Process and apparatus for measuring the concentration of a molecule of selective spectrum in a sample substance

• US 4,178,102 A
• Filed: 09/20/1977
• Issued: 12/11/1979
• Est. Priority Date: 09/20/1977
• Status: Expired due to Term

• Current Assignee: US Philips Corporation (Koninklijke Philips N.V.)
• Original Assignee: US Philips Corporation (Koninklijke Philips N.V.)
• Inventors: Riccardi, Clemente C., Meda, Sergio, Cigognini, Luciano
• Primary Examiner(s): McGraw, Vincent P.
• Application Number:
  US05/834,956
• Time in Patent Office: 812 Days
• Field of Search: 356/85, 356/82, 356/75, 356/301, 356/307, 356/317, 356/318, 250/458, 250/459
• US Class Current: 356/307
• CPC Class Codes: G01N 2021/6419 Excitation at two or more wavelengths
• CPC Class Codes: G01N 21/274 Calibration, base line adjustment, drift correction
• 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 21/645 Specially adapted constructive features of fluorimeters

Abstract

A method and apparatus are described for measuring the concentration of a molecule of selective spectrum in a sample substance in which errors from spurious light signals due to diffused light or from spurious fluorescent or phosphorescent light due to traces of other molecules in the sample substance are eliminated. The invention subjects the sample substance to light of a first wavelength in the absorption spectrum of the molecule to be measured and obtains a signal representative of light emission from the molecule with the spurious light signals superimposed thereon. Thereafter, the sample substance is subjected to a second excitation light having a wavelength close to the first wavelength but outside of the absorption and emission spectra of the molecule to be measured to generate a second signal representative of light emission from the molecule to be measured, which light emission results only from diffusion light and/or fluorescent or phosphorescent light due to traces of other molecules in the sample substance. A differentiator then generates a signal of the difference of the first and second signals, which is representative of the true light emission signal of the molecule to be measured.

Claims

1. A process for measuring the concentration of a molecule of selective spectrum in a sample substance, comprising subjecting the sample substance to a first monochromatic excitation light of wavelength lying within the absorption spectrum of the molecule under measurement, filtering and collecting a first light emission from the sample substance at a wavelength lying within the emission spectrum of the molecule, and determining the intensity of the monochromatic light collected, and further comprising subsequently subjecting the sample substance to a second monochromatic excitation light of a wavelength close to that of the first monochromatic light but outside the absorption and emission spectra of the molecule, filtering and collecting a corresponding second light emission from the sample substance at the same wavelength as the first, then determining the new intensity of collected light and subtracting this from the first to give a useful monochromatic light signal free from spurious signals due to diffused light or to spurious fluorescent or phosphorescent light due to traces of other molecules in the sample substance.

2. A process as claimed in claim 1, wherein said secondmonochromatic excitation light has a wavelength lying between the absorption and emission spectra of the molecule.

3. A process as claimed in claim 1, wherein said second monochromatic excitation light has a wavelength greater than those within the emission spectrum of the molecule.

4. A process as claimed in claim 1, comprising a time interval of approximately 0.1-10 μ

sec between the first and second monochromatic excitation light.

5. An apparatus for measuring the concentration of a molecule of selective spectrum in a sample substance, comprising an excitation monochromator arranged to subject the sample substance to a first and subsequently to a second monochromatic excitation light of wavelengths which are close together but which are within the absorption spectrum of the molecule being measured and outside the absorption and emission spectra of the same molecule respectively, a collection monochromator arranged to filter and collect corresponding light emissions from the sample substance at a wavelength within the molecule emission spectrum, and electronic processing means arranged to determine the collected light intensities corresponding to said emissions and subtract one from the other.

6. An apparatus as claimed in claim 5, wherein said collection monochromator comprises a narrow band inlet filter and a photomultiplier arranged to amplify and convert the light intensities emitted by the sample substance and filtered through said inlet filter into corresponding electrical emitted light signals.

7. An apparatus fo measuring the concentration of a molecule of selective spectrum in a sample substance, comprising an excitation monochromator arranged to subject the sample substance to a first and subsequently to a second monochromatic excitation light at wavelengths which are close together but which are within the absorption spectrum of the molecule being measured and outside the absorption and emission spectra of the same molecule respectively, a collection monochromator arranged for filtering and collecting corresponding light emissions from the sample substance at a wavelength within the molecule emission spectrum, and electronic processing means arranged for determining collected light intensities corresponding to said emissions and subtracting one from the other, wherein said electronic processing means comprise memory means for memorizing electrical signals representing the excitation light intensities of said corresponding light emissions, signal normalising means arranged to compare said electrical signals for generating normalised signals insensitive to variations in excitation light intensity, integrator divider means arranged for taking the mean of said normalised signals produced from the first monochromatic excitation light and of the normalised signals produced subsequently by the second monochromatic excitation light, and differentiator means arranged to subtract the mean signal produced by the second monochromatic excitation light from the mean signal produced by the first monochromatic excitation light for generating a single signal constituting the useful monochromatic light signal emitted by the molecule under examination.

8. An apparatus as claimed in claim 7, wherein said collection monochromator comprises a narrow band inlet filter and a photomultiplier arranged to amplify and convert the light intensities emitted by the sample substance and filtered through said inlet filter into said corresponding electrical emitted light signals.