Method And Apparatus For Determining Marker Gas Concentration Using An Internal Calibrating Gas

• US 20070081162A1
• Filed: 12/14/2006
• Published: 04/12/2007
• Est. Priority Date: 01/11/2002
• Status: Abandoned Application

• Current Assignee: Ekips Technologies, Inc.
• Original Assignee: Ekips Technologies, Inc.
• Inventors: Jeffers, James, Namjou, Khosrow, Roller, Chad
• Application Number:
  US11/610,997
• Publication Number:
  US 20070081162A1
• Time in Patent Office: Days
• US Class Current: 356/437
• CPC Class Codes: A61B 5/0075 by spectroscopy, i.e. measuring spectra, e.g. Raman spectroscopy, infrared absorption spectroscopy A61B5/0071 takes precedence
• CPC Class Codes: A61B 5/082 Evaluation by breath analysis, e.g. determination of the chemical composition of exhaled breath A61B5/083, A61B5/091 take precedence
• CPC Class Codes: G01N 2021/399 Diode laser
• CPC Class Codes: G01N 21/031 Multipass arrangements
• CPC Class Codes: G01N 21/274 Calibration, base line adjustment, drift correction
• CPC Class Codes: G01N 21/3504 for analysing gases, e.g. multi-gas analysis
• CPC Class Codes: G01N 33/0037 NOx
• CPC Class Codes: G01N 33/497 of gaseous biological material, e.g. breath
• CPC Class Codes: Y02A 50/20 Air quality improvement or preservation, e.g. vehicle emission control or emission reduction by using catalytic converters

Abstract

A method and an apparatus for measuring the concentration of a specific gas component of a gas mixture including another gas whose concentration is independently known using light absorption spectroscopy are provided. A method and an apparatus for assessing human airway inflammation by measuring the concentration of exhaled NO and CO₂ present in orally exhaled breath using light absorption spectroscopy are also provided. NO concentration is determined at the time during breath sampling corresponding to a known exhaled CO₂ concentration. Methods and apparatus are further provided for measuring NO concentration in orally exhaled human breath that analyze breath emanating from the lower airways and lungs, while excluding breath from the nasal cavity. They include steps and apparatus for discarding initially exhaled breath, flowing breath through an analysis chamber using a vacuum pump and flowing breath through an analysis chamber using a vacuum pump at an initial flow rate and later at a flow rate higher than the initial flow rate.

Claims

1. A spectrometer system for measuring the concentration of a marker gas in a gas mixture, the system comprising:

a spectrometer gas sample cell;

a spectrometer light source adapted to pass a light beam through the gas sample cell;

a spectrometer detector adapted to produce a signal sampling characteristic of the gas mixture in response to light passing through the gas mixture; and

a spectrometer computer adapted to acquire the signal sampling from the spectrometer detector over a signal acquisition interval and generate a gas mixture spectrum;

wherein the spectrometer computer is further adapted to analyze the gas mixture spectrum to determine a marker gas absorption intensity and a calibration gas absorption intensity as a function of time over a plurality of signal acquisition intervals to identify a signal acquisition interval where a known concentration calibration gas absorption intensity corresponds to an independently known calibration gas concentration and a simultaneous marker gas absorption; and

to calculate a ratio of the simultaneous marker gas absorption intensity to the known concentration calibration gas absorption intensity and multiplying the ratio by a proportionality constant to determine concentration of the marker gas.

2. The system of claim 1 wherein the gas mixture sample comprises exhaled breath.

3. The system of claim 1 wherein the spectrometer gas sample cell has a pressure selected to reduce line broadening and interference between the marker gas absorption intensity and the calibration gas absorption intensity.

4. The system of claim 2 wherein the marker gas is characteristic of a disease.

5. The system of claim 1 wherein the marker gas comprises NO.

6. The system of claim 1 wherein the marker gas comprises H₂S.

7. The system of claim 1 wherein the marker gas comprises OCS.

8. The system of claim 1 wherein the calibration gas comprises CO₂.

9. The system of claim 1 wherein the calibration gas comprises H₂O.

10. The system of claim 1 wherein the spectrometer light source comprises a mid-infrared tunable laser.

11. The system of claim 1 wherein the spectrometer light source comprises an IV-VI diode laser.

12. The system of claim 11 wherein the IV-VI diode laser comprises an emission wavelength in the range of from about 3 μ

m to about 10 μ

m.

13. The system of claim 1 wherein the spectrometer gas sample cell comprises a Herriott cell.

14. The system of claim 1 wherein the spectrometer gas sample cell comprises a multi-pass White cell.

15. The system of claim 1 wherein the gas mixture spectrum generated by the spectrometer computer is a second harmonic absorption spectrum.

16. The system of claim 1 wherein the spectrometer computer is further adapted to calculate a running co-average of a plurality of signal samplings to obtain co-averaged signal samplings, and to digitally filter the co-averaged signal samplings to generate the gas mixture spectrum.

17. A method for comparing a concentration of a marker gas to a concentration of a calibration gas, wherein the calibration gas and marker gas are intrinsic in a gas sample and wherein the calibration gas has an independently known concentration, the method comprising:

placing the gas mixture sample in a spectrometer gas sample cell over a sampling interval;

illuminating the gas mixture sample within the spectrometer gas sample cell over the sampling interval to generate a signal sampling characteristic of the gas mixture sample;

generating a plurality of gas mixture spectra;

analyzing the gas mixture spectra to measure a marker gas intensity and a calibration gas intensity for each of the plurality of spectra as a function of time over the sampling interval to identify a single spectrum wherein a known concentration calibration gas intensity corresponds to an independently known calibration gas concentration and a simultaneous marker gas intensity; and

calculating a ratio of the simultaneous marker gas intensity to the known concentration calibration gas intensity and multiplying the ratio by a proportionality constant to determine concentration of the marker gas.

18. The method of claim 17 wherein said gas mixture sample comprises exhaled breath.

19. The method of claim 17 further comprising maintaining the spectrometer gas sample cell at a pressure selected to reduce line broadening and interference.

20. The method of claim 18 wherein the marker gas is characteristic of a disease.

21. The method of claim 20 wherein the marker gas comprises CH₃O.

22. The method of claim 20 wherein the marker gas comprises H₂S.

23. The method of claim 20 wherein the marker gas comprises OCS.

24. The method of claim 17 wherein the calibration gas comprises CO₂.

25. The method of claim 17 wherein the calibration gas comprises H₂O.

26. The method of claim 17 wherein illuminating the gas mixture sample comprises passing a mid-infrared tunable laser beam through the gas mixture sample.

27. The method of claim 26 wherein laser beam comprises an emission wavelength in the range from about 3 μ

m to about 10 μ

m.

28. The method of claim 17 wherein the spectrometer gas sample cell comprises a Herriott cell.

29. The method of claim 17 wherein the spectrometer gas sample cell comprises a multi-pass White cell.

30. The method of claim 17 wherein the gas mixture spectra comprise second harmonic spectra.

31. The method of claim 17 further comprising calculating a running co-average of the marker gas intensities and the calibration gas intensities over the sampling interval.