Real-time label-free high-throughput cell screening in flow
A label-free imaging-based flow cytometer that measures size and cell protein concentration simultaneously is disclosed. Cell protein concentration adds a parameter to cell classification that improves the specificity and sensitivity of flow cytometers without the requirement of cell labeling. The system uses coherent dispersive Fourier transform to perform phase imaging at flow speeds as high as a few meters per second. To retrieve cell information in real-time, an analog signal processing system based on quadrature phase demodulation is described.
1. A system for phase contrast imaging of cells or dielectric particles in flow, comprising:
an interferometer configured to map a phase image of the cells or dielectric particles into a spectrum of broadband optical pulses;
a serial time-encoded amplified microscopy (STEAM) module; and
a photodetector coupled to the interferometer and STEAM module;
wherein the interferometer and STEAM module generate a coherent-STEAM output configured to simultaneously measure a size and optical phase shift of the cells or dielectric particles.
2. A system as recited in claim 1 , wherein the coherent-STEAM output is configured to simultaneously measure a size and optical density of the cells or dielectric particles.
3. A system as recited in claim 1 , wherein the coherent-STEAM output is configured to simultaneously measure a size and protein concentration of the cells.
4. A system as recited in claim 3 , wherein the coherent-STEAM output is configured for high-speed phase microscopy for label-free single-cell classification.
5. A system as recited in claim 1 , wherein the STEAM module is configured to chirp, stretch and amplify each optical pulse so that different wavelength components reach the photodetector serially.
6. A system as recited in claim 5 , wherein the STEAM module comprises a Raman amplifier and a dispersive fiber to perform dispersive Fourier transform.
7. A system as recited in claim 1 , further comprising:
one or more optical reflective optical components coupled to the interferometer and STEAM module.
8. A system as recited in claim 7 , wherein the one or more optical components comprise reflection diffraction gratings and parabolic mirrors.
9. A system as recited in claim 1 , wherein the interferometer comprises a Michelson interferometer.
10. A system as recited in claim 1 , further comprising:
a module for performing analog IQ demodulation of phase images of the coherent-STEAM output.
11. A system as recited in claim 1 , further comprising:
a module for performing digital signal processing for interferometric STEAM.
12. A system as recited in claim 11 , the digital signal processing module configured for performing the steps of:
digitizing and recording the coherent-STEAM output signal;
saving each optical pulse in the output signal separately as a frame for further processing;
generating an analytic form of each pulse and extracting a phase component of the analytic form; and
combining phase line images generated from subsequent frames to form a spatial map of optical path difference.
13. A system as recited in claim 12 , further comprising:
extracting a refractive index contrast between a cell and surrounding liquid as a function of the spatial map of optical path difference.
14. A system as recited in claim 1 , further comprising:
a module for performing analog signal processing as a function of down-conversion of high-frequency spectral components of the Coherent-STEAM output.
15. A system as recited in claim 14 , wherein said analog signal processing module is configured to apply quadrature phase demodulation to retrieve cell measurements in real-time.
16. A system as recited in claim 15 , the analog signal processing module configured for performing the steps of:
splitting the coherent-STEAM output signal into two signals;
mixing the two split signals with two phase-shifted sinusoidal signals; and
filtering a baseband component from the mixed signals.
17. A system as recited in claim 14 , wherein said analog signal processing module comprises an FPGA comprising:
an argument calculator;
first in, first out (FIFO); and
an unwrapper.
18. A method for phase contrast imaging of cells or dielectric particles in flow, comprising:
using an interferometer, mapping a phase image of the cells or dielectric particles into a spectrum of broadband optical pulses;
chirping, stretching and amplifying each optical pulse so that different wavelength components are serially registered on a photodetector as a coherent serial time-encoded amplified microscopy (Coherent- STEAM) output; and
simultaneously measuring a size and optical phase shift of the cells or dielectric particles.
19. A method as recited in claim 18 , further comprising simultaneously measuring a size and optical density of the cells or dielectric particles.
20. A method as recited in claim 18 , further comprising simultaneously measuring a size and protein concentration of the cells.
21. A method as recited in claim 20 , wherein the coherent-STEAM output is configured for high-speed phase microscopy for label-free single-cell classification.
22. A method as recited in claim 18 , wherein the STEAM module comprises a Raman amplifier and a dispersive fiber to perform dispersive Fourier transform.
23. A method as recited in claim 18 , further comprising:
performing analog IQ demodulation of phase images of the coherent-STEAM output.
24. A method as recited in claim 18 , further comprising:
performing digital signal processing for interferometric STEAM.
25. A method as recited in claim 24 , further comprising:
digitizing and recording the coherent-STEAM output signal;
saving each optical pulse in the output signal separately as a frame for further processing;
generating an analytic form of each pulse and extracting a phase component of the analytic form; and
combining phase line images generated from subsequent frames to form a spatial map of optical path difference.
26. A method as recited in claim 25 , further comprising:
extracting a refractive index contrast between a cell and surrounding liquid as a function of the spatial map of optical path difference.
27. A method as recited in claim 18 , further comprising:
performing analog signal processing as a function of down-conversion of high-frequency spectral components of the Coherent-STEAM output.
28. A method as recited in claim 27 , wherein performing analog signal processing comprises applying quadrature phase demodulation to retrieve cell measurements in real-time.
29. A method as recited in claim 28 , further comprising:
splitting the coherent-STEAM output signal into two signals;
mixing the two split signals with two phase-shifted sinusoidal signals; and
filtering a baseband component from the mixed signals.