Spectroscopic analysis of a biological fluid reacted with an enzyme

• US 20060292650A1
• Filed: 05/23/2006
• Published: 12/28/2006
• Est. Priority Date: 05/23/2005
• Status: Abandoned Application

• Current Assignee: OptiScan Biomedical Corporation
• Original Assignee: OptiScan Biomedical Corporation
• Inventors: Sheill, Jane J., Magarian, Margaret, Braig, James R., Sterling, Bernhard B., Witte, Kenneth G.
• Application Number:
  US11/438,902
• Publication Number:
  US 20060292650A1
• Time in Patent Office: Days
• US Class Current: 435/14
• CPC Class Codes: C12Q 1/26 involving oxidoreductase
• CPC Class Codes: C12Q 1/32 involving dehydrogenase
• CPC Class Codes: C12Q 1/52 involving transaminase
• CPC Class Codes: C12Q 1/54 involving glucose or galactose

Abstract

An apparatus is presented for estimating the concentration of an analyte using a combined enzyme-spectroscopic method. Examples are provided for the detection of glucose and lactate. A sample of biological fluid is mixed or contacted with an enzyme specific to the analyte of interest, and the reacting fluid is probed with an optical system at wavelengths that includes at least one wavelength that is sensitive to the analyte concentration and at least one wavelength that is not sensitive to the analyte concentration. The optical system measures properties, such as optical density, and relates the measurements to concentration through a calibration of the system. A method is also provided for analyzing the data obtained from optical measurements of reactions of enzymes with biological fluids. These technologies may be applied to continuous or periodic patient sampling systems or to test strip type devices.

Claims

1. A method for measuring the presence of an analyte in a sample, said method comprising:

reacting the sample with an enzyme that is reactive with the analyte;

measuring a reacting sample spectrum, where said reacting sample spectrum is a infrared absorption spectrum of the sample during said reacting; and

determining the concentration of the analyte in the sample from said reacting sample spectrum.

2. The method of claim 1, where said measuring said reacting sample spectrum includes measuring before completion the reaction of said enzyme and said analyte.

3. The method of claim 1, where said measuring said reacting sample spectrum includes measuring after completion the reaction of said enzyme and said analyte.

4. The method of claim 1, where said measuring is at two or more wavelengths and where said determining includes applying a calibration relating the analyte concentration to said reacting sample spectrum at said two or more wavelengths.

5. The method of claim 4, where said calibration relates a linear combination of the reacting sample spectrum at said two or more wavelengths.

6. The method of claim 4, where said calibration relates a ratio of the reacting sample spectrum said at two or more wavelengths.

7. The method of claim 1, further comprising:

determining an unreacted sample spectrum, where said determining the concentration includes determining the concentration of the analyte in the sample from said unreacted sample spectrum.

8. The method of claim 7, where said determining an unreacted sample spectrum includes measuring the sample spectrum prior to said reacting.

9. The method of claim 7, where said determining an unreacted sample spectrum includes extrapolating said reacting sample spectrum to a zero reaction time.

10. The method of claim 1, further comprising:

obtaining a blood sample from a patient.

11. The method of claim 10, where said obtaining automatically obtains said blood sample from a patient-connected catheter.

12. The method of claim 10, where said enzyme is on a test strip, and where said obtaining includes obtaining blood from a pin prick.

13. The method of claim 1, where said analyte is glucose, and where said enzyme is glucose oxidase or glucose dehydrogenase.

14. The method of claim 1, where said analyte is lactate, and where said enzyme is lactate dehydrogenase, hydroxybutyrate dehydrogenase, or alanine transaminase.

15. The method of claim 1, where said reacting includes:

reacting the sample by contacting the sample with an immobilized enzyme.

16. The method of claim 1, where said reacting includes:

reacting the sample by admixing the sample with an enzyme solution.

17. The method of claim 7, where said determining said unreacted sample spectrum includes:

measuring said reacting sample spectrum at two or more times during said reacting, and

said determining said concentration includes extrapolating said reacting sample spectrum at two or more times during said reacting to an initial reaction time.

18. The method of claim 1, where said measuring said reacting sample spectrum includes measuring said reacting sample spectrum at a fixed time and at two or more wavelengths.

19. The method of claim 18, where said determining includes comparing a linear combination of said spectrum at said two or more wavelengths to a calibration of the concentration as function of said linear combination.

20. The method of claim 1, where said sample is a biological fluid sample and where said analyte is a constituent of said biological fluid sample.

21. The method of claim 20, where said analyte is glucose.

22. An apparatus for accepting a material sample having an initial analyte concentration comprising:

an enzyme for reacting with the accepted material sample;

an optical system to measure an optical property of the reacting material sample at at least two wavelengths; and

a processor programmed to determine the initial analyte concentration from the measured optical properties.

23. The apparatus of claim 22, further comprising a passageway having a surface comprising an immobilized enzyme.

24. The apparatus of claim 22, where said enzyme is in solution, and further comprising a mixing chamber for admixing said enzyme and said accepted material sample.

25. The apparatus of claim 22, where said optical system measures the optical density of the material sample at two or more wavelengths.

26. The apparatus of claim 25, where said two or more wavelengths is two wavelengths.

27. The apparatus of claim 25, where said optical system measures at one or more predetermined times.

28. The apparatus of claim 22, where said analyte is glucose, and where said enzyme is glucose oxidase or glucose dehydrogenase.

29. The apparatus of claim 22, where said analyte is lactate, and where said enzyme is lactate dehydrogenase, hydroxybutyrate dehydrogenase, or alanine transaminase.

30. The apparatus of claim 22, further comprising a test strip, where said enzyme is an immobilized enzyme is on said test strip, and where said test strip is insertable into said optical system.