Method, apparatus and solution for calibration of partial pressure value

• US 5,061,631 A
• Filed: 10/14/1988
• Issued: 10/29/1991
• Est. Priority Date: 10/14/1988
• Status: Expired due to Fees

• Current Assignee: Il Holding SpA (Werfen SA)
• Original Assignee: Fisher Scientific Co. (Thermo Fisher Scientific Incorporated)
• Inventors: Calabrese, Gary S.
• Primary Examiner(s): Lacey, David L.
• Assistant Examiner(s): Chan, William K. Y.
• Application Number:
  US07/257,553
• Time in Patent Office: 1,110 Days
• Field of Search: 422/68.1, 422/81, 422/82.01, 436/11, 436/16, 436/68, 436/50, 252/608.1, 73/1 R
• US Class Current: 436/11
• CPC Class Codes: G01N 27/4163 checking the operation of, or calibrating, the measuring apparatus G01N27/3274, G01N27/4175 and G01N33/0006 take precedence
• CPC Class Codes: Y10T 436/102499 Blood gas standard or control

Abstract

Electrodes for the measurement of pCO2 and/or pO2 are calibrated with an exposed aliquot of a calibration liquid. A constituent such as a ferrioxalate salt in the calibration liquid is converted to the gas in a reproducible concentration by exposure of the aliquot to light. In some instances, the calibration liquid is equilibrated with air prior to exposure. Some mechanisms of light generation of carbon dioxide also consume oxygen, so as to depress the pO2 value by a reproducible amount. The use of two different calibration liquids enables both one-point and two-point calibration of the Clark oxygen electrode and the Severinghaus pCO2 electrode of a blood gas instrument.

Claims

1. A method for the measurement of the partial pressure of a gas in a liquid sample which comprises the steps:

a) providing a calibration liquid having a defined concentration of a dissolved precursor of a gas, the liquid having a composition such that, upon exposure to light, the dissolved precursor reacts to form the gas;

b) exposing an aliquot of the calibration liquid in an exposing means to light of sufficient wavelength, intensity and duration to convert the precursor substantially completely to the gas;

c) conveying the exposed aliquot with the converted precursor to a measuring chamber for contact with a measuring element for the partial pressure of the gas;

d) making a measurement with the measuring element on the exposed aliquot with the converted precursor;

e) conveying the exposed aliquot with the converted precursor away from the measuring element and conveying a liquid sample having an analyte value of the partial pressure of the gas into the measuring chamber in contact with the measuring element;

f) making a measurement with the measuring element on the liquid sample; and

g) comparing the measurement made with the measuring element on the liquid sample to the measurement made with the measuring element on the exposed aliquot of calibration liquid.

2. The method of claim 1 wherein the measuring element is a carbon dioxide electrode.

3. The method of claim 2 wherein the calibration liquid contains a dissolved carbon dioxide precursor which is a photoreactive complex anion of a metal and an carboxlic acid.

4. The method of claim 3 wherein the dissolved carbon dioxide precursor is ferrioxlate anion.

5. The method of claim 4 further comprising equilibrating the aliquot of calibration liquid with air prior to exposing the aliquot in the exposing means.

6. The method of claim 4 wherein the calibration liquid has a pH of 0 to 5, contains at least 0.3 millimoles per liter of oxalate, contains 0.1 to 200 millimoles per liter of iron(III) and has a molar ratio of iron(III) to oxalate of 100:

1 to 1;

7200, provided that when the iron(III) concentration is greater than 5 millimoles per liter, then the oxalate concentration is not greater than 15 millimoles per liter.

7. The method of claim 6 wherein the calibration liquid has a pH of 0 to 2.

8. The method of claim 7 wherein the calibration liquid has a molar ratio of iron(III) to oxalate of 2:

1 to 1;

7200.

9. The method of claim 7 wherein the calibration liquid has a molar ratio of iron(III) to oxalate of 5:

1 to 100;

1.

10. The method of claim 2 wherein the dissolved carbon dioxide precursor is uranyloxalate.

11. The method of claim 1 further comprising equilibrating the aliquot of calibration liquid with air prior to exposing the aliquot in the exposing means.

12. The method of claim 1 wherein the sample liquid is conveyed into the measuring chamber along a first pathway that also brings the sample into contact with a pH electrode and wherein the exposed aliquot of calibration liquid is conveyed into the measuring chamber along a second pathway that does not bring the exposed aliquot into contact with the pH electrode.

13. An apparatus for measuring the partial pressure of a gas in a liquid sample which comprises:

a) exposure means for exposing an aliquot of a calibration liquid to light;

b) a measuring chamber;

c) first conveying means for conveying an exposed aliquot of calibration liquid from the exposure means to the measuring chamber;

d) a measuring means in operative contact with the measuring chamber;

e) second conveying means for conveying a liquid sample into the measuring chamber; and

f) comparator means for comparing the measurement made by the measuring element on the liquid sample with the measurement made by the measuring element on the exposed aliquot of calibration liquid.

14. The apparatus of claim 13 wherein the second conveying means is constructed so as to convey sample along a first pathway that brings liquid sample into the measuring chamber, wherein said measuring means comprises a pCO2 electrode and a pH electrode, and wherein the first conveying means is constructed so as to convey exposed calibration liquid into the measuring chamber without bringing exposed calibration liquid into contact with the pH electrode.

15. The apparatus of claim 13 further comprising tonometry means for equilibrating the aliquot of calibration liquid with air prior to exposing the aliquot of calibration liquid to light in the exposure means.

16. The apparatus of claim 13 further comprising two reservoirs of calibration liquid, and wherein the tonometry means, exposure means and first conveying means are operative to equilibrate, expose and convey into the measuring chamber either an aliquot of calibration liquid in the first reservoir or an aliquot of calibration liquid in the second reservoir.

17. A method for the measurement of the partial pressure of oxygen and carbon dioxide in a liquid sample which comprises the steps:

a) providing first and second calibration liquids comprising aqueous ferrioxalate solutions;

1) the first calibration liquid having a pH of 0 to 2, an oxalate concentration of 0.6 to 1.5 millimoles per liter, a molar ratio of iron(III) to oxalate of 5;

1 to 100;

1 and an iron concentration of 3 to 150 millimoles per liter; and

2) the second calibration liquid having a pH of 0 to 2, an iron concentration of 0.1 to 0.5 millimoles per liter, a molar ratio of iron (III) to oxalate of 1;

1 to 1;

7200 and an oxalate concentration of at least 0.3 millimoles per liter;

b1) exposing an aliquot of the first calibration liquid to light of sufficient wavelength, intensity and duration to convert the oxalate substantially completely to carbon dioxide without affecting the oxygen partial pressure;

c1) conveying the exposed aliquot of first calibration liquid to a measuring chamber for contact with measuring elements for partial pressure of oxygen and of carbon dioxide;

d1) making a measurement with the measuring elements on the exposed aliquot of first calibration liquid;

b2) exposing an aliquot of the second calibration liquid to light of sufficient wavelength, intensity and duration to convert the ferrioxalate substantially completely to carbon dioxide with a concombitant reduction of oxygen partial pressure;

c2) conveying the exposed aliquot of second calibration liquid to the measuring chamber for contact with the measuring elements for the partial pressures of oxygen and carbon dioxide;

d2) making measurements with the measuring elements on the exposed aliquot of second calibration liquid;

e) conveying a liquid sample having analyte values for the partial pressures of oxygen and carbon dioxide into the measuring chamber in contact with the measuring elements for the partial pressures of oxygen and carbon dioxide;

f) making measurements with the measuring elements on the liquid sample; and

g1) comparing the measurements made of oxygen partial pressure with the measuring element therefore on the liquid sample with the measurements made by that measuring element on the aliquots of first and second calibration liquids, and

g2) comparing the measurements made of carbon dioxide partial pressure with the measuring element therefore on the liquid sample with the measurements made by that measuring element on the aliquots of first and second calibration liquids.

18. The method of claim 17 wherein the measuring element for oxygen partial pressure is an electrode and the measuring element for carbon dioxide partial pressure is an electrode.

19. The method of claim 17 wherein the composition of the second calibration liquid is such that the partial pressure of oxygen is zero in the exposed aliquot of second calibration liquid.

20. The method of claim 17 wherein a plurality of liquid samples are subjected to the conveying step (e), making a measurement step (f) and comparing steps (g) (1) and (g) (2), and wherein the first calibration liquid is subjected to the exposing step (b) (1), conveying step (c) (1) and making a measurement step (d) (1) once for the plurality of liquid samples, the comparing steps (g) (1) and (g) (2) for each of the plurality of liquid samples making use of the same values of oxygen and carbon dioxide partial pressure measured in a common measuring step (d) (1).

21. The method of claim 20 wherein a plurality of aliquots of second calibration liquid are subjected to the exposing step (b) (2), conveying step (c) (2) and making a measurement step (d) (2), the comparing steps (g) (1) and (g) (2) for each of the plurality of liquid samples making use of distinct values of oxygen and carbon dioxide partial pressure measured in distinct measuring steps (d) (2).