NONINVASIVE MEASUREMENT OF ANALYTE CONCENTRATION USING METHODS AND SYSTEMS OF POST-BALANCING

• US 20160206231A1
• Filed: 01/21/2015
• Published: 07/21/2016
• Est. Priority Date: 01/21/2015
• Status: Abandoned Application

• Current Assignee: Grove Instruments, Inc.
• Original Assignee: Grove Instruments, Inc.
• Inventors: Kun, Stevan, Harjunmaa, Hannu, Burrell, Rebecca
• Application Number:
  US14/601,395
• Publication Number:
  US 20160206231A1
• Time in Patent Office: Days
• US Class Current: 1/1
• CPC Class Codes: A61B 2562/0238 Optical sensor arrangements for performing transmission measurements on body tissue
• CPC Class Codes: A61B 5/02422 within occluders
• CPC Class Codes: A61B 5/14532 for measuring glucose, e.g. by tissue impedance measurement
• CPC Class Codes: A61B 5/14546 for measuring analytes not otherwise provided for, e.g. ions, cytochromes
• CPC Class Codes: A61B 5/14552 Details of sensors specially adapted therefor
• CPC Class Codes: A61B 5/7246 using correlation, e.g. template matching or determination of similarity

Abstract

A noninvasive method for estimating a concentration of a target analyte in a sample comprises generating a first and second (reference) radiation, a principal radiation and a target analyte carrier detection radiation; directing the first, second, principal and the target analyte carrier detection radiations at the sample which includes the target analyte; and detecting a first, second, principal and target analyte carrier detection amount of the radiation that leaves the sample. The method further comprises modulating the sample thickness in order to achieve time-wise or spatial target analyte concentration variation within the sample. The method further comprises generating first, second, principal and target analyte carrier detection measurement data based respectively on the first, second, the principal and the target analyte carrier detected amounts of radiation; numerically processing the first, second, principal and target analyte carrier detection measurement data to obtain a weighted combination of the first measurement data and the second measurement data that balances the principal measurement data with respect to a sample background; and estimating the concentration of the target analyte based on the difference between the balanced weighted combination of the first measurement data and the second measurement data vs. the principal measurement data.

Claims

1. A noninvasive method for estimating a concentration of a target analyte in a sample, comprising:

generating a first reference radiation having a first reference wavelength, a second reference radiation having a second reference wavelength, a principal radiation having a principal wavelength, and a target analyte carrier detection radiation having the target analyte carrier detection wavelength, using a first reference light source, a second reference light source, a principal light source, and a target analyte carrier detection light source, respectively;

directing the first reference radiation, the second reference radiation, the principal radiation and the target analyte carrier detection radiation at the sample which includes the target analyte;

detecting, with one or more detectors, a first amount of the first reference radiation, a second amount of the second reference radiation, a third amount of the principal radiation, and a fourth amount of the target analyte carrier detection radiation, that leaves the sample;

causing or permitting modulation of the content of the target analyte in the sample;

generating first reference measurement data, second reference measurement data, principal measurement data, and target analyte carrier detection measurement data, based respectively on the first amount, the second amount, the third amount, and the fourth amount of radiation that are detected;

calculating balancing weights for calculating a weighted combination of the first reference measurement data and the second reference measurement data that balances the principal measurement data with respect to a sample background from the first reference measurement data, the second reference measurement data, the principal measurement data, and the target analyte carrier detection data using one or more processors; and

estimating the concentration of the target analyte based on the difference between the balanced weighted combination of the first reference measurement data and the second reference measurement data and the principal measurement data, and the target analyte carrier detection data.

2. The method of claim 1, wherein:

the first reference radiation, the second reference radiation, the principal radiation, and the target analyte carrier detection radiation are directed at the sample in a repeating, time-multiplexed sequence.

3. The method of claim 1, wherein:

the sample is adjusted to a plurality of thicknesses while the first reference radiation, the second reference radiation, the principal radiation, and the target analyte carrier radiation are directed at the sample and the first amount, the second amount, the principal amount, and the target analyte carrier amount are detected.

4. The method of claim 3, wherein the target analyte is blood glucose and the target analyte carrier is blood.

5. The method of claim 1, wherein:

the first amount, the second amount, the third amount and the fourth amount of radiation that leave the sample are portions of the first reference radiation, the second reference radiation, the principal radiation and the target analyte carrier detection radiation that are transmitted through the sample.

6. The method of claim 1, wherein:

the first amount, the second amount, the third amount and the fourth amount of radiation that leave the sample are portions of the first reference radiation, the second reference radiation, the principal radiation, and the target analyte carrier detection radiation that are transflected by the sample.

7. The method of claim 1, wherein:

the step of calculating balancing weights involves determining the relative balancing weights of the first reference radiation and the second reference radiation that are needed to produce a weighted combination of the first reference measurement data and the second reference measurement data with the principal measurement data, in such a manner that such combination data levels are not influenced by the variations of the thicknesses of those compartments of the sample that do not contain the target analyte or the target analyte carrier.

8. The method of claim 7, comprising:

balancing an Optical Bridge, using measurement data detected from a sample that is made up of mostly background material, with only minimal amounts of target analyte carrier and target analyte.

9. The method of claim 7, further comprising:

balancing an Optical Bridge, using the first reference measurement data, the second reference measurement data, the principal measurement data and the target analyte carrier detection measurement data, detected from a sample that has varying amounts of background material, target analyte and target analyte carrier.

10. The method of claim 8, wherein:

the relative preliminary balancing weights are determined by;

comparing an amount of the first reference radiation that leaves the sample when in a first state with an amount of the first reference radiation that leaves the sample in a second state to determine a first reference attenuation coefficient of the sample background at the first reference wavelength;

comparing an amount of the second reference radiation that leaves the sample when in a first state with an amount of the second reference radiation that leaves the sample in a second state to determine a second reference attenuation coefficient of the sample background at the second reference wavelength;

comparing an amount of the principal radiation that leaves the sample when in a first state with an amount of the principal radiation that leaves the sample in a second state to determine a principal attenuation coefficient of the sample background at the principal wavelength; and

determining the relative preliminary balancing weights at which to combine the first reference attenuation coefficient of the sample background and the second reference attenuation coefficient of the sample background so that their combination equals the principal attenuation coefficient of the sample background.

11. The method of claim 10, wherein:

the first state and the second state correspond to different sample thicknesses.

12. The method of claim 10, wherein:

the first state corresponds to a thickness of the sample when minimal amount of target analyte is present in the sample; and

the second state corresponds to a different thickness of the sample when also minimal amount of target analyte is present in the sample.

13. The method of claim 11, wherein:

the first states of the sample for determining the first reference attenuation coefficient, the second reference attenuation coefficient and the principal attenuation coefficient respectively correspond to sample thicknesses that are substantially the same; and

the second states of the sample for determining the first reference attenuation coefficient, the second reference attenuation coefficient, and the principal attenuation coefficient respectively correspond to sample thicknesses that are substantially the same.

14. The method of claim 11, wherein:

the first state of the sample for determining the first reference attenuation coefficient, the second reference attenuation coefficient, and the principal attenuation coefficient respectively correspond to thicknesses of the sample that are different; and

the second states of the sample for determining the first reference attenuation coefficient, the second reference attenuation coefficient, and the principal attenuation coefficient, respectively correspond to thicknesses of the sample that are different.

15. The method of claim 11, wherein:

the sample thicknesses that correspond to the states of the sample are dynamically chosen during the measurement, based on the first amount, the second amount, the third amount, the fourth amount of radiation that leaves the sample and the pressure measured on the sample.

16. The method of claim 1, wherein:

the first reference light source and the second reference light source are throughout the whole measurement operated, in a pulsed or continuous mode, at constant operation regions that correspond to the best light source stability and least amount of optical noise.

17. The method of claim 1, further comprising:

multiple iterations of processing the first reference measurement data, the second reference measurement data, the principal measurement data, and the target analyte detection measurement data, to improve on the accuracy of the calculated relative preliminary balancing weights and to produce the relative balancing weights that are best representative of the sample background.

18. The method of claim 10, further comprising:

an Unsqueeze Segment during which the thickness of the sample is monotonously increased;

an Isopachic Segment, during which the thickness of the sample is held constant; and

,

a SawTooth segment, during which the thickness of the sample is being varied in a predetermined manner.

19. The method of claim 9, wherein:

the relative balancing weights are determined by;

calculating the first reference sawtooth slope, defined as the first reference measurement data variation vs. sample thickness variation on the measurement segment on which the sample thickness is varied in a predetermined way;

calculating the second reference sawtooth slope, defined as the second reference measurement data variation vs. sample thickness variation on the measurement segment on which the sample thickness is varied in a predetermined way;

calculating the principal sawtooth slope, defined as the principal measurement data variation vs. sample thickness variation on the measurement segment on which the sample thickness is varied in a predetermined way;

calculating the green sawtooth slope, defined as the target analyte carrier detection measurement data variation vs. sample thickness variation on the measurement segment on which the sample thickness is varied in a predetermined way;

calculating the first reference slope, defined as the first reference measurement data variation vs. target analyte carrier detection measurement data variation on the measurement segment on which the sample thickness is constant;

calculating the second reference slope, defined as the second reference measurement data variation vs. target analyte carrier detection measurement data variation on the measurement segment on which the sample thickness is constant;

calculating the principal slope, defined as the principal measurement data variation vs. target analyte carrier detection measurement data variation on the measurement segment on which the sample thickness is constant;

determining a first reference attenuation coefficient of the sample background at the first reference wavelength based on the first reference sawtooth slope, the green sawtooth slope and the first reference slope;

determining a second reference attenuation coefficient of the sample background at the second reference wavelength based on the second reference sawtooth slope, the green sawtooth slope and the second reference slope;

determining a principal attenuation coefficient of the sample background at the principal wavelength based on the principal sawtooth slope, the green sawtooth slope and the principal slope;

determining the relative balancing weights at which to combine the first reference attenuation coefficient of the sample background and the second reference attenuation coefficient of the sample background so that their combination equals the principal attenuation coefficient of the sample background, based on the first reference attenuation coefficient, the second reference attenuation coefficient and the principal attenuation coefficient.

20. The method of claim 3, wherein the target analyte is interstitial glucose and the target analyte carrier is interstitial fluid.

21. The method of claim 3, wherein the target analyte is a blood analyte and the target analyte carrier is blood.

22. The method of claim 3, wherein the target analyte is an interstitial analyte and the target analyte carrier is interstitial fluid.

23. An apparatus for performing noninvasive estimation of a concentration of a target analyte in a sample, comprising:

a first reference light source for generating a first reference radiation;

a second reference light source for generating a second reference radiation;

a principal light source for generating a principal radiation;

a target analyte carrier detection light source for generating a target analyte carrier detection radiation;

a device for altering the content of target analyte, target analyte carrier and sample background material within the sample;

one or more detectors for detecting non-optical sample parameters selected from the group consisting of sample thickness;

pressure on the sample and temperature;

one or more detectors for detecting the first reference radiation, the second reference radiation, the principal radiation and the target analyte carrier detection radiation and generating the corresponding first measurement data, second measurement data, principal measurement data, and target analyte carrier detection data; and

a controller configured to estimate the concentration of the target analyte by;

processing the first measurement data, second measurement data, principal measurement data, and target analyte carrier detection data, using one or more processors, to obtain the first reference attenuation coefficient, the second reference attenuation coefficient, the principal attenuation coefficient, and the target analyte carrier attenuation coefficient of the sample background;

processing the obtained first reference, second reference, principal, and target analyte carrier sample background attenuation coefficients to find the balancing weights needed to generate a weighted combination of the first reference measurement data and the second reference measurement data that balances the principal measurement data with respect to a sample background; and

,

estimating the concentration of the target analyte based on the difference between the balanced weighted combination of the first reference measurement data and the second reference measurement data vs. the principal measurement data.

24. The apparatus of claim 23, wherein:

the controller is configured to operate the first reference light source, the second reference light source, the principal fight source and the target analyte carrier detection light source to generate a repeating, time-multiplexed sequence of the first reference radiation, the second reference radiation, the principal radiation and the target analyte carrier detection radiation.

25. The apparatus of claim 23, wherein:

the controller is configured to control the device which alters the content of the target analyte, target analyte carrier and sample background material within the sample.

26. The apparatus of claim 23, wherein the target analyte is blood glucose and the target analyte carrier is blood.

27. The apparatus of claim 23, wherein the target analyte is interstitial glucose and the target analyte carrier is interstitial fluid.

28. The apparatus of claim 23, wherein the target analyte is a blood analyte and the target analyte carrier is blood.

29. The apparatus of claim 23, wherein the target analyte is an interstitial analyte and the target analyte carrier is interstitial fluid.

30. The apparatus of claim 23, wherein the measurements are performed on the target analyte carrier that is temporarily or permanently removed from the sample.