Dual beam FTIR methods and devices for use in analyte detection in samples of low transmissivity

• US 7,079,252 B1
• Filed: 06/01/2000
• Issued: 07/18/2006
• Est. Priority Date: 06/01/2000
• Status: Expired due to Term

• Current Assignee: Cilag Gmbh International (Johnson & Johnson)
• Original Assignee: Lifescan Incorporated (Duv Holding Corporation)
• Inventors: O'Neil, Michael P., Debreczeny, Martin P.
• Primary Examiner(s): Turner, Samuel A.
• Application Number:
  US09/586,692
• Time in Patent Office: 2,238 Days
• Field of Search: 356/451
• US Class Current: 356/451
• 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: G01J 3/453 by correlation of the amplitudes
• CPC Class Codes: G01J 3/4535 Devices with moving mirror G01J3/4532 takes precedence
• CPC Class Codes: G01N 2021/3595 using FTIR
• CPC Class Codes: G01N 21/35 using infrared light G01N21/39 takes precedence

Abstract

Methods and devices are provided for determining the presence and/or concentration of at least one analyte in a sample of low transmissivity. In the subject methods, a forward beam and a backward beam are produced by or introduced into an interferometer from at least one infrared radiation source. The forward beam is passed into the sample and then collected to produce a sample beam while the backward beam is passed into a reference and then collected to provide a reference beam. The sample and reference beams are recombined either optically into a null beam which is detected at a single detector or electronically nulled after detection on two separate detectors. The presence, and often amount, of at least one analyte in the sample is then derived from the detected null beam. Also provided are devices for practicing the above methods. The subject methods and devices are suitable for use in a variety of different applications, including the detection of the presence, and amount, of one or more blood analytes in a physiological sample, such as blood, tissue or derivatives thereof.

Claims

1. A method of determining the concentration of an analyte in a sample of low transmissivity, said method comprising:

providing a sample of low transmissivity;

producing a sample beam from said sample of low transmissivity and a reference beam from a reference;

producing a null signal from said sample and reference beams; and

deriving the presence of said analyte in said sample of low transmissivity from said null signal.

2. The method according to claim 1, wherein said method comprises using forward and backward beams produced from at least one infrared radiation source to produce said sample and reference beams.

3. The method according to claim 1, wherein said method further comprises passing light through an interferometer.

4. The method according to claim 1, wherein said forward and backward beams are produced from a single infrared radiation source.

5. The method according to claim 1, wherein said forward and backward beams are produced from two infrared radiation sources.

6. A method of determining the concentration of an analyte in a sample of low transmissivity, said method comprising:

providing a sample of low transmissivity;

producing a sample beam from said sample of low transmissivity and a reference beam from a reference using forward and backward beams produced from at least one infrared radiation source;

producing a null signal from said sample and reference beams; and

deriving the presence of said analyte in said sample of low transmissivity from said null signal;

wherein each of said beams pass once through an interferometer.

7. The method according to claim 6, wherein said forward and backward beams are produced from a single infrared radiation source.

8. The method according to claim 6, wherein said forward and backward beams are produced from two infrared radiation sources.

9. The method according to claim 6, wherein said null signal is optically produced by combining said sample and reference beams prior to detection at a single detector.

10. The method according to claim 6, wherein said null signal is electronically produced following detection of said sample and reference beams at two separate detectors.

11. The method according to claim 6, wherein said method further comprises:

producing a forward beam and a backward beam with an interferometer from a single infrared radiation source;

directing said forward beam into said sample of low transmissivity and directing said backward beam into a reference and collecting a sample beam and a reference beam, respectively;

combining said sample and reference beams to produce a nulled beam;

detecting said nulled beam with a single detector to obtain a detected null signal; and

deriving the presence of said analyte in said sample of low transmissivity from said detected null signal.

12. The method according to claim 6, wherein said method further comprises:

producing a forward beam and a backward beam from at least one infrared radiation source;

directing said forward beam through said sample of low transmissivity and directing said backward beam through a reference to produce a sample beam and a reference beam, respectively;

introducing said sample and reference beams into an interferometer and producing a null signal from said sample and reference beams following their exit from said interferometer; and

deriving the presence of said analyte in said sample of low transmissivity from said null signal.

13. The method according to claim 6, wherein said sample of low transmissivity is at least one of highly reflective and highly absorptive.

14. The method according to claim 13, wherein said sample is a physiological sample.

15. The method according to claim 14, wherein said physiological sample is selected from the group consisting of blood, tissue or a derivative thereof.

16. The method according to claim 14, wherein said reference comprises water.

17. The method according to claim 16, wherein said reference is a fluid.

18. The method according to claim 16, wherein said reference is a solid.

19. The method according to claim 6, wherein said reference has a variable pathlength.

20. The method according to claim 6, wherein said analyte is glucose.