Optical system for a flow cytometer with an interrogation zone

• US 8,432,541 B2
• Filed: 11/04/2010
• Issued: 04/30/2013
• Est. Priority Date: 12/17/2007
• Status: Active Grant

• Current Assignee: Accuri Cytometers, Inc. (Becton, Dickinson & Co)
• Original Assignee: Accuri Cytometers, Inc. (Becton, Dickinson & Co)
• Inventors: Rich, Collin A.
• Primary Examiner(s): PHAM, HOA Q
• Application Number:
  US12/939,836
• Publication Number:
  US 20110058163A1
• Time in Patent Office: 908 Days
• Field of Search: 356/244, 356/246, 356/73, 356432-440, 356335-343, 356/39
• US Class Current: 356/246
• CPC Class Codes: G01N 15/1434 Optical arrangements
• CPC Class Codes: G01N 15/1459 the analysis being performed on a sample stream
• CPC Class Codes: G02B 27/141 using dichroic mirrors
• CPC Class Codes: G02B 27/145 having sequential partially reflecting surfaces

Abstract

The optical system of the preferred embodiments includes a first light source that creates a first beam of a first wavelength, a first collimating element that collimates the first beam, a second light source 102 that creates a second beam of a second wavelength, a second collimating element that collimates the second beam, a beam combining element that combines the collimated beams, and a focusing element that focuses the combined collimated beam to a single point.

Claims

1. An optical system for a flow cytometer with an interrogation zone, the system comprising:

a first optical stage including;

a first light source that creates a first beam of a first wavelength;

a first collimating element that collimates the first beam from the first light source;

a second light source that creates a second beam of a second wavelength, which is different than the first wavelength;

a second collimating element that collimates the second beam from the second light source;

a first beam combining element that combines the collimated beams of the first and second collimating elements to form a combined collimated beam that is multichromatic; and

a second optical stage including;

a third light source that creates a third beam of a third wavelength, which is different than the first and second wavelengths;

a third collimating element that collimates the third beam from the third light source; and

a second beam combining element that combines the collimated beam of the third collimating element and the combined collimated beam to form an augmented combined beam;

a bracket including an adjustable mount for the first light source and at least one of the second and third light sources, wherein the bracket allows for alignment of at least one of the second and third light sources relative to the first light source, and wherein the adjustable mount is adjustable along two axes; and

a focusing element that focuses the augmented combined beam to a single point.

2. The optical system of claim 1, wherein the first light source is a blue laser and the second light source is a violet laser or a red laser.

3. The optical system of claim 2, wherein at least one of the light sources is produced by a laser diode.

4. The optical system of claim 1, wherein the focusing element is located on a flow cell of the flow cytometer.

5. The optical system of claim 4, wherein the augmented combined beam is a collimated beam, and wherein the focusing element is configured to focus light from the augmented combined beam to a single point within the flow cell.

6. The optical system of claim 5, wherein at least one of the first and second beam combining elements is a beam splitter.

7. The optical system of claim 5, wherein the focusing element is configured to focuses a portion of a collimated beam on the single point when the collimated beam is misaligned with the focusing element.

8. The optical system of claim 7, further including an adjustable vertical lens positioned between the second beam combining element and the flow cell, wherein the adjustable vertical lens modifies a position of the augmented combined beam.

9. The optical system of claim 7, further including a changeable optical filter configured to absorb spurious emissions.

10. The optical system of claim 4, further including a beam shaping element that redistributes the phase of the augmented combined beam before the focusing element focuses the augmented combined beam.

11. The optical system of claim 1, further comprising a flow cell that defines the interrogation zone for the flow cytometer, wherein the focusing element is located on the flow cell.

12. The optical system of claim 11, wherein the augmented combined beam is a collimated beam, and wherein the focusing element is configured to focus light from the augmented combined beam to a single point within the flow cell.

13. The optical system of claim 12 wherein the focusing element is configured to focus a portion of a collimated beam on the single point when the collimated beam is misaligned with the focusing element.

14. The optical system of claim 13, further including an adjustable vertical lens positioned between the second beam combining element and the flow cell, wherein the adjustable vertical lens modifies a position of the augmented combined beam.

15. The optical system of claim 13, further including a changeable optical filter configured to absorb spurious emissions.

16. The optical system of claim 11, further including a beam shaping element that redistributes the phase of the augmented combined beam before the focusing element focuses the augmented combined beam.

17. The optical system of claim 1 wherein the first collimating element is mounted to the first light source, and wherein the second collimating element is mounted to the second light source.

18. The optical system of claim 1 further comprising a flow cell that defines the interrogation zone for the flow cytometer, wherein the focusing element is located on the flow cell.