Optical device with a high collection efficiency and cytofluorimeter making use of the same

• US 4,673,289 A
• Filed: 06/17/1985
• Issued: 06/16/1987
• Est. Priority Date: 06/20/1984
• Status: Expired due to Term

• Current Assignee: Hycel Diagnostics (Escalon Medical Corporation)
• Original Assignee: Commissariat a L'Energie Atomique (French Alternative Energies and Atomic Energy Commission)
• Inventors: Gaucher, Jean-Claude
• Primary Examiner(s): EVANS, FANNIE L
• Application Number:
  US06/745,589
• Time in Patent Office: 729 Days
• Field of Search: 250/461.1, 250/461.2, 250/573, 250/574, 250/575, 356/39, 356/72, 356/73, 356/246, 356/317, 356/318, 356/335, 356/336, 356/337, 356/338, 356/343, 356/410, 356/411, 350/416
• US Class Current: 356/72
• CPC Class Codes: G01N 15/1436 the optical arrangement forming an integrated apparatus with the sample container, e.g. a flow cell
• CPC Class Codes: G01N 15/1459 the analysis being performed on a sample stream
• CPC Class Codes: G01N 15/149 specially adapted for sorting particles, e.g. by their size or optical properties
• CPC Class Codes: G01N 2015/1019 Associating Coulter-counter and optical flow cytometer [OFC]
• CPC Class Codes: G01N 2015/1024 Counting particles by non-optical means
• CPC Class Codes: G02B 19/0028 refractive and reflective surfaces, e.g. non-imaging catadioptric systems
• CPC Class Codes: G02B 19/0047 for use with a light source G02B19/009, G02B19/0095 take precedence; details of lighting devices in general F21V; non-semiconductor lasers having optical devices external to the laser cavity H01S3/005
• CPC Class Codes: G02B 19/0095 for use with ultraviolet radiation

Abstract

Optical device with a high collection efficiency and cytofluorimeter using the same. This device permits the light excitation of a flow of material directed along an axis and able to emit light when it receives it and/or collects the light emitted by said flow. It comprises a first optical element and a spherical analysis chamber which can be penetrated by the flow, defined by the element and allowing a center of symmetry. The element has a convex spherical dioptre allowing an axis of symmetry passing through the center of the chamber and said element is positioned in such a way that the axis of the flow passes through the center of the chamber. Application to the analysis of a flow of biological cells.

Claims

1. An optical device permitting at least one of the two following operations, namely

(a) the luminous excitation of an axial flow of material to be analyzed, said flow being directed along an axis and being able to emit light when said flow receives some light and

(b) the collection of light emitted by said flow,

said device comprising a first optical element and an analysis chamber which chamber has a spherical shape, is formed within the first optical element and has a symmetry centre, said chamber being open at two diametrically opposite ends,

the first optical element having an inner concave spherical dioptre, an outer convex spherical dioptre, and an axis of symmetry passing through the symmetry centre of the chamber and

the first optical element being positioned in such a way that the axis of the material flow passes through the two ends and the centre of the chamber,

said optical device also comprising a second optical element having an inner concave dioptre, an outer convex dioptre and an axis of symmetry, said second optical element positioned in such a way that the inner dioptre of the second optical element faces the outer dioptre of the first optical element, and that the symmetry axis of the second optical element coincides with the symmetry axis of the first optical element.

2. A device according to claim 1, wherein the analysis chamber has an optically reflecting wall positioned opposite the outer dioptre of the first optical element with respect to the chamber centre.

3. A device according to claim 1, wherein the outer dioptre of the first optical element has at least a first and a second Weierstrass point and wherein said first Weierstrass point coincides with the center of the analysis chamber.

4. A device according to claim 1, wherein the two dioptres of the second optical element have a common symmetry axis, which is the same as the symmetry axis of the second optical element.

5. A device according to claim 3, wherein the second Weierstrass point of the outer dioptre of the first optical element constitutes both the centre of the first dioptre of the second optical element and a first Weierstrass point of the second dioptre of the second optical element.

6. A device according to claim 4, further comprising a collection lens positioned facing the second dioptre of the second optical element, the optical axis of which collection lens coincides with the symmetry axis of said second dioptre,

said collection lens being capable of forming a parallel light beam from the light which said collection lens collects from the second dioptre.

7. A cytofluorimeter comprising:

means for forming a flow of biological cells directed along an axis, said cells being able to emit light when they receive some light;

means for forming at least one light beam for causing luminous excitation of said cells;

an optical device for transmitting said light beam thereby permitting said cell excitation and the collection of any light emitted by the flow of cells; and

means for analyzing said light;

wherein the optical device comprises a first optical element and a spherical analysis chamber formed within said first optical element and having a symmetry centre, said chamber being open at two diametrically opposite ends,

the first optical element having an inner concave spherical dioptre, an outer convex spherical dioptre, and an axis of symmetry passing through the symmetry centre of the chamber and

the first optical element being positioned in such a way that the axis of the material flow passes thorugh the two ends and the centre of the chamber.

said optical device also comprises a second optical element having an inner concave dioptre, an outer convex dioptre and an axis of symmetry, said second optical element positioned in such a way that the inner dioptre of the second optical element faces the outer dioptre of the first optical element, and that the symmetry axis of the second optical element coincides with the symmetry axis of the first optical element.

8. A cytofluorimeter according to claim 7, wherein at least one area of the outer dioptre of the first optical element has at least one flat portion for the entry of the light beam.

9. A cytofluorimeter according to claim 7, further comprising a light reflector for reflecting part of the light diffused and nonabsorbed by the flow of cells and for forming a parallel light beam from said diffused and non-absorbed light part.

10. A cytofluorimeter according to claim 7, further comprising:

a collection lens positioned facing the second dioptre of the second optical element, the optical axis of which collection lens coincides with the symmetry axis of said second dioptre,

said collection lens being capable of forming a parallel light beam from the light which said collection lens collects from the second dioptre; and

an optical assembly for transforming the parallel light beam formed by the collection lens into a convergent light beam.

11. A cytofluorimeter according to claim 10, wherein the axis of the flow of cells is perpendicular to the axis of symmetry of the outer dioptre of the first optical element, wherein the excitation light beam is a laser beam striking the flow of cells at a point separate from the centre of the chamber, wherein the analysis chamber has an optically reflecting wall positioned opposite to the outer dioptre of the first optical element with respect to the centre of the chamber and further comprising a cylindrical lens positioned following the optical assembly and able to form tow parallel light layers from the light emerging from said assembly, at least one analysis slit for said layers and which can be displaced transversely with respect thereto and positioned following the cylindrical lens, and photodetector means positioned following the analysis slit.

12. A cytofluorimeter according to claim 10, wherein the axis of the flow fo cells is perpendicular to the axis of symmetry of the outer dioptre of the first optical element, wherein the excitation of the cells is carred out with the aid of a first laser beam and a second laser beam striking the flow of cells respectively in the centre of the analysis chamber and at a point separate from said centre and wherein the analysis chamber has an optically reflecting wall positioned opposite to the outer dioptre of the first optical element with respect to the centre of the chamber.

13. A cytofluorimeter according to claim 8, further comprising a first lens defined by a planar face and by a convex spherical dioptre, the planar face being placed against said flat portion of the first optical element, a second lens defined by a convex spherical dioptre and by a concave spherical dioptre facing the convex dioptre of the first lens and a telescope for transforming the light beam into a convergent bean with a large diameter and covering at most the convex dioptre of the second lens, wherein a first Weierstrass point of the dioptre of the first lens coincides with the centre of the analysis chamber and wherein a second Weierstrass point of this dioptre constitues both the centre of the concave dioptre of the second lens and a first Weierstrass point of the convex dioptre of said second lens.

14. A cytofluorimeter according to claim 7, wherein the light beam formation means directs said light beam into the optical device in such a way that the light beam strikes the dioptre of the first optical element of said optical device.

15. A cytofluorimeter according to claim 7, further comprising means for electrically analyzing the said cells.

16. A cytofluorimeter according to claim 7 wherein the means for forming the flow comprise a first nozzle which issues into the chamber via one of said two diametrically opposite ends, and

the cytofluorimeter further comprises:

a second nozzle which issues out of the chamber via the other of said two diametrically opposite ends and is located facing said first nozzle;

means for electrically analyzing the said cells, and

means for sorting the cells, said sorting means being positioned at the exit of said second nozzle.