Prism-based flow cytometry excitation optics

• US 20040061853A1
• Filed: 09/27/2002
• Published: 04/01/2004
• Est. Priority Date: 09/27/2002
• Status: Abandoned Application

• Current Assignee: Becton, Dickinson & Co
• Original Assignee: Becton, Dickinson & Co
• Inventors: Blasenheim, Barry J.
• Application Number:
  US10/256,883
• Publication Number:
  US 20040061853A1
• Time in Patent Office: Days
• US Class Current: 356/318
• CPC Class Codes: G01N 15/1434 Optical arrangements

Abstract

A prism-based cytometry excitation optics system redirects, shapes and combines plural beams provided by light sources, so they can be focused by an objective into closely spaced spots within the channel of a cytometry flow cell. The mounted set of dispersive prisms redirect beams of different wavelengths so that beams with separated inputs emerge from the final prism, substantially overlapping in position and nearly parallel to one another. Preferred embodiments having a mounted set of four distinct isosceles triangular prisms are described with particular orientations and positions, but the specific design parameters may vary depending on the choice of beam wavelengths, spot separations in the flow cell, and choice of prism material. The prism system has inherently better thermal and long-term stability compared to mirror-based optics.

Claims

1. In a flow cytometry system, excitation optics for delivering excitation light beams to a cytometry flow cell, comprising:

a plurality of light sources producing light beams of different wavelengths;

a mounted set of dispersive prism elements arranged in sequence so that all of the light beams from said sources pass through each of the prism elements in succession and are refracted by different amounts by said prism elements, input positions and angles of the light beams selected so that the refracted beams from the final prism element in the sequence substantially overlap are nearly parallel to one another and elliptical; and

an objective lens focusing the beams from the final prism element to closely spaced spots within the cytometry flow cell.

2. The cytometry excitation optics of claim 1 wherein the nearly parallel refracted beams have angular separations at the output surface of the final prism element of less than 1°

.

3. The cytometry excitation optics of claim 1 wherein the light beams are delivered to the mounted set of dispersive prism elements via optical fibers with mounted output couplers in fixed relation to the prism elements.

4. The cytometry excitation optics of claim 1 wherein the light beams are delivered to the mounted set of dispersive prism elements directly, the light sources being mounted in fixed relation to the prism elements.

5. The cytometry excitation optics of claim 1 wherein at least one of the light beams is delivered to the mounted set of dispersive prism elements via mounted optical wedge pieces directing that beam from a mounted light source to the prism elements, the light source and wedge pieces being mounted in fixed relation to the prism elements.

6. The cytometry excitation optics of claim 1 wherein the number of light sources, light beams and wavelengths is three.

7. The cytometry excitation optics of claim 6 wherein one of the light beams has a wavelength in a range from about 395 nm to 420 nm.

8. The cytometry excitation optics of claim 6 wherein one of the light sources is an argon laser providing a light beam of 488 nm wavelength.

9. The cytometry excitation optics of claim 6 wherein one of the light beams has a wavelength in a range from about 633 nm to 640 nm.

10. The cytometry excitation optics of claim 1 wherein the number of prism elements is four.

11. The cytometry excitation optics of claim 10 wherein each of the prism elements is a distinct isosceles triangular prism with a specified apex angle.

12. The cytometry excitation optics of claim 11 wherein the prism apex angle is 29°

, wherein each of the first and third prism elements is mounted apex up at a 31.233°

orientation angle between its prism output surface and vertical and each of the second and fourth prism elements is mounted apex down at a 6.47°

orientation angle between its prism output surface and vertical, wherein the centers of the prism output surfaces have coordinates (−

75.0, 19.1), (−

50.0, 11.2), (−

25.0, 7.9) and (0.0, 0.0), and wherein the prisms are composed of a flint glass material substantially like Schott optical glass LF5 (581409).

13. The cytometry excitation optics of claim 12 wherein a first beam of wavelength 405 nm has a −

3.713°

entry angle and (−

79.82, 23.32) entry coordinates at the first prism element, a second beam of wavelength 488 nm has a 0.0°

entry angle and (−

81.44, 22.40) entry coordinates, and a third beam of wavelength 640 nm has a +3.209°

entry angle and (−

82.88, 21.57) entry coordinates.

14. The cytometry excitation optics of claim 1 wherein the number of light sources include an argon ion laser providing a light beam of 351 nm with an input angle of 6.904°

.

15. The cytometry excitation optics of claim 11 wherein first and fourth prisms are mounted apex up and second and third prisms are mounted apex down, the prisms positioned and oriented such that input and output of one beam through the set of prisms are collinear.