ILLUMINATION OPTICAL SYSTEM AND MICROSCOPE

• US 20150124073A1
• Filed: 08/29/2013
• Published: 05/07/2015
• Est. Priority Date: 08/29/2012
• Status: Abandoned Application

• Current Assignee: Canon Ayutthaya Limited (Canon Inc.)
• Original Assignee: Canon Ayutthaya Limited (Canon Inc.)
• Inventors: Morishima, Hideki, Fujishima, Hironobu, Matsuura, Hiroshi
• Application Number:
  US14/397,345
• Publication Number:
  US 20150124073A1
• Time in Patent Office: Days
• US Class Current: 348/79
• CPC Class Codes: G01N 21/6458 Fluorescence microscopy fluorescence microscopes per se G02B21/0076 and G02B21/16
• CPC Class Codes: G02B 21/0092 Polarisation microscopes
• CPC Class Codes: G02B 21/06 Means for illuminating specimens
• CPC Class Codes: G02B 21/16 adapted for ultraviolet illumination ; Fluorescence microscopes G02B21/0076 takes precedence
• CPC Class Codes: G02B 21/361 Optical details, e.g. image relay to the camera or image sensor G02B21/364 takes precedence; illumination details G02B21/06 and subgroups

Abstract

The illumination optical system is configured to illuminate a sample placed on an object plane with light. The illumination optical system includes multiple light source areas which are mutually coherent and arranged separately from one another in a pupil plane of the illumination optical system. Among distances from a center of a pupil of the illumination optical system to centers of the multiple light source areas, at least one of the distances is different from the other distances.

Claims

1. An illumination optical system configured to illuminate a sample placed on an object plane with light, the illumination optical system comprising:

multiple light source areas which are mutually coherent and arranged separately from one another in a pupil plane of the illumination optical system,

wherein, among distances from a center of a pupil of the illumination optical system to centers of the multiple light source areas, at least one of the distances is different from the other distances.

2. An illumination optical system according to claim 1, wherein the sample is an autoluminescent.

3. An illumination optical system according to claim 1, wherein a luminescence mechanism of the sample, which is the autoluminescent, is fluorescence or phosphorescence.

4. A microscope comprising:

an illumination optical system configured to illuminate a sample placed on an object plane with light; and

a projection optical system configured to form an image of the sample,

wherein the illumination optical system comprising;

an optical element configured to form multiple light source areas which are mutually coherent and arranged separately from one another in a pupil plane of the illumination optical system,

wherein, among distances from a center of a pupil of the illumination optical system to centers of the multiple light source areas, at least one of the distances is different from the other distances.

5. A microscope according to claim 4, further comprising:

a first camera port and a second camera port disposed at positions each optically conjugate with the object plane,

wherein the first camera port includes an image sensor to perform image capturing of the sample, and

wherein the second camera port configured to receive multiple collimated light beams which are mutually coherent to form the mutually coherent light source areas in the pupil plane of the illumination optical system, a ratio of a size of each light source area to a radius of the pupil of the illumination optical system being smaller than 0.3.

6. A microscope according to claim 5, wherein the second camera port causes the mutually coherent collimated light beams to reach the object plane with incident angles such that the mutually coherent collimated light beams each form a beam waist and mutually overlap at the position optically conjugate with the object plane.

7. A microscope according to claim 5, further comprising an optical element configured to block an excitation light and transmit fluorescence or phosphorescence and disposed between the first camera port and a branching point of an optical path from the object plane to the second camera port and an optical path from the object plane to the first camera port.

8. A microscope according to claim 5, further comprising a movable light-blocking element configured to be switchable between a state of blocking at least one of the mutually coherent collimated light beams and a state of passing through all of them the at least one collimated light beam.

9. A microscope according to claim 8, wherein the light-blocking element has a function of blocking fluorescence or phosphorescence from a sample.

10. A microscope according to claim 8, wherein the light-blocking element includes at least one polarizer.

11. A microscope according to claim 5, further comprising a control mechanism configured to control coherence of the mutually coherent collimated light beams.

12. A microscope according to claim 10, further comprising a control mechanism configured to control polarization directions of the mutually coherent collimated light beams, the control mechanism including at least one polarizer.

13. A microscope according to claim 5, wherein the microscope is a fluorescence microscope.

14. A microscope according to claim 5, wherein the microscope is an epi-illumination microscope or a transmission microscope.

15. A microscope according to claim 6, further comprising an optical element configured to block an excitation light and transmit fluorescence or phosphorescence and disposed between the first camera port and a branching point of an optical path from the object plane to the second camera port and an optical path from the object plane to the first camera port.

16. A microscope according to claim 6, further comprising a movable light-blocking element configured to be switchable between a state of blocking at least one of the mutually coherent collimated light beams and a state of passing through all of them the at least one collimated light beam.

17. A microscope according to claim 16, wherein the light-blocking element has a function of blocking fluorescence or phosphorescence from a sample.

18. A microscope according to claim 7, further comprising a movable light-blocking element configured to be switchable between a state of blocking at least one of the mutually coherent collimated light beams and a state of passing through all of them the at least one collimated light beam.

19. A microscope according to claim 9, wherein the light-blocking element includes at least one polarizer.

20. A microscope according to claim 6, further comprising a control mechanism configured to control coherence of the mutually coherent collimated light beams.