MULTI-CHANNEL LOCK-IN AMPLIFIER SYSTEM AND METHOD

• US 20080221805A1
• Filed: 03/10/2008
• Published: 09/11/2008
• Est. Priority Date: 03/09/2007
• Status: Abandoned Application

• Current Assignee: Sensortec Limited
• Original Assignee: Sensortec Limited
• Inventors: Andrews, David Richard
• Application Number:
  US12/045,397
• Publication Number:
  US 20080221805A1
• Time in Patent Office: Days
• US Class Current: 702/19
• CPC Class Codes: G01N 15/1023 Microstructural devices for non-optical measurement
• CPC Class Codes: G01N 15/1031 by measuring electrical or magnetic effects
• CPC Class Codes: G01N 15/1056 Microstructural devices for other than electro-optical measurement for electro-optical measurement G01N15/1484

Abstract

A multi-channel lock-in amplifier system for use in cell analysis is disclosed. The system may include a cartridge having one or more flow cells with each flow cell containing a cell for analysis. An oscillating electric field may be applied across each flow cell at one or more excitation frequencies in order to detect the responses of the cell either in electrical impedance at frequencies that provide a non-linear response.

Claims

1. A multi-channel lock-in amplifier system for analyzing a biological sample comprising:

an electrical interface to connect to electrodes of a microfluidic unit, the microfluidic unit containing the biological sample;

a first waveform synthesizer configured to generate at least one test signal having at least one test frequency to apply to the electrodes to create an electric field in the microfluidic unit;

a plurality of lock-in amplifier (LIA) circuits each configured to;

apply a receiving oscillating signal having a receiving frequency to the electrodes;

measure a voltage signal and a current signal generated in the microfluidic unit as the biological sample passes through the electric field; and

multiply the voltage signal and the current signal by the receiving oscillating signal having the receiving frequency to create a plurality of composite signals, the receiving frequency comprising a harmonic of the test frequency;

a processor to configured to;

calculate impedance data of the biological sample as a function of the plurality of composite signals;

retrieve historical impedance data corresponding to the biological sample from a memory;

compare the calculated impedance data to the historical impedance data to determine a type of the biological sample; and

a display to generate the calculated impedance for display.

2. The multi-channel lock-in amplifier system of claim 1 wherein multiplying the voltage signal and the current signal by the receiving oscillating signal having the receiving frequency enables the detection of a non-linear response from the biological sample.

3. The multi-channel lock-in amplifier system of claim 1 wherein each of the plurality of lock-in amplifier (LIA) circuits comprises:

a second waveform synthesizer to generate the receiving oscillating signal; and

a plurality of mixers each configured to one of the voltage signal and the current signal by the receiving oscillating signal to create the plurality of composite signals.

4. The multi-channel lock-in amplifier system of claim 3 wherein the receiving oscillating signal comprises a synthesized output component and a phase shifted synthesized output component, and wherein:

a first mixer is configured to multiply the voltage signal by the synthesized output component to create a first composite signal;

a second mixer is configured to multiply the current signal by the synthesized output component to create a second composite signal;

a third mixer is configured to multiply the voltage signal by the phase shifted synthesized output component to create a third composite signal; and

a fourth mixer is configured to multiply the current signal by the phase shifted synthesized output component to create a fourth composite signal.

5. The multi-channel lock-in amplifier system of claim 1 wherein the historical data corresponds to histogram data of voltage and current data for the biological sample.

6. The multi-channel lock-in amplifier system of claim 1 wherein the first waveform synthesizer is configured to generate a first test signal and a second test signal to apply to the electrodes to create an electric field in the microfluidic unit, the first test signal having a first test frequency and the second test signal having a second test signal, and wherein the receiving frequency comprises a sum of the first and second test frequencies or a difference of the first and second test frequencies.

7. The multi-channel lock-in amplifier system of claim 1 further comprising a user interface to control the LIA circuit to generate the receiving oscillating signal having the receiving frequency in response to input from a user.

8. The multi-channel lock-in amplifier system of claim 7 wherein the test frequency is an excitation frequency and wherein the processor is configured to select the receiving frequency of the receiving oscillating signal from the group consisting of a sub-harmonic, a fundamental, and a harmonic.

9. The multi-channel lock-in amplifier system of claim 1 wherein the processor is further configured to compare the calculated impedance data to the historical impedance data to determine if a disease is present in the biological sample.

10. A point of care system comprising a multi-channel lock-in amplifier (MCLIA) for analyzing a biological sample, the MCLIA comprising:

an electrical interface to connect to electrodes of a microfluidic unit, the microfluidic unit containing the biological sample;

a first waveform generator configured to generate at least one excitation signal having an excitation frequency to apply to the electrodes to create an electric field in the microfluidic unit;

a plurality of lock-in amplifier (LIA) circuits each configured to;

to measure a voltage signal and a current signal generated in the microfluidic unit as the biological sample passes through the electric field; and

to multiply the voltage signal and the current signal by a receiving oscillating signal having a receiving frequency to create a plurality of composite signals, the receiving frequency comprising a harmonic of the excitation frequency; and

a processor comprising modules executable on the processor, the modules comprising;

a detection module configured to detect the connection of the microfluidic unit to the MCLIA to display a menu to a user via a user interface;

a frequency selection module configured to set the excitation frequency in response to input from the user via the user interface;

a harmonic frequency selection module configured to set the receiving frequency to a harmonic of the excitation frequency;

a sampling module configured to sample current data and voltage data from the plurality of composite signals;

a data collection module configured to collect the sampled data comprising voltage and current for linear and non-linear responses and to store the sampled voltage and current data in a memory;

a calculation module configured to calculate impedance of the biological sample as a function of the sampled voltage and current data; and

a comparison module configured to compare the calculated impedance to historical linear and non-linear data to determine a type of the biological sample.

11. The system of claim 10 wherein multiplying the voltage signal and the current signal by a receiving oscillating signal having the receiving frequency enables the detection of a non-linear response from the biological ample.

12. The system of claim 10 wherein each of the plurality of LIA circuits comprises:

a second waveform generator to generate the receiving oscillating signal; and

a plurality of mixers each configured to multiple one of the voltage signal and the current signal by the receiving oscillating signal to create the plurality of composite signals.

13. The system of claim 12 wherein the receiving oscillating signal comprises a synthesized output component and a phase shifted synthesized output component, and wherein:

a first mixer configured to multiply the voltage signal by the synthesized output component to create a first composite signal;

a second mixer configured to multiply the current signal by the synthesized output component to create a second composite signal;

a third mixer configured to multiply the voltage signal by the phase shifted synthesized output component to create a third composite signal; and

a fourth mixer configured to multiply the current signal by the phase shifted synthesized output component to create a fourth composite signal.

14. The system of claim 10 further comprising a histogram module configured to generate a histogram based on the historical linear and non-linear data voltage current data, and wherein the comparison module compares the calculated impedance to historical linear and non-linear data defined by the histogram to determine the type of the biological sample.

15. The system of claim 10 wherein the first waveform generator is configured to generate a first excitation signal and a second excitation signal to apply to the electrodes to create an electric field in the microfluidic unit, the first excitation signal having a first excitation frequency and the second excitation signal having a second excitation frequency, and wherein the receiving frequency comprises a sum of the first and second excitation frequencies or a difference of the first and second excitation frequencies.

16. The system of claim 10 wherein the first frequency is an excitation frequency and wherein the processor is configured to select the receiving frequency of the receiving oscillating signal from the group consisting of a sub-harmonic, a fundamental frequency, or a harmonic.

17. The system of claim 10 wherein the comparison module is further configured to compare the calculated impedance data to the historical impedance data to determine if a disease is present in the biological sample.

18. A method for analyzing a biological sample contained in a microfluidic unit, the method comprising:

creating an electric field in the microfluidic unit by applying at least one test signal to electrodes of the microfluidic unit, the at least one test signal having a test frequency;

applying a receiving oscillating signal having a receiving frequency to the electrodes;

measuring a voltage signal and a current signal generated in the microfluidic unit as the biological sample passes through the electric field;

multiply the voltage signal and the current signal by the receiving oscillating signal having the receiving frequency to create a plurality of composite signals, the receiving frequency comprising a harmonic of the test frequency;

calculating impedance data of the biological sample as a function of the plurality of composite signals;

retrieving historical impedance data corresponding to the biological sample from a memory;

comparing the calculated impedance data to the historical impedance data to determine a type of the biological sample; and

generating the calculated impedance for display.

19. The method of claim 18 further comprising:

generating the receiving oscillating signal at a second waveform generator; and

multiplying one of the voltage signal and the current signal by the receiving oscillating signal via each of a plurality of mixers to create the plurality of composite signals.

20. The method of claim 19 wherein the receiving oscillating signal comprises a synthesized output component and a phase shifted synthesized output component, and wherein the method further comprises:

multiplying the voltage signal by the synthesized output component at a first mixer to create a first composite signal;

multiplying the current signal by the synthesized output component at a second mixer to create a second composite signal;

multiplying the voltage signal by the phase shifted synthesized output component at a third mixer to create a third composite signal; and

multiplying the current signal by the phase shifted synthesized output component at a fourth mixer to create a fourth composite signal.

21. The method of claim 18 wherein creating the electric field comprises generating a first test signal and a second test signal to apply to the electrodes to create the electric field in the microfluidic unit, the first test signal having a first test frequency and the second test signal having a second test frequency, and wherein the receiving frequency comprises a sum of the first and second test frequencies or a difference of the first and second test frequencies.

22. A multi-channel lock-in amplifier (MCLIA) for analyzing a blood cell comprising:

an electrical interface to connect to electrodes of a microfluidic unit, the microfluidic unit containing the blood cell;

a first waveform generator configured to generate a first excitation signal and a second excitation signal to apply to the electrodes to create an electric field in the microfluidic unit, the first excitation signal having a first excitation frequency and the second excitation signal having a second excitation frequency;

a plurality of lock-in amplifier (LIA) circuits each configured to;

to measure a voltage signal and a current signal generated in the microfluidic unit as the blood cell passes through the electric field; and

to multiply the voltage signal and the current signal by a receiving oscillating signal having a receiving frequency to create a plurality of composite signals, the receiving frequency comprising a sum of the first and second excitation frequencies or a difference of the first and second excitation frequencies; and

a processor comprising modules executable on the processor, the modules comprising;

a detection module configured to detect the connection of the microfluidic unit to the MCLIA to display a menu to a user via a user interface;

a frequency selection module configured to set the excitation frequency in response to input from the user via the user interface;

a mixing frequency selection module configured to set the receiving frequency to the sum of the first and second excitation frequencies or the difference of the first and second excitation frequencies;

a sampling module configured to sample current data and voltage data from the plurality of composite signals;

a data collection module configured to collect the sampled data comprising voltage and current for linear and non-linear responses and to store the sampled voltage and current data in a memory;

a calculation module configured to calculate impedance of the blood cell as a function of the sampled voltage and current data; and

a comparison module configured to compare the calculated impedance to historical linear and non-linear data to determine a type of the blood cell.

23. The MCLIA of claim 22 wherein multiplying the voltage signal and the current signal by the receiving oscillating signal having the receiving frequency enables the detection of a non-linear response from the blood cell.

24. The MCLIA of claim 22 further comprising a histogram module configured to generate a histogram based on the historical linear and non-linear data voltage current data, and wherein the comparison module compares the calculated impedance to historical linear and non-linear data defined by the histogram to determine the type of the blood cell.

25. The MCLIA of claim 22 wherein the comparison module is further configured to compare the calculated impedance data to the historical impedance data to determine if a disease is present in the blood cell.