corporation
• Original Assignee: Olympus Corporation
• Inventors: Suzuki, Hirobumi, Fukuoka, Morinao, Akiyoshi, Ryutaro
• Application Number:
  US12/159,357
• Publication Number:
  US 20100219353A1
• Time in Patent Office: Days
• US Class Current: 250/459.100
• CPC Class Codes: G01N 21/6458 Fluorescence microscopy fluorescence microscopes per se G02B21/0076 and G02B21/16
• CPC Class Codes: G02B 21/0088 Inverse microscopes

Abstract

A novel apparatus and a novel method of imaging a luminescence phenomenon of a sample of biological origin using an optical image formation device are provided. In the inventive method and apparatus, an illumination image acquired by illuminating the sample and a luminescence image acquired with the light emitted by a luminescence phenomenon of a cell in the sample without illuminating it are superposed to generate a superposition image. In the superposition image, an analysis region is determined. Thereby, even when the light detected in a luminescence observation is feeble, a luminescent cell and/or a luminescent site in a cell in a sample can be specified.

Claims

1. An apparatus acquiring an image of a sample of biological origin with an optical image formation device, comprising an illuminating portion which illuminates the sample;

an illumination image acquiring portion which acquires an illumination image of the sample, a luminescence image acquiring portion which acquires a luminescence image of a cell in the sample;

an image processing portion which superposes the illumination image and the luminescence image to generate a superposition image, and determines an analysis region in the superposition image.

2. An apparatus of claim 1, characterized in that the optical image formation device is an optical microscope;

the illumination image is a transmitted light microscopic image obtained in a transmitted light observation with illumination light of the illuminating portion under the optical microscope and the luminescence image is a luminescence microscopic image obtained by observing light emitted by a luminescence phenomenon in the cell under the optical microscope;

wherein the illumination image acquiring portion and the luminescence image acquiring portion comprise a common microscopic image capturing device which captures the transmitted light microscopic image and the luminescence microscopic image.

3. An apparatus of claim 2, characterized in that the microscopic image capturing device has a light receiving surface and the optical microscope includes an objective and a lens assembly which form the images of the sample on the light receiving surface of the microscopic image capturing device, wherein a square value of a ratio of a numerical aperture of the objective to a magnification power of the image of the sample projected on the light receiving surface is 0.01 or above.

4. An apparatus of claim 1 characterized in that the apparatus comprises a fluorescence image acquiring portion for acquiring a fluorescence image of the cell.

5. An apparatus of claim 4, characterized in that the optical image formation device is an optical microscope;

the fluorescence image is a fluorescence microscopic image obtained in a fluorescence observation of the sample under the optical microscope and the luminescence image is a luminescence microscopic image obtained by observing light emitted by a luminescence phenomenon in the cell under the optical microscope;

wherein the fluorescence image acquiring portion and the luminescence image acquiring portion comprise a common microscopic image capturing device which captures the fluorescence microscopic image and the luminescence microscopic image.

6. An apparatus of claim 1 characterized in that the apparatus comprises a display portion which displays the superposition image.

7. An apparatus of claim 1 characterized in that the apparatus comprises a recording portion which records the superposition image.

8. An apparatus of claim 1 characterized in that the apparatus comprises a cell stimulus feeding portion which stimulates a cell.

9. An apparatus of claim 8, characterized in that the cell stimulus feeding portion is at least one selected from a group consisting of a reagent feeding portion which supplies a reagent to the cell, a temperature adjustment portion which adjusts a temperature of the sample and a gas feeding portion which supplies gas to the cell.

10. A method of acquiring an image of a sample of biological origin by means of an optical image formation device, characterized in that the method comprises the steps of:

illuminating the sample and acquiring its illumination image;

acquiring a luminescence image of light emitted by a luminescence phenomenon of a cell in the sample without illuminating the sample;

superposing the illumination image and the luminescence image to generate a superposition image; and

determining an analysis region in the superposition image.

11. A method of claim 10, characterized in that the method comprises a step of displaying the superposition image.

12. A method of claim 10, characterized in that the method comprises a step of recording the superposition image.

13. A method of claim 10, characterized in that the step of illuminating the sample and acquiring the illumination image is performed two or more times.

14. A method of claim 10, characterized in that the method comprises a step of giving a stimulus to the cell prior to the steps of acquiring the illumination image and the luminescence image.

15. A method of claim 14, characterized in that the method comprises a step of acquiring the illumination image and the luminescence image prior to the step of giving a stimulus to the cell.

16. A method of claim 14, characterized in that the stimulus given to the cell in the step of giving the stimulus to the cell is at least one of stimuli selected from the group consisting of a reagent stimulus, an electric stimulus, a stimulus by gas and a stimulus by heat.

17. A method of claim 10, characterized by further comprising steps of:

measuring a light intensity of a region in the luminescence image corresponding to the analysis region, and displaying a variation in the light intensity.

18. A method of claim 10, characterized in that the method comprises a step of acquiring a fluorescence image of the cell in the sample.

19. A method of claim 18, characterized in that the method comprises a step of displaying at least two regions among a region in the illumination image corresponding to the analysis region;

a region in the luminescence image corresponding to the analysis region; and

a region in the fluorescence images corresponding to the analysis region.

20. A method of claim 10, characterized in that the optical image formation device is an optical microscope;

the illumination image is a transmitted light microscopic image obtained in a transmitted light observation under the optical microscope and the luminescence image is a luminescence microscopic image obtained by observing light emitted by a luminescence phenomenon in the cell under the optical microscope;

wherein the transmitted light microscopic image and the luminescence microscopic image are captured with a common microscopic image capturing device.

21. A method of claim 20, characterized in that the microscopic image capturing device has a light receiving surface and the optical microscope includes an objective and a lens assembly which form the images of the sample on the light receiving surface of the microscopic image capturing device, wherein a square value of a ratio of a numerical aperture of the objective to a magnification power of the image of the sample projected on the light receiving surface is 0.01 or above.

22. An apparatus of acquiring an image of a sample of biological origin comprising an optical microscope, a microscopic image capturing device which captures a microscopic image of the sample observed with the optical microscope, and an image processing device which takes in the microscopic image as an image data and executes image processing, wherein the image processing device comprises an image superposing portion which generates a superposition image by superposing a transmitted light image obtained by capturing an image of the sample in a transmitted light observation of the sample under the optical microscope with the microscopic image capturing device and a luminescence image obtained by capturing light emitted by a luminescence phenomenon in a cell in the sample under the optical microscope with the microscopic image capturing device;

and an image region specifying portion which specifies an analysis region in the superposition image.

23. An apparatus of claim 22, characterized in that the microscopic image capturing device has a light receiving surface and the optical microscope includes an objective and a lens assembly which form the images of the sample on the light receiving surface of the microscopic image capturing device, wherein a square value of a ratio of a numerical aperture of the objective to a magnification power of the image of the sample projected on the light receiving surface is 0.01 or above.