Method and system for spectral analysis of biological materials using stimulated cars

• US 20060066848A1
• Filed: 09/30/2004
• Published: 03/30/2006
• Est. Priority Date: 09/30/2004
• Status: Active Grant

• Current Assignee: Chromaplex, Inc.
• Original Assignee: Chromaplex, Inc.
• Inventors: Frankel, Robert
• Granted Patent: US 7,289,203 B2
• Time in Patent Office: Days
• US Class Current: 356/301
• CPC Class Codes: G01J 3/44 Raman spectrometry; Scattering spectrometry ; Fluorescence spectrometry
• CPC Class Codes: G01N 2021/653 Coherent methods [CARS]
• CPC Class Codes: G01N 2021/655 Stimulated Raman
• CPC Class Codes: G01N 21/65 Raman scattering
• CPC Class Codes: G01N 21/658 enhancement Raman, e.g. surface plasmons

Abstract

A CARS system and method for probing a Raman signature of a sample are described. A short femtosecond pulse from one or more lasers is split into two pulses, a stimulus pulse and a probe pulse, whereby the probe pulse is time-delayed with respect to the stimulus pulse. Both pulses can be phase- and polarization-modulated. The stimulus pulse excites a vibronic level in the sample and the probe pulse probes molecular Raman transitions in the sample. A difference in the signals with and without excitation can be used to determine on which molecule a bond is most likely located. This will allow an accurate and sensitive determination of the presence of specific molecules in the sample. The system and method can be used to analyze biological samples and to discriminate between molecules having overlapping Raman signatures.

Claims

1. A CARS system for probing a Raman signature of a sample, comprising

at least one laser producing a femtosecond laser pulse;

a beam splitter splitting the femtosecond laser pulse into a stimulus pulse and a probe pulse;

a first spectral phase modulator modulating a phase or a polarization, or both, of the stimulus pulse;

a second spectral phase modulator modulating a phase or polarization, or both, of the probe pulse;

an optical delay line for time-delaying the modulated probe pulse with respect to the stimulus pulse; and

a spectral analyzer that detects the Raman signature of the sample in response to the probe pulse and after stimulation of the sample by the stimulus pulse.

2. The CARS system of claim 1, wherein the optical delay line provides a variable time delay between the stimulus pulse and the probe pulse at the sample.

3. The CARS system of claim 2, wherein the optical delay line is a free-space delay line.

4. The CARS system of claim 1, wherein the at least one laser comprises a Ti:

S laser.

5. The CARS system of claim 1, wherein at least one of the phase modulators comprises a liquid crystal.

6. The CARS system of claim 1, wherein at least one of the phase modulators comprises a grating operating as a pulse stretcher.

7. The CARS system of claim 1, wherein at least one of the phase modulators comprises a grating operating as a pulse compressor.

8. The CARS system of claim 1, wherein the sample comprises at least two different types of molecules having Raman signatures.

9. The CARS system of claim 1, wherein the spectral analyzer detects Raman signatures of the sample in response to the probe pulse both with and without stimulation of the sample by the stimulus pulse and computes a difference between the Raman signatures detected with and without stimulation.

10. The CARS system of claim 1, wherein the at least one laser is a mode-locked laser.

11. The CARS system of claim 1, comprising at least two lasers providing synchronized mode-locked femtosecond laser pulses incident on the beam splitter.

12. A method for identifying molecules in a molecular system based on a stimulated CARS signature, comprising:

a. providing a first optical probe pulse and measuring a first CARS response signal from the molecular system;

b. providing an optical stimulus pulse and a second optical probe pulse that is time-delayed with respect to the stimulus pulse;

c. measuring with the second optical probe pulse a second CARS response signal from the molecular system;

d. subtracting the first CARS response signal from the second CARS response signal to form a difference signal;

e. repeating steps a) through e) with a different optical stimulus pulse; and

f. identifying molecules and a concentration of the molecules in the molecular system based on the difference signal.

13. The method of claim 12, wherein a non-zero difference signal indicates a CARS signal from a molecular bond of a molecule that is different from a molecular bond stimulated by the stimulus pulse.

14. The method of claim 12, wherein the optical time delay is variable.

15. The method of claim 14, wherein the optical time delay is produced by a free-space delay line.

16. The method of claim 12, wherein the first optical probe pulse, the second optical probe pulse and the stimulus pulse are produced by at least two lasers.

17. The method of claim 12, wherein the first optical probe pulse, the second optical probe pulse and the stimulus pulse are produced by a single laser.

18. The method of claim 12, wherein the second optical probe pulse and the stimulus pulse are produced from the same laser pulse.

19. The method of claim 16, wherein the laser comprises a mode-locked Ti:

S laser.

20. The method of claim 12, wherein at least one of a phase and a polarization of the stimulus pulse are modulated.

21. The method of claim 12, wherein at least one of a phase and a polarization of at least one of the first or second probe pulse are modulated.

22. The method of claim 12, wherein the sample comprises at least two different types of molecules having CARS signatures.

23. The method of claim 12, further labeling nanoparticles with Raman-active molecules to provide Raman tags which enhance the CARS response signal.

24. The method of claim 23, wherein the Raman tags bond to biological materials to be probed.