Laser scanning type fluorescent microscope
A laser scan type fluorescence microscope includes a laser light source section, an objective optical system for condensing excitation light from the laser light source section on a sample, a scanning device to scan a surface of the sample with the excitation light from the laser light source section, a pupil projection lens arranged between the scanning device and the objective optical system, a detection optical system for detecting fluorescence that emanates from the sample and passes the objective optical system and the pupil projection lens. The objective optical system has an objective lens and an image forming lens for forming an intermediate image of the sample, and a back focal position of the objective lens is made conjugate with a position near the scanning device by the image forming lens and the pupil projection lens, wherein the following condition is satisfied: 0.15≦D/L≦0.5, where D is a parfocal distance of the objective lens, and L is a distance from the sample surface to the position conjugate with the back focal position of the objective lens and located near the scanning device.
1. A laser scan type fluorescence microscope comprising:
laser light source section;
an objective optical system constructed and arranged to condense excitation light from the laser light source section on a sample;
a scanning device constructed and arranged to scan a surface of the sample with the excitation light from the laser light source section;
a pupil projection lens arranged between the scanning device and the objective optical system; and
a detection optical system for detecting fluorescence that emanates from the sample and passes the objective optical system and the pupil projection lens,
wherein the objective optical system comprises an objective lens and an image forming lens for forming an intermediate image of the sample, wherein a back focal position of the objective lens is made conjugate with a position near the scanning device by the image forming lens and the pupil projection lens, and
wherein the following condition is satisfied:
0.15 ≦D/L≦ 0.5
where D is a parfocal distance of the objective lens, and L is a distance from the surface of the sample to the position conjugate with the back focal position of the objective lens and located near the scanning device.
2. The laser scan type fluorescence microscope according to claim 1 , further comprising an optical transmission member which leads the excitation light from the laser light source section to the scanning device.
3. The laser scan type fluorescence microscope according to claim 1 , further comprising:
a first multi-mode fiber which leads the excitation light from the laser light source section to the scanning device;
a second multi-mode fiber which leads the fluorescence from the sample to the detection optical system;
a first lens by which entry of the excitation light to the first multi-mode fiber is carried out; and
a second lens by which entry of the fluorescence to the second multi-mode fiber is carried out,
wherein the following conditions are satisfied:
2 ≦Φem/Φex≦ 12
0.61×(λ ex/NAex )<Φ ex
0.61×(λ em/NAem )<Φ em
where Φex is a diameter of a core of the first multi-mode fiber, Φem is a diameter of a core of the second multi-mode fiber, NAex is a numerical aperture where entry of the excitation light to the first multi-mode fiber by the first lens is carried out, λex is a wavelength of the excitation light, NAem is a numerical aperture where entry of the fluorescence to the second multi-mode fiber by the second lens is carried out, and λem is a wavelength of the fluorescence.
4. The laser scan type fluorescence microscope according to claim 1 , further comprising an optical transmission member which leads the fluorescence emanating from the sample and passing the pupil projection lens to the detection optical system.
5. The laser scan type fluorescence microscope according to claim 1 , further comprising a light conducting optical system that leads the fluorescence from the sample to the detection optical system and leads the excitation light from the laser light source section to the scanning device.
6. The laser scan type fluorescence microscope according to claim 1 , further comprising a first optical transmission member which leads the excitation light from the laser light source section to the scanning device, and a second optical transmission member which leads the fluorescence from the sample to the detection optical system.
7. The laser scan type fluorescence microscope according to claim 1 , wherein the detection optical system is arranged in a main body of the microscope.
8. The laser scan type fluorescence microscope according to claim 1 , further comprising:
a first multi-mode fiber which leads the excitation light from the laser light source section to the scanning device;
a second multi-mode fiber which leads the fluorescence from the sample to the detection optical system;
a first lens by which entry of the excitation light to the first multi-mode fiber is carried out; and
a second lens by which entry of the fluorescence to the second multi-mode fiber is carried out,
wherein the following conditions are satisfied:
4 ≦Φem/Φex≦ 10
0.61×(λ ex/NAex )<Φ ex
0.61×(λ em/NAem )<Φ em
where Φex is a diameter of a core of the first multi-mode fiber, Φem is a diameter of a core of the second multi-mode fiber, NAex is a numerical aperture where entry of the excitation light to the first multi-mode fiber by the first lens is carried out, λex is a wavelength of the excitation light, NAem is a numerical aperture where entry of the fluorescence to the second multi-mode fiber by the second lens is carried out, and λem is a wavelength of the fluorescence.
9. A laser scan type fluorescence microscope comprising:
a laser light source section;
an objective optical system constructed and arranged to condense excitation light from the laser light source section is condensed on a sample;
a scanning device constructed and arranged to scan a surface of the sample with the excitation light from the laser light source section;
a pupil projection lens arranged between the scanning device and the objective optical system; and
a detection optical system for detecting fluorescence that emanates from the sample and passes the objective optical system and the pupil projection lens,
wherein the objective optical system comprises an objective lens and an image forming lens for forming an intermediate image of the sample,
wherein a back focal position of the objective lens is made conjugate with a position near the scanning device by the image forming lens and the pupil projection lens,
wherein the following condition is satisfied:
0.15 ≦D/L≦ 0.5
where D is a parfocal distance of the objective lens, and L is a distance from the surface of the sample to the position conjugate with the back focal position of the objective lens and located near the scanning device,
wherein the pupil projection lens comprises a plurality of lens components, and is configured so that, of lens surfaces thereof, a lens surface arranged nearest the scanning device is concave toward a scanning device side and a lens surface arranged nearest the intermediate image is concave toward an intermediate image side, and
wherein the following condition is satisfied:
0.2 ≦Fe/D 3≦0.5
where D 3 is a distance from a position conjugate with a pupil position of the objective lens and located near the scanning device to a position of the intermediate image formed by the image forming lens, and Fe is a focal length of the pupil projection lens.
10. A laser scan type fluorescence microscope comprising:
a laser light source section;
an objective optical system constructed and arranged to condense excitation light from the laser light source section on a sample;
a scanning device for scanning a surface of the sample with the excitation light from the laser light source section;
a pupil projection lens arranged between the scanning device and the objective optical system; and
a detection optical system for detecting fluorescence that emanates from the sample and passes the objective optical system and the pupil projection lens,
wherein the objective optical system comprises an objective lens and an image forming lens for forming an intermediate image of the sample,
wherein a back focal position of the objective lens is made conjugate with a position near the scanning device by the image forming lens and the pupil projection lens,
wherein the following condition is satisfied:
0.15 ≦D/L≦ 0.5
where D is a parfocal distance of the objective lens, and L is a distance from the surface of the sample to the position conjugate with the back focal position of the objective lens and located near the scanning means, and
wherein the laser scanning confocal fluorescence microscope is composed of a plurality of lens groups, comprises at least one cemented lens having a positive lens element and a negative lens element, and satisfies the following conditions:
0.4 ≦FTL/D 1≦1
80<νp
where νp is Abbe's number of the positive lens element in the cemented lens, FTL is a focal length of the image forming lens, and D 1 is a distance from an objective lens shoulder on a main body of the microscope to a position of the intermediate image.
11. A laser scan type fluorescence microscope comprising:
a laser light source section;
an objective optical system constructed and arranged to condense excitation light from the laser light source section on a sample;
a scanning device constructed and arranged to scan a surface of the sample with the excitation light from the laser light source section;
a pupil projection lens arranged between the scanning device and the objective optical system; and
a detection optical system for detecting fluorescence that emanates from the sample and passes the objective optical system and the pupil projection lens,
wherein the objective optical system comprises an objective lens and an image forming lens for forming an intermediate image of the sample,
wherein a back focal position of the objective lens is made conjugate with a position near the scanning device by the image forming lens and the pupil projection lens,
wherein the following condition is satisfied:
0.15 ≦D/L≦ 0.5
where D is a parfocal distance of the objective lens, and L is a distance from the surface of the sample to the position conjugate with the back focal position of the objective lens and located near the scanning device, and
wherein the image forming lens comprises two lens groups that are a front group arranged on an intermediate image side and a rear group arranged on an objective lens side, the front group of the image forming lens has at least one negative lens element, and the following conditions are satisfied:
0.4 ≦D 2/ FTL≦ 1
0.7 ≦FTL 1/ FTL≦ 1.5
where FTL is a focal length of the image forming lens, FTL 1 is a focal length of the rear group of the image forming lens, and D 2 is an interval between the front group of the image forming lens and the rear group of the image forming lens.
12. The laser scan type fluorescence microscope according to any one of claims 9 , 10 and 11 , wherein the objective lens is a submerged type objective lens.
13. The laser scan type fluorescence microscope according to any one of claims 9 , 10 and 11 , wherein the laser light source section includes a semiconductor laser.