Determination of light absorption pathlength in a vertical-beam photometer

• US 6,995,844 B2
• Filed: 12/10/2002
• Issued: 02/07/2006
• Est. Priority Date: 12/23/1998
• Status: Expired due to Term

• Current Assignee: Molecular Devices
• Original Assignee: Molecular Devices
• Inventors: Hafeman, Dean G., Chow, Calvin Y.
• Primary Examiner(s): Pham, Hoa Q.
• Application Number:
  US10/316,707
• Publication Number:
  US 20030160961A1
• Time in Patent Office: 1,155 Days
• Field of Search: 356432-444, 356319-320, 356418-419, 250/343, 250/344, 250/373, 250/339.05, 250/339.12
• US Class Current: 356/433
• CPC Class Codes: G01J 3/08 Beam switching arrangements
• CPC Class Codes: G01J 3/1804 Plane gratings
• CPC Class Codes: G01N 21/253 for batch operation, i.e. multisample apparatus analytical automats G01N35/00
• CPC Class Codes: G01N 21/31 Investigating relative effect of material at wavelengths characteristic of specific elements or molecules, e.g. atomic absorption spectrometry G01N21/72 takes precedence
• CPC Class Codes: G01N 21/314 with comparison of measurements at specific and non-specific wavelengths dual wavelength spectrometry G01J3/427
• CPC Class Codes: G01N 21/6452 Individual samples arranged in a regular 2D-array, e.g. multiwell plates

Abstract

Disclosed are photometric methods and devices for determining optical pathlength of liquid samples containing analytes dissolved or suspended in a solvent. The methods and devices rely on determining a relationship between the light absorption properties of the solvent and the optical pathlength of liquid samples containing the solvent. This relationship is used to establish the optical pathlength for samples containing an unknown concentration of analyte but having similar solvent composition. Further disclosed are methods and devices for determining the concentration of analyte in such samples where both the optical pathlength and the concentration of analyte are unknown. The methods and devices rely on separately determining, at different wavelengths of light, light absorption by the solvent and light absorption by the analyte. Light absorption by the analyte, together with the optical pathlength so determined, is used to calculate the concentration of the analyte. Devices for carrying out the methods particularly advantageously include vertical-beam photometers containing samples disposed within the wells of multi-assay plates, wherein the photometer is able to monitor light absorption of each sample at multiple wavelengths, including in the visible or UV-visible region of the spectrum, as well as in the near-infrared region of the electromagnetic spectrum. Novel photometer devices are described which automatically determine the concentration of analytes in such multi-assay plates directly without employing a standard curve.

Claims

1. A multi-channel photometric analysis system for determining optical characteristics of analytes in sets of liquid samples containing water and analyte, the system comprising:

a sample holder for holding the sets of samples in one or more substantially vertical optical channels, wherein the samples have unknown optical pathlengths and absorbances;

a light source which transmits light substantially vertically through the samples, wherein the light comprises a calibration wavelength and an analyte-measuring wavelength, wherein the calibration wavelength is within the near infrared wavelength region of from 750–

2500 nanometers and provides a calibration light signal value for each sample, wherein the calibration light signal values are related to the absorption of the water in the samples and the optical pathlengths through the samples and wherein the analyte-measuring wavelength provides an analyte light signal value related to the concentration of analyte present in each sample;

a detector for determining measured light signal values from light transmitted through each sample at the calibration wavelength and the analyte-measuring wavelength;

a means for determining from the calibration light signal values correction factors related to the optical pathlength through each sample;

a means for determining from the correction factors and the analyte light signal values, ratios relating the analyte signal values to the optical pathlength through each sample.

2. The system of claim 1 wherein the correction factor utilizes measurement of light passed through a reference sample of known pathlength.

3. The system of claim 1 wherein the pathlength is determined from a blank corrected water absorbance value at the calibration wavelength.

4. The system of claim 1 wherein light is passed through the sample in the vertical direction through the air liquid interface of the sample.

5. The system of claim 1 wherein the light is passed through the sample and not through the air liquid interface.

6. The system of claim 1 wherein the absorbance of the analyte is negligible at the calibration wavelength.

7. The system of claim 6 wherein the analyte absorbance at the calibration wavelength is less than 0.05.

8. The system of claim 1 wherein the absorbance of the analyte is negligible in the near infrared wavelength region.

9. The system of claim 8 wherein the analyte absorbance in the near infrared wavelength region is less than 0.05.

10. The system of claim 9 wherein an Interference Parameter is determined as follows:

$\mathrm{Interference}<br><br><br><br>\mathrm{Parameter}=\frac{\mathrm{Sample}<br><br><br><br>A_x<br><br>\left[\mathrm{Reference}<br><br><br><br>\left(A_{970}-A_{900}\right)-\mathrm{Solvent}<br><br><br><br>\left(A_{970}-A_{900}\right)\right]}{\mathrm{Reference}<br><br><br><br>A_x<br><br>\left[\mathrm{Sample}<br><br><br><br>\left(A_{970}-A_{900}\right)\right]}$

and the Interference Parameter is between 0.05 and −

0.05.

11. The system of claim 1 wherein an Interference Parameter is determined as follows:

$\mathrm{Interference}<br><br><br><br>\mathrm{Parameter}=\frac{\mathrm{Sample}<br><br><br><br>A_x<br><br>\left[\mathrm{Reference}<br><br><br><br>\left(A_{970}-A_{900}\right)-\mathrm{Solvent}<br><br><br><br>\left(A_{970}-A_{900}\right)\right]}{\mathrm{Reference}<br><br><br><br>A_x<br><br>\left[\mathrm{Sample}<br><br><br><br>\left(A_{970}-A_{900}\right)\right]}$

and the Interference Parameter is between 0.05 and −

0.05.

12. A method of determining optical characteristics of analytes in sets of liquid samples containing water and analyte utilizing a multi-channel photometric analysis device, the device comprising:

holding sets of samples in one or more substantially vertical optical channels, wherein the samples have unknown optical pathlengths and absorbances;

transmitting light substantially vertically through the samples, wherein the transmitted light comprises a calibration wavelength and an analyte-measuring wavelength, wherein the calibration wavelength is within the near infrared wavelength region of from 750–

2500 nanometers and provides a calibration light signal value for each sample, wherein the calibration light signal values are related to the absorption of the water in the samples and the optical pathlengths through the samples and wherein the analyte-measuring wavelength provides an analyte tight signal value related to the concentration of analyte present in each sample;

determining measured light signal values from light transmitted through each sample at the calibration wavelength and the analyte-measuring wavelength;

determining from the calibration light signal values correction factors related to the optical pathlength through each sample;

determining from the correction factors and the analyte light signal values, ratios relating the analyte signal values to the optical pathlength through each sample.

13. The method of claim 12 wherein the correction factor utilizes measurement of light passed through a reference sample of known pathlength.

14. The method of claim 12 wherein the pathlength is determined from a blank corrected water absorbance value for two different wavelengths.

15. The method of claim 12 wherein light is passed through the sample in the vertical direction through the air liquid interface of the sample.

16. The method of claim 12 wherein the light is passed through the sample and not through the air liquid interface.

17. The system of claim 12 wherein the absorbance of the analyte is negligible at the calibration wavelength.

18. The system of claim 17 wherein the analyte absorbance at the calibration wavelength is less than 0.05.

19. The system of claim 12 wherein the absorbance of the analyte is negligible in the near infrared region.

20. The system of claim 19 wherein the analyte absorbance in the near infrared wavelength region is less than 0.05.

21. The system of claim 19 wherein an Interference Parameter is determined as follows:

$\mathrm{Interference}<br><br><br><br>\mathrm{Parameter}=\frac{\mathrm{Sample}<br><br><br><br>A_x<br><br>\left[\mathrm{Reference}<br><br><br><br>\left(A_{970}-A_{900}\right)-\mathrm{Solvent}<br><br><br><br>\left(A_{970}-A_{900}\right)\right]}{\mathrm{Reference}<br><br><br><br>A_x<br><br>\left[\mathrm{Sample}<br><br><br><br>\left(A_{970}-A_{900}\right)\right]}$

and the Interference Parameter is between 0.05 and −

0.05.

22. The system of claim 12 wherein an Interference Parameter is determined as follows:

$\mathrm{Interference}<br><br><br><br>\mathrm{Parameter}=\frac{\mathrm{Sample}<br><br><br><br>A_x<br><br>\left[\mathrm{Reference}<br><br><br><br>\left(A_{970}-A_{900}\right)-\mathrm{Solvent}<br><br><br><br>\left(A_{970}-A_{900}\right)\right]}{\mathrm{Reference}<br><br><br><br>A_x<br><br>\left[\mathrm{Sample}<br><br><br><br>\left(A_{970}-A_{900}\right)\right]}$

and the Interference Parameter is between 0.05 and −

0.05.