Methods and devices for non-invasive analyte measurement

• US 8,317,700 B2
• Filed: 04/11/2007
• Issued: 11/27/2012
• Est. Priority Date: 04/11/2006
• Status: Expired due to Fees

• Current Assignee: United States Department of Veterans Affairs (Government of the United States of America), Oregon Health & Science University
• Original Assignee: US Department of Veterans Affairs (Government of the United States of America), Oregon Health & Science University
• Inventors: Jacobs, Peter G., Konrad-Martin, Dawn, Wan, Eric
• Primary Examiner(s): Natnithithadha, Navin
• Application Number:
  US12/294,558
• Publication Number:
  US 20090306490A1
• Time in Patent Office: 2,057 Days
• Field of Search: 600/365, 600/300, 600/361
• US Class Current: 600/365
• CPC Class Codes: A61B 5/14532 for measuring glucose, e.g. by tissue impedance measurement
• CPC Class Codes: A61B 5/4052 efferent nerves, i.e. nerves that relay impulses from the central nervous system
• CPC Class Codes: A61B 5/6817 Ear canal
• CPC Class Codes: A61B 7/00 Instruments for auscultation

Abstract

Methods and compositions for the non-invasive determination of the concentration of an analyte are provided.

Claims

1. A system for determining a concentration of at least one analyte in a subject comprising:

a) means for producing and recording at least one pressure signal;

b) means for producing an audio signal to the ear of said subject, wherein application of the audio signal evokes a measured pressure signal in the ear of said patient; and

c) at least one computing device to handle data acquisition, wherein said computing device comprises means for converting measured pressure signal information to an output of the concentration of said at least one analyte in said subject.

2. The system of claim 1 which is contained within a hand-held device or headphones.

3. The system of claim 1, wherein said means for converting the measured pressure signal comprises applying an algorithm correlating a characteristic of said measured pressure signal with said analyte concentration.

4. The system of claim 1 further comprising means for amplifying the pressure stimuli.

5. The system of claim 1 further comprising means for filtering the pressure stimuli.

6. The system of claim 1 further comprising a visual display for displaying the concentration of the at least one analyte.

7. The system of claim 1 further comprising a means for providing a physical print out of the concentration of the at least one analyte.

8. The system of claim 1 further comprising a means of transmitting the concentration of the at least one analyte to a computer.

9. A method for determining the concentration of at least one analyte in a patient comprising:

a) evoking a measured pressure signal in the ear of said patient by applying an audio signal to said ear;

b) measuring at least one characteristic of said measured pressure signal; and

c) applying an algorithm correlating said characteristic of said measured pressure signal with said analyte concentration to the measured characteristic of step b), thereby determining said concentration of at least one analyte in said patient.

10. The method of claim 9, wherein said analyte is associated with a disease or disorder.

11. The method of claim 10, wherein said analyte is glucose.

12. The method of claim 9, wherein said measured pressure signal is an otoacoustic emission (OAE).

13. The method of claim 9, wherein said measured pressure signal represents a measure of the middle ear muscle reflex.

14. The method of claim 9, wherein said audio signal consists of at least one waveform selected from the group consisting of a constant, stepped, ramped, periodic, tone, chirp, click and noise.

15. The method of claim 9, wherein said measured pressure signal is masked by at least one stimulus pressure signal selected from the group consisting of a constant, stepped, ramped, periodic, tone, chirp, click and noise.

16. The method of claim 15, wherein said masking stimulus pressure signal is provided contralaterally, ipsilaterally, or both.

17. The method of claim 15, wherein said masked measured pressure signal represents a measure of at least one of the reflexes selected from the group consisting of the medial olivococlear reflex, the lateral olivocochlear reflex, and the middle ear muscle reflex.

18. The method of claim 9, wherein said characteristic of said measured pressure signal is selected from the group consisting of amplitude, latency, signal-to-noise ratio, rise time, fall time, frequency, phase, and duration.

19. The method of claim 9, wherein step c) comprises using a computing device having means for converting measured pressure signal information to an output of the concentration of said at least one analyte in said subject.