Non-invasive substance concentration measurement using and optical bridge

• US 7,003,337 B2
• Filed: 04/26/2002
• Issued: 02/21/2006
• Est. Priority Date: 04/26/2002
• Status: Expired due to Term

• Current Assignee: Grove Instruments, Inc.
• Original Assignee: VivaScan Corp.
• Inventors: Kun, Stevan, Harjunmaa, Hannu, Peura, Robert A., Rolls, John A.
• Primary Examiner(s): WINAKUR, ERIC FRANK
• Application Number:
  US10/134,310
• Publication Number:
  US 20030204133A1
• Time in Patent Office: 1,397 Days
• Field of Search: 600322-326, 600/316, 600/334, 600/335
• US Class Current: 600/316
• CPC Class Codes: A61B 5/14532 for measuring glucose, e.g. by tissue impedance measurement
• CPC Class Codes: A61B 5/1455 using optical sensors, e.g. spectral photometrical oximeters
• CPC Class Codes: G01N 2021/1723 Fluid modulation
• CPC Class Codes: G01N 21/1717 with a modulation of one or more physical properties of the sample during the optical investigation, e.g. electro-reflectance
• CPC Class Codes: G01N 21/3151 using two sources of radiation of different wavelengths G01N21/33 - G01N21/39 take precedence
• CPC Class Codes: G01N 21/35 using infrared light G01N21/39 takes precedence
• CPC Class Codes: G01N 21/49 within a body or fluid

Abstract

An improved method for non-invasively measuring a concentration of a target analyte dissolved in a fluid flowing through a sample is presented. It includes directing a probe beam of electromagnetic radiation, consisting of time multiplexed components of different wavelengths, through the sample and measuring the difference of the absorption of the radiation at at least one wavelength pair at different sample states. During sample state changes, the amount of fluid containing the target analyte within the sample is changing, which varies the total amount of target analyte in the sample, as well as the absorption properties of the sample. The sample states are produced, for instance, by compressing and uncompressing the tissue sample. The accuracy of the presented method is enhanced by including continuous estimation of the amount of the fluid containing the target analyte within the sample, and measurement of the variations of the absorption at a wavelength at which the target analyte absorbs significantly. The method is particularly useful in measuring the concentration of a target analyte, such as glucose, in tissue containing blood. An apparatus for performing this method also is disclosed.

Claims

1. A method of non-invasive measurement of a concentration of a target analyte in a fluid within a sample matrix, the method comprising the steps of:

directing a combined beam of electromagnetic radiation at the sample, the combined beam including at least two repetitive periods of radiation having different wavelengths, the target analyte having different absorption coefficients for two of the different wavelengths, the two wavelengths forming a wavelength pair;

while the sample is at a first sample fluid state having an initial amount of fluid, detecting the combined beam with a sample detector arranged to detect a portion of the radiation transmitted through or reflected by the sample to generate an output signal proportional to the intensity of the combined beam at each of the two repetitive periods of radiation of the wavelength pair;

subjecting the sample to a second sample fluid state to change the amount of fluid within the sample;

measuring the output signal of the sample detector and obtaining an estimate of the amount of fluid in the sample while the amount of fluid in the sample varies from the initial amount in the first fluid state to a second amount in the second fluid state; and

combining the measured output signal from the sample detector with the estimate of the amount of the fluid containing the target analyte to produce an estimate of the concentration of the analyte in the fluid;

wherein during one of the sample fluid states, the detected intensities at each of the at least two repetitive periods of radiation are made substantially equal by adjusting the intensity of at least one of the repetitive periods of radiation entering the sample.

2. The method of claim 1, wherein one of the sample fluid states is chosen to displace the fluid from the sample, and the other sample state is chosen to allow fluid to return to the sample.

3. The method of claim 1,

wherein the sample fluid state alternations are repeated, and the combined beam is detected with the sample detector during each of several cycles of the sample state alternation, where the sample state alternation causes changes in the amount of fluid within the sample.

4. The method of claim 3, wherein two discrete sample fluid states are alternated.

5. The method of claim 3, wherein the sample fluid states are varied between two extreme sample states, wherein in one extreme sample state substantially all fluid is displaced from the sample, and in the other extreme sample state, substantially all of the displaced fluid content is permitted to return to the sample.

6. The method according to claim 1, wherein the sample matrix comprises biologic tissue and the fluid comprises blood.

7. The method according to claim 1, wherein the wavelengths of the wavelength pair have fixed predetermined values.

8. The method according to claim 1, further comprising:

directing a second beam of radiation onto the sample, the second beam of radiation having a wavelength that is preferentially absorbed by a component of the fluid, the component being significantly less abundant in the sample matrix; and

,

at a detector, detecting a portion of the second beam that is transmitted through or reflected by the sample to obtain the estimate of the amount of fluid within the sample.

9. The method according to claim 1, wherein the estimate of the amount of fluid in the sample is obtained using laser Doppler anemometry.

10. The method according to claim 1, wherein the estimate of the amount of fluid in the sample is obtained by measuring the electrical impedance of the sample.

11. The method according to claim 1, wherein the estimate of the amount of fluid in the sample is obtained using ultrasound.

12. The method according to claim 1, wherein the first sample fluid state is obtained by applying a compression pressure to the sample for a time period of approximately 1 to 100 seconds.

13. The method according to claim 12, wherein the second sample fluid state is obtained by uncompressing the sample, and the output signal of the sample detector is measured and the amount of fluid is estimated within a measurement time period of approximately 0.1 to 10 seconds after the sample is uncompressed.

14. The method of claim 13, wherein the difference in sample thickness between the two sample fluid states is a predetermined constant.

15. The method of claim 13, wherein the difference in sample thickness between the two sample fluid states is proportional to the sample thickness at the first sample fluid state.

16. The method of claim 13, wherein the estimate of fluid content is obtained at multiple occasions during the measurement time period.

17. The method of claim 12, wherein at one of the sample fluid states, the sample is compressed with a predetermined constant force.

18. The method according to claim 1, wherein the sample is part of a human earlobe.

19. The method according to claim 1, wherein the sample is skin between fingers or toes of a subject.

20. The method according to claim 1, wherein the sample is part of a tongue of a subject.

21. The method according to claim 1, wherein the sample is part of a lip of a subject.

22. The method according to claim 1, wherein the sample is part of a nose of a subject.

23. The method according to claim 1, wherein the sample is part of the nasal septum of a subject.

24. The method according to claim 1, wherein the sample is part of a cheek of a subject.

25. A method of non-invasive measurement of a concentration of a target analyte in a fluid within a sample matrix, the method comprising the steps of:

directing a combined beam of electromagnetic radiation at the sample, the combined beam including at least two repetitive periods of radiation having different wavelengths, the target analyte having different absorption coefficients for two of the different wavelengths, the two wavelengths forming a wavelength pair;

while the sample is at a first sample fluid state having an initial amount of fluid, detecting the combined beam with a sample detector arranged to detect a portion of the radiation transmitted through or reflected by the sample to generate an output signal proportional to the intensity of the combined beam at each of the two repetitive periods of radiation of the wavelength pair;

subjecting the sample to a second sample fluid state to change the amount of fluid within the sample;

measuring the output signal of the sample detector and obtaining an estimate of the amount of fluid in the sample while the amount of fluid in the sample varies from the initial amount in the first fluid state to a second amount in the second fluid state; and

combining the measured output signal from the sample detector with the estimate of the amount of the fluid containing the target analyte to produce an estimate of the concentration of the analyte in the fluid, wherein the wavelengths of the wavelength pair are selected to minimize the detected transmission or reflection difference between the wavelength periods measured during a sample state.

26. A method of non-invasive measurement of a concentration of a target analyte in a fluid within a sample matrix, the method comprising the steps of:

directing a combined beam of electromagnetic radiation at the sample, the combined beam including at least two repetitive periods of radiation having different wavelengths, the target analyte having different absorption coefficients for two of the different wavelengths, the two wavelengths forming a wavelength pair;

while the sample is at a first sample fluid state having an initial amount of fluid, detecting the combined beam with a sample detector arranged to detect a portion of the radiation transmitted through or reflected by the sample to generate an output signal proportional to the intensity of the combined beam at each of the two repetitive periods of radiation of the wavelength pair;

subjecting the sample to a second sample fluid state to change the amount of fluid within the sample;

measuring the output signal of the sample detector and obtaining an estimate of the amount of fluid in the sample while the amount of fluid in the sample varies from the initial amount in the first fluid state to a second amount in the second fluid state; and

combining the measured output signal from the sample detector with the estimate of the amount of the fluid containing the target analyte to produce an estimate of the concentration of the analyte in the fluid, wherein the intensities of the periods of radiation are adjusted when the sample is at a first sample fluid state, and at least one of the wavelengths of the at least two repetitive periods of radiation is selected to minimize the detected transmission or reflection difference when the sample is at a state different from the first state.

27. The method of claim 26, wherein at the second sample fluid state the amount of fluid within the sample is larger than the amount of fluid in the sample at the first sample state.

28. A method of non-invasive measurement of a concentration of a target analyte in a fluid within a sample matrix, the method comprising the steps of:

directing a combined beam of electromagnetic radiation at the sample, the combined beam including at least two repetitive periods of radiation having different wavelengths, the target analyte having different absorption coefficients for two of the different wavelengths, the two wavelengths forming a wavelength pair;

while the sample is at a first sample fluid state having an initial amount of fluid, detecting the combined beam with a sample detector arranged to detect a portion of the radiation transmitted through or reflected by the sample to generate an output signal proportional to the intensity of the combined beam at each of the two repetitive periods of radiation of the wavelength pair;

subjecting the sample to a second sample fluid state to change the amount of fluid within the sample;

measuring the output signal of the sample detector and obtaining an estimate of the amount of fluid in the sample while the amount of fluid in the sample varies from the initial amount in the first fluid state to a second amount in the second fluid state; and

combining the measured output signal from the sample detector with the estimate of the amount of the fluid containing the target analyte to produce an estimate of the concentration of the analyte in the fluid, wherein the start of a sample fluid state variation is synchronized to a pulsation of the sample fluid.

29. The method of claim 28, wherein there is a variable delay between the phase of the pulsation of the fluid and the start of the sample fluid state change.

30. The method of claim 29, wherein the delay is arranged to promote the largest rate of change of fluid content in the sample between the first and second sample fluid states.

31. The method of claim 28, further comprising:

directing a beam of radiation onto the sample, the beam of radiation having a wavelength that is preferentially absorbed by a component of the fluid, this component being significantly less abundant in the rest of the sample; and

at a detector, detecting a portion of the beam that is transmitted through or reflected by the sample to enable synchronization of the start of a change of the sample fluid state to the pulsation of the fluid.

32. The method of claim 28, wherein the synchronization is obtained using a pulse oximeter.

33. The method according to claim 28, wherein the target analyte is glucose, the fluid containing the target analyte is blood, and the pulsations of the fluid containing the analyte are blood pressure variations due to the pumping action of the heart.

34. The method of claim 33, wherein the wavelength that is strongly absorbed by glucose is substantially in the range of 1550 to 1700 nm, and the wavelength lightly absorbed by glucose is substantially in the range of 1350 to 1430 nm.

35. An apparatus for non-invasively measuring a concentration of a target analyte in a fluid within a sample, comprising:

a source for generating a combined beam of electromagnetic radiation including at least two repetitive periods of radiation having different wavelengths, at least two of the wavelengths having different absorption coefficients for the target analyte;

a mount for positioning a sample within an optical path of the combined beam;

means for controlling the amount of fluid within the sample to maintain a first sample fluid state with an initial amount of fluid within the sample, followed by a second sample fluid state with a second amount of fluid within the sample;

a sample detector arranged to detect a portion of the combined beam transmitted through or reflected by the sample, the sample detector generating an output signal proportional to the detected intensity of the combined beam at each of the two repetitive periods of radiation;

means for obtaining an estimate of the amount of the fluid in the sample while the amount of fluid in the sample varies from the initial amount in the first fluid state to a second amount in the second fluid state;

a processor for controlling the measurement sequence and combining the measured output signal from the sample detector with the estimate of the amount of fluid, to produce an estimate of the concentration of the target analyte in the fluid; and

means for measuring a phase of pulsation of the fluid within the matrix.

36. The apparatus of claim 35, wherein the means for measuring a phase of pulsation comprises:

a source for directing radiation at the sample, the radiation having a wavelength that is preferentially absorbed by a component of the fluid, the component being significantly less abundant in the rest of the sample; and

a detector for monitoring the radiation transmitted through or reflected by the sample.

37. The apparatus of claim 36, wherein the sample comprises body tissue, the fluid comprises blood, the pulsations of the fluid comprise blood pressure variations due to the pumping action of the heart, and the component of the fluid comprises hemoglobin.

38. The apparatus of claim 35, wherein the wavelengths of the at least two repetitive periods of radiation have fixed predetermined values.

39. The apparatus of claim 35 wherein the means for obtaining the estimate of the amount of fluid containing the target analyte comprises:

a source for directing radiation at the sample, the radiation having a wavelength that is preferentially absorbed by a component of the fluid, this component being significantly less abundant in the fixed sample matrix; and

a detector for monitoring the radiation transmitted through or reflected by the sample.

40. The apparatus of claim 35 wherein the means for obtaining an estimate of the amount of the fluid comprises a laser Doppler anemometry flow-meter.

41. The apparatus of claim 35 wherein the means for controlling the amount of the fluid in the sample comprises a compression mechanism for compressing and uncompressing the sample.

42. The apparatus of claim 41, wherein the compression mechanism subjects the sample to the first sample fluid state by compressing the sample with a predetermined constant force.

43. The apparatus of claim 41, wherein the compression mechanism is adapted to compress an earlobe of a human patient.

44. The apparatus of claim 41, wherein the compression mechanism is adapted to compress skin between the fingers or toes of a subject.

45. The apparatus of claim 41, wherein the compression mechanism is adapted to compress a tongue of a subject.

46. The apparatus of claim 41, wherein the compression mechanism is adapted to compress a lip of a subject.

47. The apparatus of claim 41, wherein the compression mechanism is adapted to compress a nose of a subject.

48. The apparatus of claim 41, wherein the compression mechanism is adapted to compress the nasal septum of a subject.

49. The apparatus of claim 41, wherein the compression mechanism is adapted to compress a cheek of a subject.

50. The apparatus of claim 41, wherein the compressing force is provided by an electrical actuator.

51. The method of claim 41, wherein the compression force is provided by a hydraulic actuator.

52. The method of claim 41, wherein the compression force is provided by a pneumatic actuator.

53. The apparatus of claim 35 wherein the source for generating a combined begin comprises an incandescent lamp for generating electromagnetic radiation and an acousto-optical tunable filter for producing a radiation beam of at least two repetitive periods having different wavelengths.

54. The apparatus of claim 35 wherein the source for generating a combined beam comprises of at least one laser source for generating at least two repetitive periods of electromagnetic radiation having different wavelengths.

55. The apparatus of claim 35 wherein the source for generating a combined beam comprises of an incandescent lamp for generating electromagnetic radiation and at least one filter for separating the radiation into at least two repetitive periods having different wavelengths.

56. The apparatus of claim 35 wherein the target analyte is glucose.

57. The apparatus of claim 35 wherein one of the repetitive periods of radiation has a wavelength substantially in the range of 1550 to 1700 nm and another of the repetitive periods of radiation has a wavelength substantially in the range of 1350 and 1430 nm.

58. An apparatus for non-invasively measuring a concentration of a target analyte in a fluid within a sample, comprising:

a source for generating a combined beam of electromagnetic radiation including at least two repetitive periods of radiation having different wavelengths, at least two of the wavelengths having different absorption coefficients for the target analyte;

a mount for positioning a sample within an optical path of the combined beam;

means for controlling the amount of fluid within the sample to maintain a first sample fluid state with an initial amount of fluid within the sample, followed by a second sample fluid state with a second amount of fluid within the sample;

a sample detector arranged to detect a portion of the combined beam transmitted through or reflected by the sample, the sample detector generating an output signal proportional to the detected intensity of the combined beam at each of the two repetitive periods of radiation;

means for obtaining an estimate of the amount of the fluid in the sample while the amount of fluid in the sample varies from the initial amount in the first fluid state to a second amount in the second fluid state;

a processor for controlling the measurement sequence and combining the measured output signal from the sample detector with the estimate of the amount of fluid, to produce an estimate of the concentration of the target analyte in the fluid; and

means for synchronizing the start of a change in sample state to the phase of pulsation of the fluid within the sample.

59. The apparatus of claim 58, wherein the synchronization includes a variable delay between the phase of the pulsation of the fluid and the start of the sample fluid state change.

60. The apparatus of claim 58, wherein the means for synchronizing includes a pulse oximeter.

61. The apparatus of claim 58, wherein the means for synchronizing includes an electrocardiogram detection device.

62. An apparatus for non-invasively measuring a concentration of a target analyte in a fluid within a sample, comprising:

a source for generating a combined beam of electromagnetic radiation including at least two repetitive periods of radiation having different wavelengths, at least two of the wavelengths having different absorption coefficients for the target analyte;

a mount for positioning a sample within an optical path of the combined beam;

means for controlling the amount of fluid within the sample to maintain a first sample fluid state with an initial amount of fluid within the sample, followed by a second sample fluid state with a second amount of fluid within the sample;

a sample detector arranged to detect a portion of the combined beam transmitted through or reflected by the sample, the sample detector generating an output signal proportional to the detected intensity of the combined beam at each of the two repetitive periods of radiation;

means for obtaining an estimate of the amount of the fluid in the sample while the amount of fluid in the sample varies from the initial amount in the first fluid state to a second amount in the second fluid state;

a processor for controlling the measurement sequence and combining the measured output signal from the sample detector with the estimate of the amount of fluid, to produce an estimate of the concentration of the target analyte in the fluid, wherein one of the wavelengths of the at least two repetitive periods of radiation is selected to minimize the intensity of the detected transmission or reflection difference between the wavelength periods in one of the sample states.

63. A system for non-invasive measurement of a concentration of a target analyte in a fluid within a sample matrix, comprising:

an optical bridge measurement device which generates an output signal indicative of the differential optical absorption in the sample between two or more radiation beams having different wavelengths, the target analyte having different absorption coefficients for two of the different wavelengths;

a fluid variation device which varies the amount of fluid within the sample between an initial amount and a second amount;

a fluid content estimation device which generates an output signal indicative of the amount of fluid in the sample; and

a measurement device which records the output of the optical bridge device and the output of the fluid content estimation device multiple times while the amount of fluid varies between the initial amount and the second amount.

64. The system of claim 63, wherein the optical bridge measurement device comprises an incandescent lamp for generating electromagnetic radiation and an acousto-optical tunable filter for producing a radiation beam of at least two repetitive periods having different wavelengths.

65. The system of claim 63, wherein the optical bridge measurement device comprises of at least one laser source for generating at least two repetitive periods of electromagnetic radiation having different wavelengths.

66. The system of claim 63, wherein the optical bridge measurement device comprises of an incandescent lamp for generating electromagnetic radiation and at least one filter for separating the radiation into at least two repetitive periods having different wavelengths.

67. The system of claim 63 wherein the target analyte is glucose.

68. The system of claim 63 wherein one of the radiation beams has a wavelength substantially in the range of 1550 to 1700 nm and another of the radiation beams has a wavelength substantially in the range of 1350 and 1430 nm.

69. The system of claim 63, wherein the fluid content estimation device comprises a source for directing radiation at the sample, the radiation having a wavelength that is preferentially absorbed by a component of the fluid, this component being significantly less abundant in the fixed sample matrix;

and a detector for monitoring the radiation transmitted through or reflected by the sample.

70. A method for non-invasive measurement of a concentration of a target analyte in a fluid within a sample matrix, comprising:

varying the amount of fluid within the sample between an initial amount and a second amount;

recording the output of an optical bridge measurement device multiple times while the amount of fluid varies between the initial amount and the second amount; and

recording an estimate of the fluid content in the sample multiple times while the amount of fluid varies between the initial amount and the second amount.

71. The method of claim 70, wherein the sample matrix comprises biologic tissue and the fluid comprises blood.

72. The method of claim 71, wherein the target analyte comprises glucose.

73. The method of claim 70, wherein the estimate of fluid content is obtained by directing a beam of radiation onto the sample, the beam having a wavelength that is preferentially absorbed by a component of the fluid, the component being significantly less abundant in the sample matrix;

and at a detector, detecting a portion of the second beam that is transmitted through or reflected by the sample to obtain the estimate of the amount of fluid within the sample.

74. The method of claim 70, wherein the initial amount of fluid in the sample is obtained by applying a compression pressure to the sample for a time period of approximately 1 to 100 seconds.

75. The method of claim 74, wherein the second amount of fluid in the sample is obtained by uncompressing the sample, and the output of the optical bridge measurement device is recorded and the estimate of fluid content is recorded over a measurement time period of approximately 0.1 to 10 seconds after the sample is uncompressed.

76. The method of claim 74, wherein the sample comprises tissue from at least one of an earlobe, skin between fingers or toes, a tongue, a lip, a nose, and a cheek.