Autofluorescence enhanced photothermal infrared spectroscopy
Methods and systems described herein detect autofluorescence of a sample. These methods and systems obviate the need for addition of fluorophores to samples to create IR absorption.
1. A method for performing infrared imaging of a sample, the method comprising:
illuminating a first region of the sample with an infrared source that generates a modulated infrared beam;
illuminating a second region of the sample at least partially overlapping the first region with a beam of excitation radiation to excite autofluorescent emission;
detecting at least a portion of the autofluorescent emission from the second region by at least one detector as detected autofluorescent emission;
obtaining a first measurement of autofluorescent emission of the second region with a first value of infrared beam energy;
obtaining a second measurement of autofluorescent emission of the second region with a second value of infrared beam energy; and
constructing an output indicative of infrared absorption of the sample using the first and the second measurements of autofluorescent emission.
2. The method of claim 1 , wherein the at least one detector is an array-based detector.
3. The method of claim 1 , wherein the at least one detector is a single-point detector.
4. The method of claim 1 , wherein a source of the beam of excitation radiation is a light emitting diode (LED) source.
5. The method of claim 1 , wherein a source of the beam of excitation radiation is a laser source.
6. The method of claim 1 , wherein the illuminating of the first region and illuminating the second region is performed using a counter-propogating geometry.
7. The method of claim 1 , wherein the illuminating of the first region and illuminating the second region is performed using a co-propogating geometry.
8. The method of claim 7 , wherein the sample is opaque.
9. The method of claim 1 , wherein detecting the detected autofluorescent emission comprises detecting a target class selected from the group consisting of: NAD(P)H bound, NAD(P)H free, fatty acids, vitamins, flavins, proteins, porphyrins, and chlorophyll.
10. The method of claim 1 , wherein constructing the output comprises substantially maximizing transmission of a peak amplitude of an autofluorescent emission spectrum of the sample.
11. An apparatus for performing infrared imaging of a sample,
the apparatus comprising:
an excitation radiation source configured to illuminate a first region of the sample with a beam of excitation radiation to excite autofluorescent emission in the sample;
a modulated infrared source configured to illuminate a second region of the sample at least partially overlapping the first region with a modulated infrared beam to create an infrared illuminated region of the sample;
at least one detector configured to capture at least a portion of the autofluorescent emission from the infrared illuminated region of the sample and obtain a first measurement of autofluorescent emission of the second region with a first value of infrared beam energy and obtain a second measurement of autofluorescent emission of the second region with a second value of infrared beam energy; and
a demodulator configured to construct a signal indicative of infrared absorption of the second region of the sample using the first and second measurements of autofluorescent emission.
12. The apparatus of claim 11 , wherein the at least one detector is an array-based detector.
13. The apparatus of claim 11 , wherein the at least one detector is a single-point detector.
14. The apparatus of claim 11 , wherein the excitation radiation source is a light emitting diode (LED) source.
15. The apparatus of claim 11 , wherein the excitation radiation source is a laser source.
16. The apparatus of claim 11 , wherein the illuminating of the first region and the illuminating of the second region is performed using a counter-propogating geometry.
17. The apparatus of claim 11 , wherein illumination of the first region and the illumination of the second region is performed using a co-propogating geometry.
18. The apparatus of claim 17 , wherein the sample is opaque.
19. The apparatus of claim 11 , further comprising a stage configured to hold the sample.
20. The apparatus of claim 19 , wherein the stage is movable relative to at least one of the beam of infrared illumination and the beam of excitation radiation.