Trajectory-based triggering system for hyperspectral imaging flow cytometer
A hyperspectral imaging flow cytometer can acquire high-resolution hyperspectral images of particles, such as biological cells, flowing through a microfluidic system. A trajectory-based triggering system can be used that will only trigger the acquisition of a hyperspectral image when an appropriate particle or cell is crossing an imaging line, thereby saving valuable resources and time. The hyperspectral imaging flow cytometer can provide detailed spatial maps of multiple emitting species, cell morphology information, and state of health. An optimized system can image about 20 cells per second. The hyperspectral imaging flow cytometer enables many thousands of cells to be characterized in a single session.
1. A hyperspectral imaging flow cytometer, comprising:
a microfluidic flow system for injecting a sample of fluorescent particles into a channel, directing the particles to flow through an imaging field in the channel, and sorting the particles into separate bins in response to an analysis of an acquired image of each particle;
a trajectory-based triggering system for obtaining a first image of a particle a first time at a first location in the channel, obtaining a second image of the particle at a later second time at a second location downstream in the channel, predicting a third time and a lateral location at which the particle will cross an imaging line downstream from the first and second locations in the channel, and providing a trigger,
a hyperspectral confocal imaging system having a focal plane downstream from the first and second locations for laterally scanning a focused laser beam along the imaging line at the third time with the laser scanning centered on the predicted lateral location in the channel and acquiring a two-dimensional hyperspectral image of fluorescence emitted by the particle by rastering the focused laser beam along the imaging line as the particle flows through the predicted lateral location in response to the trigger; and
an analyzer for real-time multivariate analysis of the acquired hyperspectral image of the particle to direct the microfluidic system to sort the particle into a bin.
2. The hyperspectral imaging flow cytometer of claim 1 , wherein the particles comprise biological cells.
3. The hyperspectral imaging flow cytometer of claim 1 , wherein the particles comprise fluorescently tagged beads.
4. The hyperspectral imaging flow cytometer of claim 1 , wherein the particles comprise at least two emitting species.
5. The hyperspectral imaging flow cytometer of claim 1 , wherein the flow velocity of the particles in the channel is greater than 50 μm/sec.
6. The hyperspectral imaging flow cytometer of claim 1 , wherein the directing of particles in the channel comprises hydrodynamic focusing.
7. The hyperspectral imaging flow cytometer of claim 1 , wherein the trajectory-based triggering system comprises a machine vision system.
8. The hyperspectral imaging flow cytometer of claim 1 , wherein field-of-view of the confocal imaging system is less than 50 μm.
9. The hyperspectral imaging flow cytometer of claim 1 , wherein the confocal imaging system acquires hyperspectral images at a rate of approximately 20 particles per second or greater.
10. The hyperspectral imaging flow cytometer of claim 1 , wherein the multivariate analysis comprises Classical Least Squares, Multivariate Curve Resolution, or Principle Component Analysis.
11. The hyperspectral imaging flow cytometer of claim 1 , wherein the particle is sorted using spectral information from the multivariate analysis of the acquired hyperspectral image of the particle.
12. The hyperspectral imaging flow cytometer of claim 1 , wherein the particle is sorted using the spatial information from the multivariate analysis of the acquired hyperspectral image of the particle.
13. The hyperspectral imaging flow cytometer of claim 1 , wherein the sorting the particles into separate bins comprises dielectrophoretic sorting.