Imaging apparatus and method

• US 6,594,011 B1
• Filed: 07/11/2000
• Issued: 07/15/2003
• Est. Priority Date: 07/11/2000
• Status: Expired due to Term

• Current Assignee: Maven Biotechnologies, LLC
• Original Assignee: Maven Technologies, LLC
• Inventors: Kempen, Lothar U.
• Primary Examiner(s): Pham, Hoa Q.
• Application Number:
  US09/614,503
• Time in Patent Office: 1,099 Days
• Field of Search: 356/364-369, 356/445, 356/446, 356/128, 356/136, 422/82.08, 422/82, 422/11, 435/6, 435/7.1, 435/808, 435/288.7, 436/517, 436/805, 436/527
• US Class Current: 356/369
• CPC Class Codes: G01N 21/21 Polarisation-affecting properties G01N21/19 takes precedence
• CPC Class Codes: G01N 21/253 for batch operation, i.e. multisample apparatus analytical automats G01N35/00
• CPC Class Codes: G01N 21/552 Attenuated total reflection
• CPC Class Codes: Y10S 436/805 Optical property

Abstract

Imaging apparatus and method which uses change of polarization state of a light beam passed through a total internal reflection structure by a single reflection at a TIR surface in which a specimen is placed in the evanescent field associated with the total internal reflection of the light beam, the specimen being the subject of biological, chemical or genetic investigation.

Claims

1. An imaging apparatus for imaging a specimen array within the evanescent field present upon reflection of a beam of light at a TIR surface comprising;

a polarized light source member emitting a polarized, extended beam of light;

a TIR structure having a TIR surface, the light from said polarized light source member being reflected only a single time by the TIR surface, the specimen being within the evanescent field associated with the total internal reflection at the TIR surface said specimen causing spatially distributed polarization changes in the beam'"'"'s cross-section; and

a polarization-sensitive, two-dimensional array detector, said detector resolving the light beam reflected from the TIR surface as an image of the spatially distributed polarization changes caused by the specimen.

2. Apparatus as in claim 1 wherein said polarized light source member comprises a quasi-monochromatic light source of moderate bandwidth.

3. Apparatus as in claim 2 wherein said quasi-monochromatic light source of moderate bandwidth is a light-emitting diode (LED).

4. Apparatus as in claim 2 wherein said quasi-monochromatic light source of moderate bandwidth is a superluminescent diode (SLD).

5. Apparatus as in claim 2 wherein said quasi-monochromatic light source of moderate bandwidth has an optical bandwidth with a full width half maximum between 5 nm and 60 nm.

6. Apparatus as in claim 2 wherein said quasi-monochromatic light source of moderate bandwidth comprises an incandescent source and an optical filter, the light emitted from said light source passing through said filter, said filter limiting the wavelengths of the light transmitted through said optical filter such as to constitute quasi-monochomatic light of moderate bandwidth.

7. Apparatus as in claim 1 wherein said polarized light source member comprises a laser emitting substantially coherent light, and further comprising an optical diffuser mechanically attached to a mechanical actuator, the light emitted from said laser passing through said diffuser, said diffuser being moved with respect to said laser by said actuator, the movement of said diffuser with respect to said laser creating fluctuations in the speckle pattern of light detected by said detector, said fluctuations being adapted to remove speckle effects from the light detected by said detector.

8. Apparatus as in claim 7, wherein said mechanical actuator is a motor rotating said optical diffuser.

9. Apparatus as in claim 1, wherein said polarized light source member comprises a beam forming system, said beam forming system causing the light emerging from said polarized light source member to be collimated.

10. Apparatus as in claim 1, wherein said polarized light source comprises an optical polarizer.

11. Apparatus as in claim 1 wherein said polarized light source member comprises an optical retarder, said retarder introducing an optical phase shift between two orthogonal components of light passing through said retarder.

12. Apparatus as in claim 11, wherein said optical retarder is set up to be controllably rotated by a motor.

13. Apparatus as in claim 11, wherein said optical retarder is set up to change its retardance according to an externally introduced physical parameter.

14. Apparatus as in claim 1, wherein said TIR structure comprises an optical prism.

15. Apparatus as in claim 14, wherein the light from said polarized light source member is directed to enter said prism along an axis perpendicular to one of the sides of said prism.

16. Apparatus as in claim 14, wherein the light reflected from said TIR surface exits said prism along an axis perpendicular to one of the sides of said prism.

17. Apparatus as in claim 1, wherein said specimen array comprises a two dimensional array of multiple fields comprising biomolecular substances.

18. Apparatus as in claim 17, wherein said biomolecular substances are proteins.

19. Apparatus as in claim 17, wherein said biomolecular substances are peptides.

20. Apparatus as in claim 17, wherein said biomolecular substances are polynucleotide sequences.

21. Apparatus as in claim 1, wherein said polarization-sensitive, two-dimensional array detector comprises an optical polarizer.

22. Apparatus as in claim 21, wherein said polarizer is set up to be controllably rotated by a motor.

23. Apparatus as in claim 1, wherein said polarization-sensitive, two-dimensional array detector comprises a two-dimensional CCD array.

24. Apparatus as in claim 1, wherein said polarization-sensitive, two-dimensional array detector comprises a two-dimensional photodiode array.

25. Apparatus as in claim 1, further comprising a signal processing member, said signal processing member being connected to said polarization-sensitive, two-dimensional array detector, said signal processing member processing the signal from said polarization-sensitive, two-dimensional array detector to obtain a two-dimensional representation of the optical phase shifts occurring in the specimen.

26. A method of imaging a chemical specimen array comprising;

passing an extended polarized light beam into a TIR structure for reflection at a TIR surface of the TIR structure and exiting after a single reflection at said TIR surface;

a specimen being in the evanescent field of the reflected light beam;

detecting the spatially distributed change in polarization state caused by the array; and

processing the spatially distributed change in polarization state information detected to provide an image of the specimen array.

27. The method of claim 26 wherein said specimen array comprises a plurality of discrete specimen spots and said image is provided for each of said discrete specimen spots.

28. A method of characterizing a two-dimensionally distributed chemical specimen array in the evanescent field associated with total internal reflection of a beam comprising;

directing an extended beam of light of known polarization state at a total internal reflection surface, the beam undergoing a single total internal reflection at the total internal reflection surface;

determining the spatially distributed change in the beam'"'"'s polarization state caused by the chemical specimen array in the evanescent field; and

processing the spatially distributed change in polarization state information detected to provide an image of the specimen array.

29. The method of claim 28 further comprising using the spatially distributed change in the beam'"'"'s polarization state, determining two-dimensionally distributed presence or properties or both of constituents of the chemical specimen array.

30. The method of claim 29 wherein the chemical specimen array is in a micro-titer plate comprising;

resolving the spatially distributed polarization changes in the light beam for matching positions in the micro-titer plate; and

analyzing the polarization changes to determine desired characteristics in each position.

31. The method of claim 29 wherein the chemical specimen array is a series of discrete specimen spots;

and

the method comprises analyzing the polarization state changes to determine the binding characteristics of each discrete specimen spot in the array.

32. The method of claim 28 wherein a chemical specimen array having no molecular tagging is placed with the evanescent field associated with the beam.