DATA COLLECTION SYSTEM AND METHOD FOR A FLOW CYTOMETER

• US 20100302536A1
• Filed: 06/02/2009
• Published: 12/02/2010
• Est. Priority Date: 06/02/2009
• Status: Active Grant

• Current Assignee: Accuri Cytometers, Inc. (Becton, Dickinson & Co)
• Original Assignee: Accuri Cytometers, Inc. (Becton, Dickinson & Co)
• Inventors: Clare, Rogers E., Rich, Collin A., Ball, Jack T.
• Granted Patent: US 8,004,674 B2
• Time in Patent Office: Days
• US Class Current: 356/317
• CPC Class Codes: G01J 3/4406 Fluorescence spectrometry

Abstract

A system for a flow cytometer that collects data for a sample prepared with a plurality of fluorochromes that includes a fixed gain detection system that collects data for a plurality of fluorescence channels, fluorochrome compensation factors for a plurality of fluorochromes types, and a computer system that has an interface that gathers fluorochrome information of the sample and an analysis program that compensates for spectral spillover in the collected data. The fixed gain detection system preferably has a wide dynamic range. A fluorochrome compensation factor preferably remains constant for a fixed gain detection system. The analysis program preferably uses the fluorochrome compensation factors to compensate for spectral spillover.

Claims

1. A system for a flow cytometer that collects data for a sample prepared with a plurality of fluorochromes comprising:

a fixed gain detection system that collects data for a plurality of fluorescence channels, the detector having a wide dynamic range;

fluorochrome compensation factors for a plurality of fluorochromes types, wherein a fluorochrome compensation factor remains constant for the fixed gain detection system; and

a computer system that includes;

an interface that gathers fluorochrome information of the sample; and

an analysis program that compensates for spectral spillover in the collected data, using the fluorochrome compensation factors.

2. The system of claim 1, wherein the detection system includes multiple detectors for collecting fluorescence over a wide spectrum of light, the individual detectors measuring light for a single fluorescence channel.

3. The system of claim 1, wherein the compensation factors are mathematical descriptions of a relationship of spectral spillover for the fixed gain detection system, the relationship being a substantially linear function dependent on fluorescence type.

4. The system of claim 3, wherein the compensation factors are stored within the computer system as a pre-calculated, fluorochrome-specific spectral compensation value.

5. The system of claim 4, wherein a compensation factor is associated with a calibrated slope and y-intercept of a two fluorescence channel relationship for the fixed gain detector system.

6. The system of claim 4, wherein the fluorochrome information is associated with the types of fluorochromes within the sample.

7. The system of claim 6, wherein the interface is a computer graphical interface for human entry of fluorochrome information of the sample.

8. The system of claim 6, wherein a computer detectable device is sensed by the computer interface to determine the type of fluorochrome information.

9. The system of claim 6, wherein fixed gain describes a constant voltage and gain.

10. The system of claim 9, wherein the fixed gain detection system collects data that is an absolute measurement in photometric units.

11. The system of claim of 9, wherein particles of the sample that are sized 1 micron to 100 microns are detectable in the wide dynamic range.

12. The system of claim 9, wherein the wide dynamic range is at least a six decade span.

13. The system of claim 9, wherein the fixed gain detection system is not alterable by an experimenter during a single fluorochrome calibration of a sample.

14. A system for a flow cytometer comprising:

a fixed gain detection system including;

a detector that receives photonic inputs from an interrogation zone of the flow cytometer to sense a plurality of channels of fluorescence and that produces an analog signal, the detector having a wide dynamic range; and

an analog-to-digital converter (ADC) coupled to the detector and that converts an analog signal to a digital signal, the ADC having a high bit resolution; and

an analysis program that compensates for spectral spillover for sampled data, wherein the software uses stored fluorochrome compensation factors that are static for the detection system.

15. The system of claim 14, further including an amplifier coupled to the detector.

16. The system of claim 14, wherein wide dynamic range is at least six decades.

17. The system of claim 14, wherein the analog signal of the detector is an absolute measurement of photon counts.

18. The system of claim 14, wherein the software program includes an interface for entry of the fluorochrome information of a sample.

19. The system of claim 18, wherein the analysis program calculates expected spillover in a second fluorescence channel using a stored fluorochrome compensation factor and a measurement from a first fluorescent channel, and the analysis program subtracts the expected spillover from a measurement of the second fluorescence channel.

20. The system of claim 19, wherein the detection system includes a plurality of detectors and a plurality of analog-to-digital converters, where a detector is coupled to an ADC and measures a single fluorescence channel.

21. The system of claim 19, wherein the detection system includes a plurality of analog-to-digital converters coupled to a detector, wherein an individual ADC handles a single fluorescence channel.

22. A method of collecting data in a flow cytometer system comprising:

acquiring fluorochrome information for a sample through a computer interface;

collecting sample data with a fixed gain detection system of the flow cytometer;

accessing stored fluorochrome compensation factors associated with the acquired fluorochrome information; and

compensating for spectral spillover using the accessed fluorochrome compensation factors.

23. The method of claim 22, wherein the step of compensating for spectral spillover includes:

computing expected spectral spillover using a fluorochrome compensation factor; and

subtracting the expected spectral spillover from a fluorescence channel.

24. The method of claim 23, wherein the compensation is accomplished without requiring a single fluorochrome sample to be examined for calibration of the fixed gain detection system.

25. The method of claim 23, including calculating molecules of equivalent soluble fluorophore (MESF) from a calibrated intensity measurement of an excitation laser of the flow cytometer and from the sample data collected by the fixed gain detection system.